The electrochemical oxidation of 5-hydroxymethylfurfural(HMF) represents a significant avenue for sustainable chemical synthesis, owing to its potential to generate high-value derivatives from biomass feedstocks. Tran...The electrochemical oxidation of 5-hydroxymethylfurfural(HMF) represents a significant avenue for sustainable chemical synthesis, owing to its potential to generate high-value derivatives from biomass feedstocks. Transition metal catalysts offer a cost-effective alternative to precious metals for catalyzing HMF oxidation, with transition bimetallic catalysts emerging as particularly promising candidates. In this review, we delve into the intricate reaction pathways and electrochemical mechanisms underlying HMF oxidation, emphasizing the pivotal role of transition bimetallic catalysts in enhancing catalytic efficiency. Subsequently, various types of transition bimetallic catalysts are explored, detailing their synthesis methods and structural modulation strategies. By elucidating the mechanisms behind catalyst modification and performance enhancement, this review sets the stage for upcoming advancements in the field, ultimately advancing the electrochemical HMF conversion and facilitating the transition towards sustainable chemical production.展开更多
The hydrogen evolution reaction(HER)is a promising way to produce hydrogen,and the use of non-precious metals with an excellent electrochemical performance is vital for this.Carbon-based transition metal catalysts hav...The hydrogen evolution reaction(HER)is a promising way to produce hydrogen,and the use of non-precious metals with an excellent electrochemical performance is vital for this.Carbon-based transition metal catalysts have high activity and stability,which are important in reducing the cost of hydrogen production and promoting the development of the hydrogen production industry.However,there is a lack of discussion regarding the effect of carbon components on the performance of these electrocatalysts.This review of the literature discusses the choice of the carbon components in these catalysts and their impact on catalytic performance,including electronic structure control by heteroatom doping,morphology adjustment,and the influence of self-supporting materials.It not only analyzes the progress in HER,but also provides guidance for synthesizing high-performance carbon-based transition metal catalysts.展开更多
Engineering transition metal compounds(TMCs)catalysts with excellent adsorption-catalytic ability has been one of the most effec-tive strategies to accelerate the redox kinetics of sulfur cathodes.Herein,this review f...Engineering transition metal compounds(TMCs)catalysts with excellent adsorption-catalytic ability has been one of the most effec-tive strategies to accelerate the redox kinetics of sulfur cathodes.Herein,this review focuses on engineering TMCs catalysts by cation doping/anion doping/dual doping,bimetallic/bi-anionic TMCs,and TMCs-based heterostructure composites.It is obvious that introducing cations/anions to TMCs or constructing heterostructure can boost adsorption-catalytic capacity by regulating the electronic structure including energy band,d/p-band center,electron filling,and valence state.Moreover,the elec-tronic structure of doped/dual-ionic TMCs are adjusted by inducing ions with different electronegativity,electron filling,and ion radius,resulting in electron redistribution,bonds reconstruction,induced vacancies due to the electronic interaction and changed crystal structure such as lat-tice spacing and lattice distortion.Different from the aforementioned two strategies,heterostructures are constructed by two types of TMCs with different Fermi energy levels,which causes built-in electric field and electrons transfer through the interface,and induces electron redistribution and arranged local atoms to regulate the electronic structure.Additionally,the lacking studies of the three strategies to comprehensively regulate electronic structure for improving catalytic performance are pointed out.It is believed that this review can guide the design of advanced TMCs catalysts for boosting redox of lithium sulfur batteries.展开更多
Sodium-treated sepiolite(Na Sep)-supported transition metal catalysts(TM/Na Sep;TM = Cu, Fe, Ni, Mn, and Co) were synthesized via a rotary evaporation method. Physicochemical properties of the as-synthesized samples w...Sodium-treated sepiolite(Na Sep)-supported transition metal catalysts(TM/Na Sep;TM = Cu, Fe, Ni, Mn, and Co) were synthesized via a rotary evaporation method. Physicochemical properties of the as-synthesized samples were characterized by means of various techniques, and their catalytic activities for HCHO(0.2%) oxidation were evaluated. Among the samples, Cu/Na Sep exhibited superior performance, and complete HCHO conversion was achieved at 100 ℃(GHSV = 240000 m L/(g·h)). Additionally, the sample retained good catalytic activity during a 42 h stability test. A number of factors, including elevated acidity, the abundance of oxygen species, and favorable low-temperature reducibility, were responsible for the excellent catalytic activity of Cu/Na Sep. According to the results of the in-situ DRIFTS characterization, the HCHO oxidation mechanism was as follows:(i) HCHO was rapidly decomposed into dioxymethylene(DOM) species on the Cu/Na Sep surface;(ii) DOM was then immediately converted to formate species;(iii) the resultant formate species were further oxidized to carbonates;(iv) the carbonate species were eventually converted to CO2 and H2O.展开更多
Over the past decade,the first-principles-aided thermodynamic models have become standard theoretical tools in research on structural stability and evolution of transition-metal heterogeneous catalysts under reaction ...Over the past decade,the first-principles-aided thermodynamic models have become standard theoretical tools in research on structural stability and evolution of transition-metal heterogeneous catalysts under reaction environment.Advances in first-principles-aided thermodynamic models mean it is now possible to enable the operando computational modeling,which provides a deep insight into mechanism behind structural stability and evolution,and paves the way for high-through screening for promising transition-metal heterogeneous catalysts.Here,we briefly review the framework and foundation of first-principles-aided thermodynamic models and highlight its contribution to stability analysis on catalysts and identification of reaction-induced structural evolution of catalyst under reaction environment.The present review is helpful for understanding the ongoing developments of first-principles-aided thermodynamic models,which can be employed to screen high-stability catalysts and predict their structural reconstruction in future rational catalyst design.展开更多
Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordi...Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordinary greenhouse gases(GHGs),leading to various environmental issues.Achieving the green production of ammonia is a great challenge,which has been extensively pursued in the last decade.In this review,the most promising strategy,electrochemical nitrate reduction reaction(e-NO_(3)RR),is comprehensively investigated to give a complete understanding of its development and mechanism and provide guidance for future directions.However,owing to the complex reactions and limited selectivity,a comprehensive understanding of the mechanisms is crucial to further development and commercialization.Moreover,NO_(3)^(-)RR is a promising strategy for simultaneous water treatment and NH_(3)production.A detailed overview of the recent progress in NO_(3)^(-)RR for NH_(3)production with nontransition and transition metal based electrocatalysts is summarized.In addition,critical advanced techniques,future challenges,and prospects are discussed to guide future research on transition metal-based catalysts for commercial NH_(3)synthesis by NO_(3)^(-)reduction.展开更多
Metal oxide supported metal catalysts show promising catalytic performance in many industry-relevant reactions.However,the enhancement of performance is often limited by the insufficient metal/metal oxide interface.In...Metal oxide supported metal catalysts show promising catalytic performance in many industry-relevant reactions.However,the enhancement of performance is often limited by the insufficient metal/metal oxide interface.In this work,we demonstrate a general synthesis of Pt-early transition metal oxide(Pt-MO_(x),M=Ti,Zr,V,and Y)catalysts with rich interfacial sites,which is based on the air-induced surface segregation and oxidation of M in the supported Pt-M alloy catalysts.Systematic characterizations verify the dynamic structural response of Pt-M alloy catalysts to air and the formation of Pt-MO_(x) catalysts with abundant interfacial sites.The prepared Pt-TiO_(x) interfacial catalysts exhibit improved performance in hydrogenation reactions of benzaldehyde,nitrobenzene,styrene,and furfural,as a result of the heterolytic dissociation of H_(2) at Pt-metal oxide interfacial sites.展开更多
Thioetherification between mercaptan and diolefin is an efficient process to remove mercaptans in FCC gasoline at mild condition, during which the selective hydrogenation of diolefin to monoolefin is also expected. He...Thioetherification between mercaptan and diolefin is an efficient process to remove mercaptans in FCC gasoline at mild condition, during which the selective hydrogenation of diolefin to monoolefin is also expected. Here, Si O2 supported transition metal（Fe, Co, Ni, Mo and W） phosphides were tested for the thioetherification of isoprene and butanethiol on a fixed-bed reactor at 120℃ and 1.5 MPa H2, and their structure before and after reaction was characterized by means of XRD, HRTEM, N2 sorption, CO chemisorption, NH3-TPD, XPS and TG. It was found that, among different metal phosphides, Mo P/Si O2 showed the best performance, and the optimal nominal Mo P loading was 25%. Apart from the nature of metal, the density of metal and acid sites determined the catalyst performance. Metal site was mainly responsible for hydrogenation of isoprene, while acid site dominantly contributed to the thioetherification and the polymerization of olefins. Moreover, a balance between metallic and acidic functions is required to arrive at a desired performance. Excessive metal sites or acid sites led to the over-hydrogenation of isoprene or the severe polymerization of olefins, respectively. 25%Mo P/Si O2 was tested for 37 h time on stream, and butanethiol conversion maintained at 100%; although isoprene conversion remarkably decreased, the selectivity to isopentenes exceeded 80% after reaction for 11 h. We suggest that the deactivation of Mo P/Si O2 is mainly ascribed to the butanethiol poisoning and the carbonaceous deposit, especially the former.展开更多
Ultra-high-molecular-weight polyethylene(UHMWPE)plays an important role in many important fields as engineering plastics.In this contribution,a precipitation polymerization strategy is developed by combination of high...Ultra-high-molecular-weight polyethylene(UHMWPE)plays an important role in many important fields as engineering plastics.In this contribution,a precipitation polymerization strategy is developed by combination of highly active phosphino-phenolate nickel catalysts with polymer-insoluble solvent(heptane)to access UHMWPE(Mn up to 8.3×10^(6)g mol^(-1))with good product morphology,free-flowing characteristics,and great mechanical properties.Compared with the academically commonly used aromatic solvent(toluene),the utilization of heptane offers simultaneous enhancement in important parameters including activity,polymer molecular weight,and catalyst thermal stability.This system can also generate polar functionalized UHMWPE with molecular weight of up to 1.6×10^(6)g mol^(-1)in the copolymerization of ethylene with polar comonomers.More importantly,this precipitation polymerization strategy is generally applicable to several representative transition metal catalyst systems,leading to UHMWPE synthesis with good product morphology control.展开更多
A new α-diimine ligand 1a, bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene and its corresponding Ni（II） complex 2a, {bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene}d...A new α-diimine ligand 1a, bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene and its corresponding Ni（II） complex 2a, {bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene}dibromo- nickel were successfully synthesized, and characterized by 1H NMR, 13C NMR, Fourier transform infrared spectroscope（FTIR）, elemental analysis and X-ray photoelectron spectroscopy（XPS）. α-Diimine ligand 1b, bis[N,N′-（2,6- dimethylphenyl）imino]-2,3-butanediylidene and its corresponding Ni（II） complex 2b, {bis[N,N′-（2,6-dimethyl- phenyl）imino]-2,3-butanediylidene}dibromonickel were also synthesized and characterized for comparison. The pre-catalyst 2a with sterically bulky, electron-donating group tert-butyl, activated by diethylaluminum chloride （DEAC） and tested in the polymerization of ethylene, was very highly active[2.01×107 g PE/（mol Ni？h？0.1 MPa）] and led to a very highly branched polyethylene（ca. 35―103 branches/1000 C）. The state of the polyethylene obtained varied from plastic, elastomer polymers to the oil-like hyperbranched polymers.展开更多
