Water evaporation-induced electricity generation is a promising technology for renewable energy harvesting.However,the output power of some reported two-dimensional(2D)nanofluidic films is still restricted by the rela...Water evaporation-induced electricity generation is a promising technology for renewable energy harvesting.However,the output power of some reported two-dimensional(2D)nanofluidic films is still restricted by the relatively weak water–solid interactions within the tortuous nanochannels.To further enhance the comprehension and utilization of water–solid interactions,it is of utmost importance to conduct an in-depth investigation and propose a regulatory concept encompassing ion transport.Herein,we propose tortuosity regulation of 2D nanofluidic titanium oxide(Ti_(0.87)O_(2))films to optimize the ion transport within the interlayer nanochannel for enhanced efficiency in water evaporation-induced electricity generation for the first time.The significance of tortuosity in ion transport is elucidated by designing three 2D nanofluidic films with different tortuosity.Tortuosity analysis and in situ Raman measurement demonstrate that low tortuosity can facilitate the formation of efficient pathways for hydrated proton transport and promote water–solid interactions.Consequently,devices fabricated with the optimized 2D nanofluidic films exhibited a significantly enhanced output power density of approximately 204.01μW·cm^(−2),far exceeding those prepared by the high-tortuosity 2D nanofluidic films.This work highlights the significance of the construction of low tortuosity channels for 2D nanofluidic films with excellent performance.展开更多
Since its first discovery in 2017,evaporation-induced electricity has attracted extensive attention and shown significant advantages in green energy conversion.While the streaming potential-related electrokinetic effe...Since its first discovery in 2017,evaporation-induced electricity has attracted extensive attention and shown significant advantages in green energy conversion.While the streaming potential-related electrokinetic effect has been intensively explored and widely recognized as the underlying mechanism,the role of coupling between water molecules and charge carriers in the material remains elusive.Here we show through carefully designed experiments that the streaming potential effect indeed plays a role but can only contribute about half to the total water-evaporation-induced voltage occurring within the partially-wetted region of the carbon black film where the solid-liquid-gas three-phase interface exists.It is also shown that water evaporation from carboxyl and amino-functionalized carbon black films produces opposite voltage signals.Detailed first-principles calculations unveil that the adsorption of water molecules can lead to reversed charge transfer in the carboxyl and amino-functionalized carbon substrates.Finally,an evaporation-driven charge transport mechanism is proposed for the induced electricity mediated by the coupling between water molecules and charge carriers in the material.The results reveal the important role of direct interaction between water molecules and materials,deepening our understanding of the mechanism for evaporation-induced hydrovoltaic effect beyond streaming potential.展开更多
We used multibody dissipative particle dynamics method,by which the attractive and repulsive interactions can be effectively considered,to investigate the evaporation-induced morphology patterns of triblock copolymer ...We used multibody dissipative particle dynamics method,by which the attractive and repulsive interactions can be effectively considered,to investigate the evaporation-induced morphology patterns of triblock copolymer A5B10C5 in thin film.With changing attractive interactions between solvent vapor and triblock copolymer that represent various selective solvents,lamellar morphology,sandwich lamellar morphology,spherical morphology and disorder morphology patterns of the thin films were obtained for both coil-coil-coil and rod-coil-coil chain architectures,respectively.The order parameter and the film thickness were calculated during the process for characterizing the film properties,and it was found that the rigid A-block of the triblock copolymer hinders the formation of an ordered structure.展开更多
