A 3D nitrogen⁃doped graphene/multi⁃walled carbon nanotube(CS⁃GO⁃NCNT)crosslinked network mate⁃rial was successfully synthesized utilizing chitosan and melamine as carbon and nitrogen sources,concomitant with the incor...A 3D nitrogen⁃doped graphene/multi⁃walled carbon nanotube(CS⁃GO⁃NCNT)crosslinked network mate⁃rial was successfully synthesized utilizing chitosan and melamine as carbon and nitrogen sources,concomitant with the incorporation of multi⁃wall carbon nanotubes and employing freeze drying technology.The material amalgamates the merits of 1D/2D hybrid carbon materials,wherein 1D carbon nanotubes confer robustness and expedited elec⁃tron transport pathways,while 2D graphene sheets facilitate rapid ion migration.Furthermore,the introduction of nitrogen heteroatoms serves to furnish additional active sites for lithium storage.When served as an anode material for lithium⁃ion batteries,the CS⁃GO⁃NCNT electrode delivered a reversible capacity surpassing 500 mAh·g^(-1),mark⁃edly outperforming commercial graphite anodes.Even after 300 cycles at a high current density of 1 A·g^(-1),it remained a reversible capacity of up to 268 mAh·g^(-1).展开更多
Graphene oxide(GO)with excellent dispersion ability can assist the dispersion of single-walled carbon nanotube(SWCNT)and promote the formation of uniform and stable GO/SWCNT coating liquid.The highly conductive polyet...Graphene oxide(GO)with excellent dispersion ability can assist the dispersion of single-walled carbon nanotube(SWCNT)and promote the formation of uniform and stable GO/SWCNT coating liquid.The highly conductive polyethylene terephthalate/reduced graphene oxide/SWCNT(PET/rGO/SWCNT)electromagnetic shielding composite fabric was successfully prepared by anchoring rGO/SWCNT on PET fabric via dip-coating piror to low-temperature thermal reduction.The results showed that the carboxyl groups and hydroxyl groups formed of hydrophilic-treated PET were conducive to the formation of hydrogen bonds with that of GO,which enhanced the interaction between PET fabric and GO/SWCNT coating;the loading of GO/SWCNT increased with the number of dip-coating,the unit area loading of rGO/SWCNT in the final composite fabric was 2.7 mg/cm^(2) after 10 dip-coating cycles and thermal reduction;the PET/rGO/SWCNT composite fabric had a continuous and dense conductive network,with a conductivity of up to 41.6 S/m and the average electromagnetic interference shielding effectiveness in X-band was 22 dB;the flexible PET/rGO/SWCNT composite fabric was not only easy to process,but also exhibited excellent conductivity and shielding efficiency,showing great potential in the application of electromagnetic shielding fabrics.展开更多
CdSe quantum dots(QDs)hybridized with graphene oxide(GO)are synthesized by a facile chemical precipitation method.The absorption of the CdSe/GO nanocomposite is increased with a significantblue shift with respect to C...CdSe quantum dots(QDs)hybridized with graphene oxide(GO)are synthesized by a facile chemical precipitation method.The absorption of the CdSe/GO nanocomposite is increased with a significantblue shift with respect to CdSe QDs.The specific surface area of the CdSe/GO nanocomposite is10.4m2/g,which is higher than that of CdSe QDs(5m2/g).The PL intensity of the CdSe/GO nanocomposite is lower than that of the CdSe QDs owing to the inhibition of the recombination of electron‐hole pairs in the composite.In Raman analysis,the two bands of the CdSe/GO nanocomposite are shifted to higher wavenumbers with respect to graphene oxide,which is attributed to electron injection that is induced by CdSe QDs into graphene oxide.Using the Brilliant Green dye,the photocatalytic reduction efficiency of CdSe QDs and the CdSe/GO nanocomposite under sunlight irradiation for90min are approximately81.9%and95.5%,respectively.The calculated photodegradation rate constants for CdSe QDs and the CdSe/GO nanocomposite are0.0190min–1and0.0345min–1,respectively.The enhanced photocatalytic activity of the CdSe/GO nanocomposite can be attributed to the high specific surface area and the reduction of electron‐hole pair recombination because of the introduction of graphene oxide.展开更多