The electrochemical oxygen reduction reaction(ORR)is pivotal in energy conversion via a 4e-ORR pathway and green hydrogen peroxide production via 2e-ORR pathway.Transition metal single atom catalysts(TM SACs)have attr...The electrochemical oxygen reduction reaction(ORR)is pivotal in energy conversion via a 4e-ORR pathway and green hydrogen peroxide production via 2e-ORR pathway.Transition metal single atom catalysts(TM SACs)have attracted intense attention in recent years for ORR due to their high activity and near maximum metal atom utilization.The future development of TM SACs for ORR requires improved understanding of reaction pathways,since currently the true origin of activity remains contentious owing to the lack of qualitative/quantitative information about active sites.Knowledge-guided design is imperative for the optimization of TM SACs performance in terms of activity and selectivity.This review focuses on the latest progress in the design of TM SACs for ORR,placing particular attention on efforts to elucidate reaction mechanisms.Experimental evidence based on in-situ/operando characterization measurements,along with theoretical predictions,are summarized to deepen understanding of the structure-performance relationships at both atomic and molecular level.Finally,some perspectives are offered relating to the fundamental science needed for TM SACs to find practical application in energy storage and conversion devices.We hope this review will inspire the development of new synthetic routes towards high-performance ORR electrocatalysts for the energy sector.展开更多
Non-noble metal catalysts are suitable for the oxygen evolution reaction(OER)owing to their original oxidation states and oxygen coordination environments,which can regulate the adsorption of OH−at the active sites to...Non-noble metal catalysts are suitable for the oxygen evolution reaction(OER)owing to their original oxidation states and oxygen coordination environments,which can regulate the adsorption of OH−at the active sites to facilitate the formation of oxygencontaining intermediates.However,the difficulties encountered in the conversion of intermediates(M–OH,M–O,and M–OOH)lead to low efficiency.Decorations of transition metal catalysts with foreign elements are regarded effective solutions,among which decoration with Ce-based materials(CeBM)is the most prominent.This review investigates the current status and future prospects of CeBM-decorated transition metal electrocatalysts.By presenting a thorough account of the latest development,we aim to set a common ground for the research community for a deeper understanding of the roles of CeBM that originate from its unique electronic structure and abundant oxygen vacancies.Moreover,we wish to provide our own perspectives as to how to further the design of Ce-based OER electrocatalysts and where such catalysts may be applied in fields beyond electrocatalysis.展开更多
Acceptorless dehydrogenation (AD) that uses non-toxic reagents and produces no waste is a type of catalytic reactions toward green chemistry. Acceptorless alcohol dehydrogenation (AAD) can serve as a key step in const...Acceptorless dehydrogenation (AD) that uses non-toxic reagents and produces no waste is a type of catalytic reactions toward green chemistry. Acceptorless alcohol dehydrogenation (AAD) can serve as a key step in constructing new bonds such as C-C and C-N bonds in which alcohols need to be activated into more reactive ketones or aldehydes. AD reactions also can be utilized for hydrogen production from biomass or its fermentation products (mainly alcohols). Reversible hydrogenation/ dehy-drogenation with hydrogen uptake/release is crucial to realization of the potential organic hydride hydrogen storage. In this article, we review the recent computational mechanistic studies of the AD reactions catalyzed by various transition metal complexes as well as the experimental developments. These reactions include acceptorless alcohol dehydrogenations, reversible dehydrogenation/hydrogenation of nitrogen heterocycles, dehydrogenative coupling reactions of alcohols and amines to construct C-N bonds, and dehydrogenative coupling reactions of alcohols and unsaturated substrates to form C-C bonds. For the catalysts possessing metal-ligand bifunctional active sites (such as 28, 45, 86, 87, and 106 in the paper), the dehydrogenations prefer the "bifunctional double hydrogen transfer" mechanism rather than the generally accepted-H elimination mechanism. However, methanol dehydrogenation involved in the C-C coupling reaction of methanol and allene, catalyzed by the iridium complex 121, takes place via the-H elimination mechanism, because the Lewis basicity of either the-allyl moiety or the carboxyl group of the ligand is too weak to exert high Lewis basic reactivity. Unveiling the catalytic mechanisms of AD reactions could help to develop new catalysts.展开更多
Critical limitations in applying MgH_(2) as a hydrogen-storage medium include the high H_(2) desorption temperature and slow reaction kinetics.In this study,we synthesized hierarchical porous TiNb_(2)O_(7) spheres in ...Critical limitations in applying MgH_(2) as a hydrogen-storage medium include the high H_(2) desorption temperature and slow reaction kinetics.In this study,we synthesized hierarchical porous TiNb_(2)O_(7) spheres in micrometer scale built with 20-50 nm nanospheres,which showed stable activity to catalyze hydrogen storage in MgH_(2) as precursors.The addition of 7 wt.%TiNb_(2)O_(7) in MgH_(2) reduced the dehydrogenation onset temperature from 300 to 177℃.At 250℃,approximately 5.5 wt.%H_(2) was rapidly released in 10 min.Hydrogen uptake was detected even at room temperature under 50 bar hydrogen;4.5 wt.%H_(2) was absorbed in 3 min at 150℃,exhibiting a superior low-temperature hydrogenation performance.Moreover,nearly constant capacity was observed from the second cycle onward,demonstrating stable cyclability.During the ball milling and initial de/hydrogenation process,the high-valent Ti and Nb of TiNb_(2)O_(7) were reduced to the lower-valent species or even zero-valent metal,which in situ created multivalent multielement catalytic surroundings.A strong synergistic effect was obtained for hybrid oxides of Nb and Ti by density functional theory(DFT)calculations,which largely weakens the Mg-H bonding and results in a large reduction in kinetic barriers for hydrogen storage reactions of MgH_(2).Our findings may guide the further design and development of high-performance complex catalysts for the reversible hydrogen storage of hydrides.展开更多