Highly photoactive bi-phase nanocrystalline TiO2 photocatalyst was prepared by a solvent evaporation-induced crystallization (SEIC) method, and calcined at different temperatures. The obtained TiO2 photocatalyst was c...Highly photoactive bi-phase nanocrystalline TiO2 photocatalyst was prepared by a solvent evaporation-induced crystallization (SEIC) method, and calcined at different temperatures. The obtained TiO2 photocatalyst was characterized with X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface areas. The photocatalytic activity was evaluated by the photocatalytic oxidation of acetone in air. The results show that solvent evaporation can promote the crystallization and phase transformation of TiO2 at 100°C. When calcination temperatures are below 600°C, the prepared TiO2 powders show bimodal pore size distributions in the mesoporous region. At 700°C, the pore size distributions exhibit monomodal distribution of the inter-aggregated pores due to the collapse of the intra-aggregated pores. At 100°C, the obtained TiO2 photocatalyst by this method shows good photocatalytic activity, and at 400°C, its photocatalytic activity exceeds that of Degussa P25. This may be attributed to the fact that the prepared TiO2 photocatalyst has higher specific surface areas, smaller crystallite size and bimodal pore size distribution.展开更多
In recent years,water evaporation-induced electricity has attracted a great deal of attention as an emerging green and renewable energy harvesting technology.Although abundant materials have been developed to fabricat...In recent years,water evaporation-induced electricity has attracted a great deal of attention as an emerging green and renewable energy harvesting technology.Although abundant materials have been developed to fabricate hydrovoltaic devices,the limitations of high costs,inconvenient storage and transport,low environmental benefits,and unadaptable shape have restricted their wide applications.Here,an electricity generator driven by water evaporation has been engineered based on natural biomass leather with inherent properties of good moisture permeability,excellent wettability,physicochemical stability,flexibility,and biocompatibility.Including numerous nano/microchannels together with rich oxygen-bearing functional groups,the natural leather-based water evaporator,Leather_(Emblic-NPs-SA/CB),could continuously produce electricity even staying outside,achieving a maximum output voltage of∼3 V with six-series connection.Furthermore,the leather-based water evaporator has enormous potential for use as a flexible self-powered electronic floor and seawater demineralizer due to its sensitive pressure sensing ability as well as its excellent photothermal conversion efficiency(96.3%)and thus fast water evaporation rate(2.65 kg m^(−2)h^(−1)).This work offers a new and functional material for the construction of hydrovoltaic devices to harvest the sustained green energy from water evaporation in arbitrary ambient environments,which shows great promise in their widespread applications.展开更多
This study developed a facile approach for in situ synthesis of a Ti3＋ self-doped mesoporous TiO 2photocatalyst by an evaporation-induced self-assembly method using TiC l3,water,and F127 as the titanium precursor,sol...This study developed a facile approach for in situ synthesis of a Ti3＋ self-doped mesoporous TiO 2photocatalyst by an evaporation-induced self-assembly method using TiC l3,water,and F127 as the titanium precursor,solvent,and soft template agent,respectively. The as-prepared samples were investigated by X-ray diffraction,N2 adsorption-desorption measurements,ultraviolet-visible diffuse reflectance spectroscopy,electron paramagnetic resonance,and transmission electron microscopy. The influence of different reaction parameters such as the dosage of F127 and calcination temperature on the photocatalytic performance of the resulting products was evaluated. The optimized product exhibited high photocatalytic activity and stability in the oxidation of nitric oxide in air and photocatalytic degradation of methylene blue. The excellent photocatalytic performance of the Ti3＋ self-doped mesoporous TiO 2 photocatalyst is attributed to the cooperation between the mesoporous structure and self-doped Ti3＋ enhancing light absorption and effectively suppressing the recombination of photogenerated electrons and holes.展开更多
Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(...Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(SISA)followed by sulfonation,respectively.In terms of preparation process,SISA(self-assembly in water and preparation time of 2 days)is greener and simpler than EISA(self-assembly in ethanol and preparation time of 7 days).The prepared LDMCE-SO3H and LDMCS-SO3H exhibit obvious differences in structural characteristics such as pore channel structure,specific surface area,mesopore volume and the density of-SO3H groups.Furthermore,the catalytic performances of LDMCE-SO3H and LDMCS-SO3H were investigated in the hydrolysis of microcrystalline cellulose in water,and the glucose yields of 48.99%and 54.42%were obtained under the corresponding optimal reaction conditions.More importantly,the glucose yields still reached 28.85%and 30.35%after five runs,and restored to 39.02%and 45.98%through catalysts regeneration,respectively,demonstrating that LDMCE-SO3H and LDMCS-SO3H have excellent recyclability and regenerability.展开更多