Vertical MoS2nanosheets were controllably patterned onto graphene as nanoflowers through a two-step hydrothermal method. The interconnected network and intimate contact between MoS2nanosheets and graphene by vertical ...Vertical MoS2nanosheets were controllably patterned onto graphene as nanoflowers through a two-step hydrothermal method. The interconnected network and intimate contact between MoS2nanosheets and graphene by vertical channels enabled a high mechanical integrity of electrode and cycling stability. In particular, MoS2/graphene nanoflowers anode delivered an ultrahigh specific capacity of 901.8 mA·h/g after 700 stable cycles at 1000 mA/g and a corresponding capacity retention as 98.9% from the second cycle onwards.展开更多
We report a γ-ray irradiation reduction method to prepare MnO/reduced graphene oxide （rCO） nanocomposite for the anode of lithium ion batteries. γ-Ray irradiation provides a clean way to generate homogeneously dis...We report a γ-ray irradiation reduction method to prepare MnO/reduced graphene oxide （rCO） nanocomposite for the anode of lithium ion batteries. γ-Ray irradiation provides a clean way to generate homogeneously dispersed MnO nanoparticles with finely tuned size on rGO surface without the use of surfactant. The MnO/rGO composite enables a fully charge/discharge in 2 min to gain a reversible specific capacity of 546 （mA-h）/g which is 45 higher than the theoretical value of commercial graphite anode.展开更多
We explore the electronic and transport properties of zigzag graphene nanoribbons （GNRs） with nitrogen-vacancy defects by performing fully self-consistent spin-polarized density functional theory calculations combin...We explore the electronic and transport properties of zigzag graphene nanoribbons （GNRs） with nitrogen-vacancy defects by performing fully self-consistent spin-polarized density functional theory calculations combined with non-equilibrium Green＇s function technique. We observe robust negative di erential resistance （NDR） effect in all examined molecular junctions. Through analyzing the calculated electronic structures and the bias-dependent transmission coefficients, we find that the narrow density of states of electrodes and the bias-dependent effective coupling between the central molecular orbitals and the electrode subbands are responsible for the observed NDR phenomenon. In addition, the obvious di erence of the transmission spectra of two spin channels is observed in some bias ranges, which leads to the near perfect spin-filtering effect. These theoretical findings imply that GNRs with nitrogenvacancy defects hold great potential for building molecular devices.展开更多
Nanoscale graphene oxide(NGO)sheets were synthesized and used as carbocatalysts for effectiveoxidation of benzylic alcohols and aromatic aldehydes.For oxidation of alcohols in the presence ofH2O2at80°C,the NGOs(2...Nanoscale graphene oxide(NGO)sheets were synthesized and used as carbocatalysts for effectiveoxidation of benzylic alcohols and aromatic aldehydes.For oxidation of alcohols in the presence ofH2O2at80°C,the NGOs(20%mass fraction)as carbocatalysts showed selectivity toward aldehyde.The rate and yield of this reaction strongly depended on the nature of substituents on the alcohol.For4‐nitrobenzyl alcohol,<10%of it was converted into the corresponding carboxylic acid after24h.By contrast,4‐methoxybenzyl alcohol and diphenylmethanol were completely converted into thecorresponding carboxylic acid and ketone after only9and3h,respectively.The conversion ratesfor oxidation of aromatic aldehydes by NGO carbocatalysts were higher than those for alcohol oxidation.For all the aldehydes,complete conversion to the corresponding carboxylic acids wasachieved using7%(mass fraction)of NGO at70°C within2–3h.Possible mechanisms for NGOcarbocatalyst structure‐dependent oxidation of benzyl alcohols and structure‐independent oxidationof aromatic aldehydes are discussed.展开更多
We report a facile coagglomeration method for preparing graphene (G)/MgCl2‐supported Ti‐based Ziegler‐Natta catalysts. The effects of graphene feed ratio on catalyst morphology and ethylene polymerization behavior ...We report a facile coagglomeration method for preparing graphene (G)/MgCl2‐supported Ti‐based Ziegler‐Natta catalysts. The effects of graphene feed ratio on catalyst morphology and ethylene polymerization behavior were examined. The synthesized catalyst exhibited very high activity for ethylene polymerization. The resultant polyethylene (PE)/G nanocomposites showed a layered morphology, and the graphene fillers were well dispersed in the PE matrix. In addition, the thermal stability and mechanical properties of PE were significantly enhanced with the introduction of a very small amount of G fillers (0.05 wt%). This work provides a facile approach to the production o fhigh‐performance PE.展开更多
Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based...Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based electrocatalysts are mentioned. Second, recent updates on gra- phene-derived electrocatalysts are introduced. In this part, both electrochemical activity and stabil- ity of Pt catalysts can be improved when they are supported by reduced graphene oxide （RGO）. Other noble-metal catalysts including Pd, Au, and Ag showing comparable performance have been investigated. The stability of Pd catalyst is enhanced by RGO or few-layered graphene support. Syn- thetic approaches for Au or Ag catalysts supported on graphene oxide are discussed. In addition, non-noble transition metals in N4-chelate complexes can reduce oxygen electrochemically. Fe and Co are cheap alternative catalysts for ORR. In most cases, the stability and tolerance issues are overcome well, but their overall performances don＇t seem to surpass Pt/C catalyst yet,展开更多
Designing cost-effective and high-performance carbon-based oxygen reduction reaction(ORR)electrocatalysts is crucial in the development of Zn-air batteries(ZABs).In this study,a facile one-pot synthesis approach is en...Designing cost-effective and high-performance carbon-based oxygen reduction reaction(ORR)electrocatalysts is crucial in the development of Zn-air batteries(ZABs).In this study,a facile one-pot synthesis approach is engineered to construct Zn/Co-N-C carbonaceous polyhedrons interconnected with self-catalyzed-grown carbon nanotubes(CNTs)from zeolitic imidazolium frameworks linked with graphene oxide nanosheets.The special N-doped threedimensional(3 D)carbon matrix allows manipulating the exposure of active sites and the synergistic interaction between metal nanoparticles and CNTs.The as-synthesized catalyst features impressive ORR activity in 0.1 mol L^(-1)KOH(E_(1/2)=0.83 V)and 0.5 mol L^(-1)H_(2)SO_(4)(E_(1/2)=0.73 V),satisfactory cycling stability and methanol resistance comparable to those of the benchmark Pt/C catalyst(E_(1/2)=0.80 V in 0.1 mol L^(-1)KOH,E_(1/2)=0.75 V in 0.5 mol L^(-1)H_(2)SO_(4)).Furthermore,the asestablished ZAB demonstrates a competitive peak power density(90 mW cm^(-2))and prominent long-term stability,which are better than those of devices based on the commercial Pt/C catalyst(82 mW cm^(-2)).This work provides promising guidance for fabricating highly effective ORR catalysts with in situ formed CNTs,which can be applied in portable ZABrelated devices.展开更多
Lightweight yet strong paper with high toughness is desirable especially for impact protection. Herein we demonstrated electrically conductive and mechanically robust paper(AP/PB-GP) made of reduced graphene oxide via...Lightweight yet strong paper with high toughness is desirable especially for impact protection. Herein we demonstrated electrically conductive and mechanically robust paper(AP/PB-GP) made of reduced graphene oxide via interfacial crosslinking with 1-aminopyrene(AP) and 1-pyrenebutyrat(PB) small molecules. The AP/PB-GP with thickness of over ten micrometer delivers a record-high toughness(~69.67 ± 15.3 MJ m^(-3) in average), simultaneously with superior strength(close to 1 GPa), allowing an impressive specific penetration energy absorption(~0.17 MJ kg^(-1)) at high impact velocities when used for ballistic impact protection. Detailed interfacial and structural analysis reveals that the reinforcement is synergistically determined by π-π interaction and H-bonding linkage between adjacent graphene lamellae. Especially, the defective pores within the graphene platelets benefit the favorable adsorption of the pyrene-containing molecules, which imperatively maximizes the interfacial binding, facilitating deflecting crack and plastic deformation under loading. Density functional theory simulation suggests that the coupling between the polar functional groups, e.g., –COOH, at the edges of graphene platelets and –NH_(2) and –COOH of AP/PB are critical to the formation of hydrogen bonding network.展开更多