To address the issue of hemilabile catalyst in olefin polymerization catalysis, a cyclizing strategy was used to construct novel N-bridged phosphine-carbonyl palladium and nickel catalysts, resulting in improvements o...To address the issue of hemilabile catalyst in olefin polymerization catalysis, a cyclizing strategy was used to construct novel N-bridged phosphine-carbonyl palladium and nickel catalysts, resulting in improvements on ethylene(co)polymerizations. The N-bridged phosphinecarbonyl Pd catalysts(Pd1-Pd5) and Ni catalysts(Ni1-Ni5) bearing five-to eight-membered-ring structures were designed and synthesized.Catalytic performance for ethylene(co)polymerization became better as the size of N-containing bridge increased. The seven-membered-ring bridged catalysts Pd4 and Ni4 exhibited the best performance in terms of catalytic activity, polymer molecular weight and incorporation of acrylates and acrylic acid. The better performance of these catalysts bearing larger-size bridges was tentatively attributed to the methyleneinduced higher electron density around nitrogen, which strenghtens the coordination of carbonyl group to metal center, and also to the steric effect offered by this cyclization. This work provides a new strategy to enhance hemilabile polymerization catalysts.展开更多
The electrocatalysis reactions involving oxygen,such as oxygen evolution reaction(OER)and oxygen reduction reaction(ORR),play a critical role in energy storage/conversion applications,e.g.,fuel cells,metal-air batteri...The electrocatalysis reactions involving oxygen,such as oxygen evolution reaction(OER)and oxygen reduction reaction(ORR),play a critical role in energy storage/conversion applications,e.g.,fuel cells,metal-air batteries,and electrochemical water splitting.The high kinetic energy barrier of the OER/ORR is highly associated with the spin state interconversion between singlet OH^(−)/H_(2)O and triplet O_(2),which is influenced by the spin state and magnetism of catalysts.This Review summarizes recent progress and advances in understanding spin/magnetism-related effects in oxygen electrocatalysis to develop spin theory.It is demonstrated that the spin states(low,intermediate,and high spin)of magnetic transition metal catalysts(TMCs)can directly affect the reaction barriers of OER/ORR by tailoring the bonding of oxygen intermediates with TMCs.Besides,the spin states of TMCs can build a spin-selective channel to filter the electron spins required for the single/triplet interconversion of O species during OER/ORR.In this Review,we introduced many approaches to modulating spin state,for instance,altering the crystal field,oxidation state of active-site ions,and the morphology of TMCs.What’s more,a magnetic field can drive the spin flip of magnetic ions to achieve the spin alignment(↑↑)(i.e.,facilitating spin polarization),which will strengthen the spin selectivity for accelerating the filtration and transfer of the spins with the same direction for the generation and conversion of triplet ↑O=O↑.Importantly,the origin of magnetic field enhancement on OER/ORR are deeply discussed,which provides a great vision for the magnetism-assisted catalysis.Finally,the challenges and perspectives for future development of spin/magnetism catalysis are presented.This Review is expected to highlight the significance of spin/magnetism theory in breaking the bottleneck of electrocatalysis field and promote the development of high-efficientcy electrocatalysts for practical applications.展开更多
Two types of salicylaldiminato-based nickel complexes,mono-ligated Ni(II)complexes([O-C_(6)H_(4)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(5),[O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(6),[O-(3-t-Bu)C_(6)H_(3)-o-C(H)=N-A...Two types of salicylaldiminato-based nickel complexes,mono-ligated Ni(II)complexes([O-C_(6)H_(4)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(5),[O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(6),[O-(3-t-Bu)C_(6)H_(3)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(7))and bis-ligated Ni(II)complexes([O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-Ar]_(2)Ni(8),[O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-2-C_(6)H_(4)(PhO)]_(2)Ni(9),Ar=2,6-C_(6)H_(3)(i-Pr)_(2))were synthesized and characterized by Fourier transform infrared spectroscopy(FT-IR),nuclear magnetic resonance(NMR),mass spectrography(MS)and elemental analysis(EA).In the presence of methylaluminoxane(MAO)as cocatalyst,all the nickel complexes exhibited high activities for the polymerization of methyl methacrylate(MMA)and syndiotactic-rich poly(methyl methacrylate)(PMMA)was obtained.The complexes with less bulky substituents on salicylaldiminato framework possessed higher activities,while with the same salicylaldiminato,the mono-ligated nickel complexes showed higher catalytic activity than bis-ligated ones.展开更多
基金Hubei Provincial Natural Science Foundation of China (2023AFB0049)Scientific Research Fund Project of Wuhan Institute of Technology (K202232 and K2023028)Graduate Education Innovation Fund of Wuhan Institute of Technology (CX2023091)。
文摘The electrochemical oxidation of 5-hydroxymethylfurfural(HMF) represents a significant avenue for sustainable chemical synthesis, owing to its potential to generate high-value derivatives from biomass feedstocks. Transition metal catalysts offer a cost-effective alternative to precious metals for catalyzing HMF oxidation, with transition bimetallic catalysts emerging as particularly promising candidates. In this review, we delve into the intricate reaction pathways and electrochemical mechanisms underlying HMF oxidation, emphasizing the pivotal role of transition bimetallic catalysts in enhancing catalytic efficiency. Subsequently, various types of transition bimetallic catalysts are explored, detailing their synthesis methods and structural modulation strategies. By elucidating the mechanisms behind catalyst modification and performance enhancement, this review sets the stage for upcoming advancements in the field, ultimately advancing the electrochemical HMF conversion and facilitating the transition towards sustainable chemical production.