Mesoporous SiO2-ZrO7 nanocomposite was successfully prepared by using supramolecular tfiblock copolymer as the template through evaporation-induced self-assembly approach. The textural and structural properties were c...Mesoporous SiO2-ZrO7 nanocomposite was successfully prepared by using supramolecular tfiblock copolymer as the template through evaporation-induced self-assembly approach. The textural and structural properties were characterized by X-ray diffraction, nitrogen adsorption analysis, and transmission electron microscope. Comparison between pure mesoporous silica and mesoporous silica-zirconia nanocomposite was also presented in this work. The surface area, pore size, and pore volume decreased as the Zr doping in the mesoporous silica framework. But the obtained nanocomposite maintained the cubic Im3m-type mesoporous structure.展开更多
Ordered mesoporous Cu-Mg-A1 composite oxides were synthesized via the one-pot evaporation-in- duced self-assembly strategy. Using this method, copper was first homogeneously incorporated into the ordered mesoporous sp...Ordered mesoporous Cu-Mg-A1 composite oxides were synthesized via the one-pot evaporation-in- duced self-assembly strategy. Using this method, copper was first homogeneously incorporated into the ordered mesoporous spinel matrix. After H2 reduction treatment, according to X-ray diffraction （XRD） and transmission electron microscopy （TEM） results, copper existed as metallic nanoparticles with the size of 6-10 nm that well decorated the parent mesoporous skeleton. The metallic nanoparticles were then re-oxidized to copper oxide when exposed to air or during CO oxidation reaction at low temperatures. Thus, copper migrated from bulk spinel phase to the surface after the reduction-oxidation treat- ment. Moreover, the copper on the surface was re-incor- porated into the bulk spinel phase by further thermal treatment at much higher temperature in the presence of air. The correlation between the state of copper in the mesoporous composite oxides and the catalytic perfor- mance toward CO oxidation was studied. It was found that copper existed as oxide nanoparticles on the surface of mesoporous Mg-Al skeleton is much more active than that existed as lattice Cu ions in spinel phase.展开更多
基金supported by the National Natural Science Foundation of China(Nos.22179062,52125202,and U2004209)the Natural Science Foundation of Jiangsu Province(No.BK2023010081)Fundamental Research Funds for the Central Universities(No.30922010303).
文摘Water evaporation-induced electricity generation is a promising technology for renewable energy harvesting.However,the output power of some reported two-dimensional(2D)nanofluidic films is still restricted by the relatively weak water–solid interactions within the tortuous nanochannels.To further enhance the comprehension and utilization of water–solid interactions,it is of utmost importance to conduct an in-depth investigation and propose a regulatory concept encompassing ion transport.Herein,we propose tortuosity regulation of 2D nanofluidic titanium oxide(Ti_(0.87)O_(2))films to optimize the ion transport within the interlayer nanochannel for enhanced efficiency in water evaporation-induced electricity generation for the first time.The significance of tortuosity in ion transport is elucidated by designing three 2D nanofluidic films with different tortuosity.Tortuosity analysis and in situ Raman measurement demonstrate that low tortuosity can facilitate the formation of efficient pathways for hydrated proton transport and promote water–solid interactions.Consequently,devices fabricated with the optimized 2D nanofluidic films exhibited a significantly enhanced output power density of approximately 204.01μW·cm^(−2),far exceeding those prepared by the high-tortuosity 2D nanofluidic films.This work highlights the significance of the construction of low tortuosity channels for 2D nanofluidic films with excellent performance.
基金the National and Jiangsu Province NSF(T2293691,BK20212008)of ChinaNational Key Research and Development Program of China(2019YFA0705400)+2 种基金the Research Fund of State Key Laboratory of Mechanics and Control of Mechanical Structures(MCMS-I-0422K01)the Fundamental Research Funds for the Central Universities(NJ2022002)the Fund of Prospective Layout of Scientific Research for NUAA(Nanjing University of Aeronautics and Astronautics).