The high surface energy of nanomaterials endows them a metastable nature,which greatly limits their application.However,in some cases,the degradation process derived from the poor stability of nanomaterials offers an ...The high surface energy of nanomaterials endows them a metastable nature,which greatly limits their application.However,in some cases,the degradation process derived from the poor stability of nanomaterials offers an unconventional approach to design and obtain functional nanomaterials.Herein,based on the poor stability of ZnSe-[DETA]0.5 hybrid nanobelts,we developed a new strategy to chemically graphitize and functionalize graphene oxide(GO).When ZnSe[DETA]0.5 hybrid nanobelts encountered a strong acid,they were attacked by H^+cations and could release highly reactive Se^2−anions into the reaction solution.Like other common reductants(such as N2H4·H2O),these Se^2−anions exhibited an excellent ability to restore the structure of GO.The structural restoration of GO was greatly affected by the reaction time,the volume of HCl,and the mass ratio between GO and ZnSe[DETA]0.5 nanobelts.By carefully controlling the reaction process and the post-processing process,we finally obtained several Se-based reduced GO(RGO)nanocomposites(such as ZnSe/Se-RGO,ZnSe-RGO,and Se-RGO)and various selenide/metal-RGO nanocomposites(such as Ag2Se-RGO,Cu2Se-RGO,and Pt-RGO).Although the original structure and composition of ZnSe[DETA]0.5 nanobelts are destroyed,the procedure presents an unconventional way to chemically graphitize and functionalize GO and thus provides a new material synthesis platform for nanocomposites.展开更多
Conventional carbon materials cannot combine high density and high porosity,which are required in many applications,typically for energy storage under a limited space.A novel highly dense yet porous carbon has previou...Conventional carbon materials cannot combine high density and high porosity,which are required in many applications,typically for energy storage under a limited space.A novel highly dense yet porous carbon has previously been produced from a three-dimensional(3D)reduced graphene oxide(r-GO)hydrogel by evaporation-induced drying.Here the mechanism of such a network shrinkage in r-GO hydrogel is specifically illustrated by the use of water and 1,4-dioxane,which have a sole difference in surface tension.As a result,the surface tension of the evaporating solvent determines the capillary forces in the nanochannels,which causes shrinkage of the r-GO network.More promisingly,the selection of a solvent with a known surface tension can precisely tune the microstructure associated with the density and porosity of the resulting porous carbon,rendering the porous carbon materials great potential in practical devices with high volumetric performance.展开更多
文摘A 3D nitrogen⁃doped graphene/multi⁃walled carbon nanotube(CS⁃GO⁃NCNT)crosslinked network mate⁃rial was successfully synthesized utilizing chitosan and melamine as carbon and nitrogen sources,concomitant with the incorporation of multi⁃wall carbon nanotubes and employing freeze drying technology.The material amalgamates the merits of 1D/2D hybrid carbon materials,wherein 1D carbon nanotubes confer robustness and expedited elec⁃tron transport pathways,while 2D graphene sheets facilitate rapid ion migration.Furthermore,the introduction of nitrogen heteroatoms serves to furnish additional active sites for lithium storage.When served as an anode material for lithium⁃ion batteries,the CS⁃GO⁃NCNT electrode delivered a reversible capacity surpassing 500 mAh·g^(-1),mark⁃edly outperforming commercial graphite anodes.Even after 300 cycles at a high current density of 1 A·g^(-1),it remained a reversible capacity of up to 268 mAh·g^(-1).
文摘Graphene oxide(GO)with excellent dispersion ability can assist the dispersion of single-walled carbon nanotube(SWCNT)and promote the formation of uniform and stable GO/SWCNT coating liquid.The highly conductive polyethylene terephthalate/reduced graphene oxide/SWCNT(PET/rGO/SWCNT)electromagnetic shielding composite fabric was successfully prepared by anchoring rGO/SWCNT on PET fabric via dip-coating piror to low-temperature thermal reduction.The results showed that the carboxyl groups and hydroxyl groups formed of hydrophilic-treated PET were conducive to the formation of hydrogen bonds with that of GO,which enhanced the interaction between PET fabric and GO/SWCNT coating;the loading of GO/SWCNT increased with the number of dip-coating,the unit area loading of rGO/SWCNT in the final composite fabric was 2.7 mg/cm^(2) after 10 dip-coating cycles and thermal reduction;the PET/rGO/SWCNT composite fabric had a continuous and dense conductive network,with a conductivity of up to 41.6 S/m and the average electromagnetic interference shielding effectiveness in X-band was 22 dB;the flexible PET/rGO/SWCNT composite fabric was not only easy to process,but also exhibited excellent conductivity and shielding efficiency,showing great potential in the application of electromagnetic shielding fabrics.