文摘The hydrogen evolution reaction(HER)is a promising way to produce hydrogen,and the use of non-precious metals with an excellent electrochemical performance is vital for this.Carbon-based transition metal catalysts have high activity and stability,which are important in reducing the cost of hydrogen production and promoting the development of the hydrogen production industry.However,there is a lack of discussion regarding the effect of carbon components on the performance of these electrocatalysts.This review of the literature discusses the choice of the carbon components in these catalysts and their impact on catalytic performance,including electronic structure control by heteroatom doping,morphology adjustment,and the influence of self-supporting materials.It not only analyzes the progress in HER,but also provides guidance for synthesizing high-performance carbon-based transition metal catalysts.
基金The authors acknowledge funding from National Natural Science Foundation of China(52302307)Shaanxi Province(2023-ZDLGY-24,2023-JC-QN-0473)+2 种基金project funded by China Postdoctoral Science Foundation(2023MD734210)the Open Foundation of State Key Laboratory for Advanced Metals and Materials(2022-Z01)Shaanxi Provincial Department of Education industrialization project(21JC018).
文摘Engineering transition metal compounds(TMCs)catalysts with excellent adsorption-catalytic ability has been one of the most effec-tive strategies to accelerate the redox kinetics of sulfur cathodes.Herein,this review focuses on engineering TMCs catalysts by cation doping/anion doping/dual doping,bimetallic/bi-anionic TMCs,and TMCs-based heterostructure composites.It is obvious that introducing cations/anions to TMCs or constructing heterostructure can boost adsorption-catalytic capacity by regulating the electronic structure including energy band,d/p-band center,electron filling,and valence state.Moreover,the elec-tronic structure of doped/dual-ionic TMCs are adjusted by inducing ions with different electronegativity,electron filling,and ion radius,resulting in electron redistribution,bonds reconstruction,induced vacancies due to the electronic interaction and changed crystal structure such as lat-tice spacing and lattice distortion.Different from the aforementioned two strategies,heterostructures are constructed by two types of TMCs with different Fermi energy levels,which causes built-in electric field and electrons transfer through the interface,and induces electron redistribution and arranged local atoms to regulate the electronic structure.Additionally,the lacking studies of the three strategies to comprehensively regulate electronic structure for improving catalytic performance are pointed out.It is believed that this review can guide the design of advanced TMCs catalysts for boosting redox of lithium sulfur batteries.
文摘Sodium-treated sepiolite(Na Sep)-supported transition metal catalysts(TM/Na Sep;TM = Cu, Fe, Ni, Mn, and Co) were synthesized via a rotary evaporation method. Physicochemical properties of the as-synthesized samples were characterized by means of various techniques, and their catalytic activities for HCHO(0.2%) oxidation were evaluated. Among the samples, Cu/Na Sep exhibited superior performance, and complete HCHO conversion was achieved at 100 ℃(GHSV = 240000 m L/(g·h)). Additionally, the sample retained good catalytic activity during a 42 h stability test. A number of factors, including elevated acidity, the abundance of oxygen species, and favorable low-temperature reducibility, were responsible for the excellent catalytic activity of Cu/Na Sep. According to the results of the in-situ DRIFTS characterization, the HCHO oxidation mechanism was as follows:(i) HCHO was rapidly decomposed into dioxymethylene(DOM) species on the Cu/Na Sep surface;(ii) DOM was then immediately converted to formate species;(iii) the resultant formate species were further oxidized to carbonates;(iv) the carbonate species were eventually converted to CO2 and H2O.
基金supported by the National Natural Science Foundation of China(Grant Nos.21822801)China Postdoctoral Science Foundation(2019TQ0021)the Fundamental Research Funds for the Central Universities(XK18021 and XK180301)。
文摘Over the past decade,the first-principles-aided thermodynamic models have become standard theoretical tools in research on structural stability and evolution of transition-metal heterogeneous catalysts under reaction environment.Advances in first-principles-aided thermodynamic models mean it is now possible to enable the operando computational modeling,which provides a deep insight into mechanism behind structural stability and evolution,and paves the way for high-through screening for promising transition-metal heterogeneous catalysts.Here,we briefly review the framework and foundation of first-principles-aided thermodynamic models and highlight its contribution to stability analysis on catalysts and identification of reaction-induced structural evolution of catalyst under reaction environment.The present review is helpful for understanding the ongoing developments of first-principles-aided thermodynamic models,which can be employed to screen high-stability catalysts and predict their structural reconstruction in future rational catalyst design.