文摘Since its first discovery in 2017,evaporation-induced electricity has attracted extensive attention and shown significant advantages in green energy conversion.While the streaming potential-related electrokinetic effect has been intensively explored and widely recognized as the underlying mechanism,the role of coupling between water molecules and charge carriers in the material remains elusive.Here we show through carefully designed experiments that the streaming potential effect indeed plays a role but can only contribute about half to the total water-evaporation-induced voltage occurring within the partially-wetted region of the carbon black film where the solid-liquid-gas three-phase interface exists.It is also shown that water evaporation from carboxyl and amino-functionalized carbon black films produces opposite voltage signals.Detailed first-principles calculations unveil that the adsorption of water molecules can lead to reversed charge transfer in the carboxyl and amino-functionalized carbon substrates.Finally,an evaporation-driven charge transport mechanism is proposed for the induced electricity mediated by the coupling between water molecules and charge carriers in the material.The results reveal the important role of direct interaction between water molecules and materials,deepening our understanding of the mechanism for evaporation-induced hydrovoltaic effect beyond streaming potential.
基金Supported by the National Natural Science Foundation of China（Nos.21103064, 21173097, 21073075） and the Basic Re- search Fund of Jilin University, China（Nos.450060481158, 450060491249）.
文摘We used multibody dissipative particle dynamics method,by which the attractive and repulsive interactions can be effectively considered,to investigate the evaporation-induced morphology patterns of triblock copolymer A5B10C5 in thin film.With changing attractive interactions between solvent vapor and triblock copolymer that represent various selective solvents,lamellar morphology,sandwich lamellar morphology,spherical morphology and disorder morphology patterns of the thin films were obtained for both coil-coil-coil and rod-coil-coil chain architectures,respectively.The order parameter and the film thickness were calculated during the process for characterizing the film properties,and it was found that the rigid A-block of the triblock copolymer hinders the formation of an ordered structure.
基金This work was partially supported by theNational Natural Science Foundation of China(Grant Nos.50272049,50072016)the Excellent Young Teachers Program of Ministry of Education and the Project-Sponsored by SRF for ROCS of SEMThis work was also financially supported by a grant from the National Natural Science Foundation of China and Research Grant Council of the Hong Kong Special Administrative Region,China(Grant No.N_CUHK433/00).
文摘Highly photoactive bi-phase nanocrystalline TiO2 photocatalyst was prepared by a solvent evaporation-induced crystallization (SEIC) method, and calcined at different temperatures. The obtained TiO2 photocatalyst was characterized with X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface areas. The photocatalytic activity was evaluated by the photocatalytic oxidation of acetone in air. The results show that solvent evaporation can promote the crystallization and phase transformation of TiO2 at 100°C. When calcination temperatures are below 600°C, the prepared TiO2 powders show bimodal pore size distributions in the mesoporous region. At 700°C, the pore size distributions exhibit monomodal distribution of the inter-aggregated pores due to the collapse of the intra-aggregated pores. At 100°C, the obtained TiO2 photocatalyst by this method shows good photocatalytic activity, and at 400°C, its photocatalytic activity exceeds that of Degussa P25. This may be attributed to the fact that the prepared TiO2 photocatalyst has higher specific surface areas, smaller crystallite size and bimodal pore size distribution.
基金supported by the National Natural Science Foundation of China(22308210)the Scientific Research Program Funded by Shaanxi Provincial Education Department(23JK0350)+3 种基金the Open Foundation of Key Laboratory of Auxiliary Chemistry and Technology for Chemical Industry,Ministry of Education,and Shaanxi Collaborative Innovation Center of Industrial Auxiliary Chemistry and Technology,Shaanxi University of Science and Technology(KFKT2021-12)the Opening Project of Key Laboratory of Leather Chemistry and Engineering(Sichuan University),Ministry of Education(2022)the RIKEN-MOST Project between the Ministry of Science and Technology of the People's Republic of China(MOST)and RIKEN,the China Scholarship Council(202108610127)the Natural Science Foundation of Shaanxi University of Science&Technology(2019BT-44).