基金supported by the National Natural Science Foundation of China(51774259)Engineering Research Center of Nano-Geo Materials of Ministry of Education(NGM2017KF004 and NGM2017KF012)~~
文摘CdSe quantum dots(QDs)hybridized with graphene oxide(GO)are synthesized by a facile chemical precipitation method.The absorption of the CdSe/GO nanocomposite is increased with a significantblue shift with respect to CdSe QDs.The specific surface area of the CdSe/GO nanocomposite is10.4m2/g,which is higher than that of CdSe QDs(5m2/g).The PL intensity of the CdSe/GO nanocomposite is lower than that of the CdSe QDs owing to the inhibition of the recombination of electron‐hole pairs in the composite.In Raman analysis,the two bands of the CdSe/GO nanocomposite are shifted to higher wavenumbers with respect to graphene oxide,which is attributed to electron injection that is induced by CdSe QDs into graphene oxide.Using the Brilliant Green dye,the photocatalytic reduction efficiency of CdSe QDs and the CdSe/GO nanocomposite under sunlight irradiation for90min are approximately81.9%and95.5%,respectively.The calculated photodegradation rate constants for CdSe QDs and the CdSe/GO nanocomposite are0.0190min–1and0.0345min–1,respectively.The enhanced photocatalytic activity of the CdSe/GO nanocomposite can be attributed to the high specific surface area and the reduction of electron‐hole pair recombination because of the introduction of graphene oxide.
基金The financial support of the Natural Science Foundation of Changsha,China(No.kq2202094)National Key R&D Program of China(No.2021YFB3701400)。
文摘Vertical MoS2nanosheets were controllably patterned onto graphene as nanoflowers through a two-step hydrothermal method. The interconnected network and intimate contact between MoS2nanosheets and graphene by vertical channels enabled a high mechanical integrity of electrode and cycling stability. In particular, MoS2/graphene nanoflowers anode delivered an ultrahigh specific capacity of 901.8 mA·h/g after 700 stable cycles at 1000 mA/g and a corresponding capacity retention as 98.9% from the second cycle onwards.
基金This work was supported by the National Natural Science Foundation of China （No.21373197）, the 100 Talents Program of the Chinese Academy of Sciences, USTC Startup and the Fundamental Research Funds for the Central Universities （WK2060140018）.
文摘We report a γ-ray irradiation reduction method to prepare MnO/reduced graphene oxide （rCO） nanocomposite for the anode of lithium ion batteries. γ-Ray irradiation provides a clean way to generate homogeneously dispersed MnO nanoparticles with finely tuned size on rGO surface without the use of surfactant. The MnO/rGO composite enables a fully charge/discharge in 2 min to gain a reversible specific capacity of 546 （mA-h）/g which is 45 higher than the theoretical value of commercial graphite anode.
基金This work was partially supported by the National Natural Science Foundation of China （No.20903003 and No.21273208）, the Anhui Provincial Natural Science Foundation （No.1408085QB26）, the China Postdoctoral Science Foundation （No.2012M511409）, the Supercomputer Center of Chinese Academy of Sciences, and University of Science and Technology of China and Shanghai Supercomputer Centers.
文摘We explore the electronic and transport properties of zigzag graphene nanoribbons （GNRs） with nitrogen-vacancy defects by performing fully self-consistent spin-polarized density functional theory calculations combined with non-equilibrium Green＇s function technique. We observe robust negative di erential resistance （NDR） effect in all examined molecular junctions. Through analyzing the calculated electronic structures and the bias-dependent transmission coefficients, we find that the narrow density of states of electrodes and the bias-dependent effective coupling between the central molecular orbitals and the electrode subbands are responsible for the observed NDR phenomenon. In addition, the obvious di erence of the transmission spectra of two spin channels is observed in some bias ranges, which leads to the near perfect spin-filtering effect. These theoretical findings imply that GNRs with nitrogenvacancy defects hold great potential for building molecular devices.