基金supported by the National Natural Science Foundation of China(Grant Nos.22050410268,22176131)Shenzhen Basic Research General Project(JCYJ20210324095205015,JCYJ20220818095601002)。
文摘Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordinary greenhouse gases(GHGs),leading to various environmental issues.Achieving the green production of ammonia is a great challenge,which has been extensively pursued in the last decade.In this review,the most promising strategy,electrochemical nitrate reduction reaction(e-NO_(3)RR),is comprehensively investigated to give a complete understanding of its development and mechanism and provide guidance for future directions.However,owing to the complex reactions and limited selectivity,a comprehensive understanding of the mechanisms is crucial to further development and commercialization.Moreover,NO_(3)^(-)RR is a promising strategy for simultaneous water treatment and NH_(3)production.A detailed overview of the recent progress in NO_(3)^(-)RR for NH_(3)production with nontransition and transition metal based electrocatalysts is summarized.In addition,critical advanced techniques,future challenges,and prospects are discussed to guide future research on transition metal-based catalysts for commercial NH_(3)synthesis by NO_(3)^(-)reduction.
基金support from the National Natural Science Foundation of China(Nos.22221003 and 22071225)the Plan for Anhui Major Provincial Science&Technology Project(Nos.202203a0520013 and 2021d05050006)the fellowship of China Postdoctoral Science Foundation(No.2022M712179).
文摘Metal oxide supported metal catalysts show promising catalytic performance in many industry-relevant reactions.However,the enhancement of performance is often limited by the insufficient metal/metal oxide interface.In this work,we demonstrate a general synthesis of Pt-early transition metal oxide(Pt-MO_(x),M=Ti,Zr,V,and Y)catalysts with rich interfacial sites,which is based on the air-induced surface segregation and oxidation of M in the supported Pt-M alloy catalysts.Systematic characterizations verify the dynamic structural response of Pt-M alloy catalysts to air and the formation of Pt-MO_(x) catalysts with abundant interfacial sites.The prepared Pt-TiO_(x) interfacial catalysts exhibit improved performance in hydrogenation reactions of benzaldehyde,nitrobenzene,styrene,and furfural,as a result of the heterolytic dissociation of H_(2) at Pt-metal oxide interfacial sites.
基金supported by the State Key Laboratory of Catalytic Materials and Reaction Engineering(RIPP,SINOPEC)
文摘Thioetherification between mercaptan and diolefin is an efficient process to remove mercaptans in FCC gasoline at mild condition, during which the selective hydrogenation of diolefin to monoolefin is also expected. Here, Si O2 supported transition metal（Fe, Co, Ni, Mo and W） phosphides were tested for the thioetherification of isoprene and butanethiol on a fixed-bed reactor at 120℃ and 1.5 MPa H2, and their structure before and after reaction was characterized by means of XRD, HRTEM, N2 sorption, CO chemisorption, NH3-TPD, XPS and TG. It was found that, among different metal phosphides, Mo P/Si O2 showed the best performance, and the optimal nominal Mo P loading was 25%. Apart from the nature of metal, the density of metal and acid sites determined the catalyst performance. Metal site was mainly responsible for hydrogenation of isoprene, while acid site dominantly contributed to the thioetherification and the polymerization of olefins. Moreover, a balance between metallic and acidic functions is required to arrive at a desired performance. Excessive metal sites or acid sites led to the over-hydrogenation of isoprene or the severe polymerization of olefins, respectively. 25%Mo P/Si O2 was tested for 37 h time on stream, and butanethiol conversion maintained at 100%; although isoprene conversion remarkably decreased, the selectivity to isopentenes exceeded 80% after reaction for 11 h. We suggest that the deactivation of Mo P/Si O2 is mainly ascribed to the butanethiol poisoning and the carbonaceous deposit, especially the former.
基金This work was supported by National Key R&D Program of China(No.2021YFA1501700)National Natural Science Foundation of China(No.52025031,52203016,and 22261142664)USTC Research Funds of the Double First-Class Initiative(YD9990002018).
文摘Ultra-high-molecular-weight polyethylene(UHMWPE)plays an important role in many important fields as engineering plastics.In this contribution,a precipitation polymerization strategy is developed by combination of highly active phosphino-phenolate nickel catalysts with polymer-insoluble solvent(heptane)to access UHMWPE(Mn up to 8.3×10^(6)g mol^(-1))with good product morphology,free-flowing characteristics,and great mechanical properties.Compared with the academically commonly used aromatic solvent(toluene),the utilization of heptane offers simultaneous enhancement in important parameters including activity,polymer molecular weight,and catalyst thermal stability.This system can also generate polar functionalized UHMWPE with molecular weight of up to 1.6×10^(6)g mol^(-1)in the copolymerization of ethylene with polar comonomers.More importantly,this precipitation polymerization strategy is generally applicable to several representative transition metal catalyst systems,leading to UHMWPE synthesis with good product morphology control.
基金Supported by the National Natural Science Foundation of China(No.20964003)
文摘A new α-diimine ligand 1a, bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene and its corresponding Ni（II） complex 2a, {bis[N,N′-（4-tert-butyl-2,6-dimethylphenyl）imino]-2,3-butanediylidene}dibromo- nickel were successfully synthesized, and characterized by 1H NMR, 13C NMR, Fourier transform infrared spectroscope（FTIR）, elemental analysis and X-ray photoelectron spectroscopy（XPS）. α-Diimine ligand 1b, bis[N,N′-（2,6- dimethylphenyl）imino]-2,3-butanediylidene and its corresponding Ni（II） complex 2b, {bis[N,N′-（2,6-dimethyl- phenyl）imino]-2,3-butanediylidene}dibromonickel were also synthesized and characterized for comparison. The pre-catalyst 2a with sterically bulky, electron-donating group tert-butyl, activated by diethylaluminum chloride （DEAC） and tested in the polymerization of ethylene, was very highly active[2.01×107 g PE/（mol Ni？h？0.1 MPa）] and led to a very highly branched polyethylene（ca. 35―103 branches/1000 C）. The state of the polyethylene obtained varied from plastic, elastomer polymers to the oil-like hyperbranched polymers.