文摘Nanoscale graphene oxide(NGO)sheets were synthesized and used as carbocatalysts for effectiveoxidation of benzylic alcohols and aromatic aldehydes.For oxidation of alcohols in the presence ofH2O2at80°C,the NGOs(20%mass fraction)as carbocatalysts showed selectivity toward aldehyde.The rate and yield of this reaction strongly depended on the nature of substituents on the alcohol.For4‐nitrobenzyl alcohol,<10%of it was converted into the corresponding carboxylic acid after24h.By contrast,4‐methoxybenzyl alcohol and diphenylmethanol were completely converted into thecorresponding carboxylic acid and ketone after only9and3h,respectively.The conversion ratesfor oxidation of aromatic aldehydes by NGO carbocatalysts were higher than those for alcohol oxidation.For all the aldehydes,complete conversion to the corresponding carboxylic acids wasachieved using7%(mass fraction)of NGO at70°C within2–3h.Possible mechanisms for NGOcarbocatalyst structure‐dependent oxidation of benzyl alcohols and structure‐independent oxidationof aromatic aldehydes are discussed.
基金supported by the National Research Foundation of Korea (NRF-2015R1D1A1A0161012)the National Natural Science Foundation of China (U1462124)~~
文摘We report a facile coagglomeration method for preparing graphene (G)/MgCl2‐supported Ti‐based Ziegler‐Natta catalysts. The effects of graphene feed ratio on catalyst morphology and ethylene polymerization behavior were examined. The synthesized catalyst exhibited very high activity for ethylene polymerization. The resultant polyethylene (PE)/G nanocomposites showed a layered morphology, and the graphene fillers were well dispersed in the PE matrix. In addition, the thermal stability and mechanical properties of PE were significantly enhanced with the introduction of a very small amount of G fillers (0.05 wt%). This work provides a facile approach to the production o fhigh‐performance PE.
文摘Very recent progress on the graphene derivatives supported variable nanocatalysts for oxygen reduction reaction （ORR） in fuel cell is reviewed. First, common electrochemical techniques to characterize graphene-based electrocatalysts are mentioned. Second, recent updates on gra- phene-derived electrocatalysts are introduced. In this part, both electrochemical activity and stabil- ity of Pt catalysts can be improved when they are supported by reduced graphene oxide （RGO）. Other noble-metal catalysts including Pd, Au, and Ag showing comparable performance have been investigated. The stability of Pd catalyst is enhanced by RGO or few-layered graphene support. Syn- thetic approaches for Au or Ag catalysts supported on graphene oxide are discussed. In addition, non-noble transition metals in N4-chelate complexes can reduce oxygen electrochemically. Fe and Co are cheap alternative catalysts for ORR. In most cases, the stability and tolerance issues are overcome well, but their overall performances don＇t seem to surpass Pt/C catalyst yet,
基金supported by the National Natural Science Foundation of China(51872076 and U1804255)the Program for Innovative Research Team of Henan Scientific Committee(CXTD2014033)+1 种基金the Project of Central Plains Science and Technology Innovation Leading Talents of Henan Province(194200510001)the Scientific and Technological Research Project of Henan province(212102210651)。
文摘Designing cost-effective and high-performance carbon-based oxygen reduction reaction(ORR)electrocatalysts is crucial in the development of Zn-air batteries(ZABs).In this study,a facile one-pot synthesis approach is engineered to construct Zn/Co-N-C carbonaceous polyhedrons interconnected with self-catalyzed-grown carbon nanotubes(CNTs)from zeolitic imidazolium frameworks linked with graphene oxide nanosheets.The special N-doped threedimensional(3 D)carbon matrix allows manipulating the exposure of active sites and the synergistic interaction between metal nanoparticles and CNTs.The as-synthesized catalyst features impressive ORR activity in 0.1 mol L^(-1)KOH(E_(1/2)=0.83 V)and 0.5 mol L^(-1)H_(2)SO_(4)(E_(1/2)=0.73 V),satisfactory cycling stability and methanol resistance comparable to those of the benchmark Pt/C catalyst(E_(1/2)=0.80 V in 0.1 mol L^(-1)KOH,E_(1/2)=0.75 V in 0.5 mol L^(-1)H_(2)SO_(4)).Furthermore,the asestablished ZAB demonstrates a competitive peak power density(90 mW cm^(-2))and prominent long-term stability,which are better than those of devices based on the commercial Pt/C catalyst(82 mW cm^(-2)).This work provides promising guidance for fabricating highly effective ORR catalysts with in situ formed CNTs,which can be applied in portable ZABrelated devices.