基金This work was financially supported by the National Natural Science Foundation of China(Nos.52122308,51973200,52202050)the China Postdoctoral Science Foundation(2022TQ0286).
文摘The electrochemical oxygen reduction reaction(ORR)is pivotal in energy conversion via a 4e-ORR pathway and green hydrogen peroxide production via 2e-ORR pathway.Transition metal single atom catalysts(TM SACs)have attracted intense attention in recent years for ORR due to their high activity and near maximum metal atom utilization.The future development of TM SACs for ORR requires improved understanding of reaction pathways,since currently the true origin of activity remains contentious owing to the lack of qualitative/quantitative information about active sites.Knowledge-guided design is imperative for the optimization of TM SACs performance in terms of activity and selectivity.This review focuses on the latest progress in the design of TM SACs for ORR,placing particular attention on efforts to elucidate reaction mechanisms.Experimental evidence based on in-situ/operando characterization measurements,along with theoretical predictions,are summarized to deepen understanding of the structure-performance relationships at both atomic and molecular level.Finally,some perspectives are offered relating to the fundamental science needed for TM SACs to find practical application in energy storage and conversion devices.We hope this review will inspire the development of new synthetic routes towards high-performance ORR electrocatalysts for the energy sector.
基金This research was made possible as a result of a generous grant from Shenzhen Nobel Prize Scientists Laboratory Project(grant no.C17213101)Guangdong Provincial Key Laboratory of Catalysis(no.2020B121201002)+1 种基金Guangdong Provincial Key Laboratory of Energy Materials for Electric Power(no.2018B030322001)China Postdoctoral Science Foundation(no.2018M642133).
文摘Non-noble metal catalysts are suitable for the oxygen evolution reaction(OER)owing to their original oxidation states and oxygen coordination environments,which can regulate the adsorption of OH−at the active sites to facilitate the formation of oxygencontaining intermediates.However,the difficulties encountered in the conversion of intermediates(M–OH,M–O,and M–OOH)lead to low efficiency.Decorations of transition metal catalysts with foreign elements are regarded effective solutions,among which decoration with Ce-based materials(CeBM)is the most prominent.This review investigates the current status and future prospects of CeBM-decorated transition metal electrocatalysts.By presenting a thorough account of the latest development,we aim to set a common ground for the research community for a deeper understanding of the roles of CeBM that originate from its unique electronic structure and abundant oxygen vacancies.Moreover,we wish to provide our own perspectives as to how to further the design of Ce-based OER electrocatalysts and where such catalysts may be applied in fields beyond electrocatalysis.
基金supported by the Chinese Academy of Sciencesthe National Natural Science Foundation of China (20973197 and 21173263)
文摘Acceptorless dehydrogenation (AD) that uses non-toxic reagents and produces no waste is a type of catalytic reactions toward green chemistry. Acceptorless alcohol dehydrogenation (AAD) can serve as a key step in constructing new bonds such as C-C and C-N bonds in which alcohols need to be activated into more reactive ketones or aldehydes. AD reactions also can be utilized for hydrogen production from biomass or its fermentation products (mainly alcohols). Reversible hydrogenation/ dehy-drogenation with hydrogen uptake/release is crucial to realization of the potential organic hydride hydrogen storage. In this article, we review the recent computational mechanistic studies of the AD reactions catalyzed by various transition metal complexes as well as the experimental developments. These reactions include acceptorless alcohol dehydrogenations, reversible dehydrogenation/hydrogenation of nitrogen heterocycles, dehydrogenative coupling reactions of alcohols and amines to construct C-N bonds, and dehydrogenative coupling reactions of alcohols and unsaturated substrates to form C-C bonds. For the catalysts possessing metal-ligand bifunctional active sites (such as 28, 45, 86, 87, and 106 in the paper), the dehydrogenations prefer the "bifunctional double hydrogen transfer" mechanism rather than the generally accepted-H elimination mechanism. However, methanol dehydrogenation involved in the C-C coupling reaction of methanol and allene, catalyzed by the iridium complex 121, takes place via the-H elimination mechanism, because the Lewis basicity of either the-allyl moiety or the carboxyl group of the ligand is too weak to exert high Lewis basic reactivity. Unveiling the catalytic mechanisms of AD reactions could help to develop new catalysts.
基金the National Key R&D Program of China(No.2018YFB1502102)the National Natural Science Foundation of China(Nos.51671172,U1601212)the National Youth Top-Notch Talent Support Program.
文摘Critical limitations in applying MgH_(2) as a hydrogen-storage medium include the high H_(2) desorption temperature and slow reaction kinetics.In this study,we synthesized hierarchical porous TiNb_(2)O_(7) spheres in micrometer scale built with 20-50 nm nanospheres,which showed stable activity to catalyze hydrogen storage in MgH_(2) as precursors.The addition of 7 wt.%TiNb_(2)O_(7) in MgH_(2) reduced the dehydrogenation onset temperature from 300 to 177℃.At 250℃,approximately 5.5 wt.%H_(2) was rapidly released in 10 min.Hydrogen uptake was detected even at room temperature under 50 bar hydrogen;4.5 wt.%H_(2) was absorbed in 3 min at 150℃,exhibiting a superior low-temperature hydrogenation performance.Moreover,nearly constant capacity was observed from the second cycle onward,demonstrating stable cyclability.During the ball milling and initial de/hydrogenation process,the high-valent Ti and Nb of TiNb_(2)O_(7) were reduced to the lower-valent species or even zero-valent metal,which in situ created multivalent multielement catalytic surroundings.A strong synergistic effect was obtained for hybrid oxides of Nb and Ti by density functional theory(DFT)calculations,which largely weakens the Mg-H bonding and results in a large reduction in kinetic barriers for hydrogen storage reactions of MgH_(2).Our findings may guide the further design and development of high-performance complex catalysts for the reversible hydrogen storage of hydrides.
基金financial support from the National Natural Science Foundation of China (Nos. 22122110 ad 21871250)the Jilin Provincial Science and Technology Department Program (No. 20200801009GH)Shaanxi Provincial Natural Science Basic Research Program-Shaanxi Coal and Chemical Industry Group Co., Ltd. Joint Fund (No. 2019JLZ-02)。
文摘To address the issue of hemilabile catalyst in olefin polymerization catalysis, a cyclizing strategy was used to construct novel N-bridged phosphine-carbonyl palladium and nickel catalysts, resulting in improvements on ethylene(co)polymerizations. The N-bridged phosphinecarbonyl Pd catalysts(Pd1-Pd5) and Ni catalysts(Ni1-Ni5) bearing five-to eight-membered-ring structures were designed and synthesized.Catalytic performance for ethylene(co)polymerization became better as the size of N-containing bridge increased. The seven-membered-ring bridged catalysts Pd4 and Ni4 exhibited the best performance in terms of catalytic activity, polymer molecular weight and incorporation of acrylates and acrylic acid. The better performance of these catalysts bearing larger-size bridges was tentatively attributed to the methyleneinduced higher electron density around nitrogen, which strenghtens the coordination of carbonyl group to metal center, and also to the steric effect offered by this cyclization. This work provides a new strategy to enhance hemilabile polymerization catalysts.
基金financially supported by the National Natural Science Foundation of China(Grants No.52027801,52111530236)the National Postdoctoral Program for Innovative Talents(BX20220002)China Postdoctoral Science Foundation(2022M720204).
文摘The electrocatalysis reactions involving oxygen,such as oxygen evolution reaction(OER)and oxygen reduction reaction(ORR),play a critical role in energy storage/conversion applications,e.g.,fuel cells,metal-air batteries,and electrochemical water splitting.The high kinetic energy barrier of the OER/ORR is highly associated with the spin state interconversion between singlet OH^(−)/H_(2)O and triplet O_(2),which is influenced by the spin state and magnetism of catalysts.This Review summarizes recent progress and advances in understanding spin/magnetism-related effects in oxygen electrocatalysis to develop spin theory.It is demonstrated that the spin states(low,intermediate,and high spin)of magnetic transition metal catalysts(TMCs)can directly affect the reaction barriers of OER/ORR by tailoring the bonding of oxygen intermediates with TMCs.Besides,the spin states of TMCs can build a spin-selective channel to filter the electron spins required for the single/triplet interconversion of O species during OER/ORR.In this Review,we introduced many approaches to modulating spin state,for instance,altering the crystal field,oxidation state of active-site ions,and the morphology of TMCs.What’s more,a magnetic field can drive the spin flip of magnetic ions to achieve the spin alignment(↑↑)(i.e.,facilitating spin polarization),which will strengthen the spin selectivity for accelerating the filtration and transfer of the spins with the same direction for the generation and conversion of triplet ↑O=O↑.Importantly,the origin of magnetic field enhancement on OER/ORR are deeply discussed,which provides a great vision for the magnetism-assisted catalysis.Finally,the challenges and perspectives for future development of spin/magnetism catalysis are presented.This Review is expected to highlight the significance of spin/magnetism theory in breaking the bottleneck of electrocatalysis field and promote the development of high-efficientcy electrocatalysts for practical applications.
基金sponsored by the Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry of China,the Science and Technology Innovation Program of the China National Petroleum Corporation,and the Key Laboratory of Advanced Polymer Materials of Shanghai(Grant No.08DZ2230500)the Science and Technology Innovation Program of China National Petroleum Corporation.
文摘Two types of salicylaldiminato-based nickel complexes,mono-ligated Ni(II)complexes([O-C_(6)H_(4)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(5),[O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(6),[O-(3-t-Bu)C_(6)H_(3)-o-C(H)=N-Ar]Ni(PPh_(3))(Ph)(7))and bis-ligated Ni(II)complexes([O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-Ar]_(2)Ni(8),[O-(3,5-Br_(2))C_(6)H_(2)-o-C(H)=N-2-C_(6)H_(4)(PhO)]_(2)Ni(9),Ar=2,6-C_(6)H_(3)(i-Pr)_(2))were synthesized and characterized by Fourier transform infrared spectroscopy(FT-IR),nuclear magnetic resonance(NMR),mass spectrography(MS)and elemental analysis(EA).In the presence of methylaluminoxane(MAO)as cocatalyst,all the nickel complexes exhibited high activities for the polymerization of methyl methacrylate(MMA)and syndiotactic-rich poly(methyl methacrylate)(PMMA)was obtained.The complexes with less bulky substituents on salicylaldiminato framework possessed higher activities,while with the same salicylaldiminato,the mono-ligated nickel complexes showed higher catalytic activity than bis-ligated ones.