基金supported by the National Natural Science Foundation of China (51772282,51972299)funding from Hefei Center for Physical Science and Technology。
文摘Lightweight yet strong paper with high toughness is desirable especially for impact protection. Herein we demonstrated electrically conductive and mechanically robust paper(AP/PB-GP) made of reduced graphene oxide via interfacial crosslinking with 1-aminopyrene(AP) and 1-pyrenebutyrat(PB) small molecules. The AP/PB-GP with thickness of over ten micrometer delivers a record-high toughness(~69.67 ± 15.3 MJ m^(-3) in average), simultaneously with superior strength(close to 1 GPa), allowing an impressive specific penetration energy absorption(~0.17 MJ kg^(-1)) at high impact velocities when used for ballistic impact protection. Detailed interfacial and structural analysis reveals that the reinforcement is synergistically determined by π-π interaction and H-bonding linkage between adjacent graphene lamellae. Especially, the defective pores within the graphene platelets benefit the favorable adsorption of the pyrene-containing molecules, which imperatively maximizes the interfacial binding, facilitating deflecting crack and plastic deformation under loading. Density functional theory simulation suggests that the coupling between the polar functional groups, e.g., –COOH, at the edges of graphene platelets and –NH_(2) and –COOH of AP/PB are critical to the formation of hydrogen bonding network.
基金This work was supported by the National Natural Science Foundation of China(21431006,51732011,21761132008 and 21805189)the Foundation for Innovative Research Groups of the National Natural Science Foundation of China(21521001)+3 种基金the Key Research Program of Frontier Sciences,Chinese Academy of Sciences(CAS)(QYZDJ-SSW-SLH036)the National Basic Research Program of China(2014CB931800)and the Excellence and Scientific Research Grant from Hefei Science Center of CAS(2015HSC-UE007).This work was partially carried out at the Center for Micro and Nanoscale Research and Fabrication,USTC.Xu L is grateful for the funding support from China Postdoctoral Science Foundation(2018M630711 and 2019T120540)and the Natural Science Foundation of Guangdong(2018A030310617).
文摘The high surface energy of nanomaterials endows them a metastable nature,which greatly limits their application.However,in some cases,the degradation process derived from the poor stability of nanomaterials offers an unconventional approach to design and obtain functional nanomaterials.Herein,based on the poor stability of ZnSe-[DETA]0.5 hybrid nanobelts,we developed a new strategy to chemically graphitize and functionalize graphene oxide(GO).When ZnSe[DETA]0.5 hybrid nanobelts encountered a strong acid,they were attacked by H^+cations and could release highly reactive Se^2−anions into the reaction solution.Like other common reductants(such as N2H4·H2O),these Se^2−anions exhibited an excellent ability to restore the structure of GO.The structural restoration of GO was greatly affected by the reaction time,the volume of HCl,and the mass ratio between GO and ZnSe[DETA]0.5 nanobelts.By carefully controlling the reaction process and the post-processing process,we finally obtained several Se-based reduced GO(RGO)nanocomposites(such as ZnSe/Se-RGO,ZnSe-RGO,and Se-RGO)and various selenide/metal-RGO nanocomposites(such as Ag2Se-RGO,Cu2Se-RGO,and Pt-RGO).Although the original structure and composition of ZnSe[DETA]0.5 nanobelts are destroyed,the procedure presents an unconventional way to chemically graphitize and functionalize GO and thus provides a new material synthesis platform for nanocomposites.
基金This work was supported by the National Natural Science Fund for the Distinguished Young Scholars,China(51525204)the National Natural Science Foundation of China(51702229 and 51872195)the CAS Key Laboratory of Carbon Materials(KLCM KFJJ1704).
文摘Conventional carbon materials cannot combine high density and high porosity,which are required in many applications,typically for energy storage under a limited space.A novel highly dense yet porous carbon has previously been produced from a three-dimensional(3D)reduced graphene oxide(r-GO)hydrogel by evaporation-induced drying.Here the mechanism of such a network shrinkage in r-GO hydrogel is specifically illustrated by the use of water and 1,4-dioxane,which have a sole difference in surface tension.As a result,the surface tension of the evaporating solvent determines the capillary forces in the nanochannels,which causes shrinkage of the r-GO network.More promisingly,the selection of a solvent with a known surface tension can precisely tune the microstructure associated with the density and porosity of the resulting porous carbon,rendering the porous carbon materials great potential in practical devices with high volumetric performance.