文摘In recent years,water evaporation-induced electricity has attracted a great deal of attention as an emerging green and renewable energy harvesting technology.Although abundant materials have been developed to fabricate hydrovoltaic devices,the limitations of high costs,inconvenient storage and transport,low environmental benefits,and unadaptable shape have restricted their wide applications.Here,an electricity generator driven by water evaporation has been engineered based on natural biomass leather with inherent properties of good moisture permeability,excellent wettability,physicochemical stability,flexibility,and biocompatibility.Including numerous nano/microchannels together with rich oxygen-bearing functional groups,the natural leather-based water evaporator,Leather_(Emblic-NPs-SA/CB),could continuously produce electricity even staying outside,achieving a maximum output voltage of∼3 V with six-series connection.Furthermore,the leather-based water evaporator has enormous potential for use as a flexible self-powered electronic floor and seawater demineralizer due to its sensitive pressure sensing ability as well as its excellent photothermal conversion efficiency(96.3%)and thus fast water evaporation rate(2.65 kg m^(−2)h^(−1)).This work offers a new and functional material for the construction of hydrovoltaic devices to harvest the sustained green energy from water evaporation in arbitrary ambient environments,which shows great promise in their widespread applications.
基金supported by the National Natural Science Foundation of China(2147707921207090)+2 种基金the Shanghai Rising Star Program(15QA1403300)the Program for Changjiang Scholars and Innovative Research Team(IRT1269)the Specialized Research Fund for the Doctoral Program of Higher Education(20123127120009)~~
文摘This study developed a facile approach for in situ synthesis of a Ti3＋ self-doped mesoporous TiO 2photocatalyst by an evaporation-induced self-assembly method using TiC l3,water,and F127 as the titanium precursor,solvent,and soft template agent,respectively. The as-prepared samples were investigated by X-ray diffraction,N2 adsorption-desorption measurements,ultraviolet-visible diffuse reflectance spectroscopy,electron paramagnetic resonance,and transmission electron microscopy. The influence of different reaction parameters such as the dosage of F127 and calcination temperature on the photocatalytic performance of the resulting products was evaluated. The optimized product exhibited high photocatalytic activity and stability in the oxidation of nitric oxide in air and photocatalytic degradation of methylene blue. The excellent photocatalytic performance of the Ti3＋ self-doped mesoporous TiO 2 photocatalyst is attributed to the cooperation between the mesoporous structure and self-doped Ti3＋ enhancing light absorption and effectively suppressing the recombination of photogenerated electrons and holes.
基金financial support from the National Natural Science Foundation of China(grant No.21706085)Subsidized Project for Postgraduates’Innovative Fund in Scientific Research of Huaqiao Universitythe Foundation of Key Laboratory of Pulp and Paper Science and Technology of Ministry of Education/Shandong Province of China(grant No.KF201804)。
文摘Two kinds of mesoporous carbon solid acids(LDMCE-SO3H and LDMCS-SO3H)were successfully prepared using masson pine alkali lignin as carbon source by evaporation-induced self-assembly(EISA)and salt-induced selfassembly(SISA)followed by sulfonation,respectively.In terms of preparation process,SISA(self-assembly in water and preparation time of 2 days)is greener and simpler than EISA(self-assembly in ethanol and preparation time of 7 days).The prepared LDMCE-SO3H and LDMCS-SO3H exhibit obvious differences in structural characteristics such as pore channel structure,specific surface area,mesopore volume and the density of-SO3H groups.Furthermore,the catalytic performances of LDMCE-SO3H and LDMCS-SO3H were investigated in the hydrolysis of microcrystalline cellulose in water,and the glucose yields of 48.99%and 54.42%were obtained under the corresponding optimal reaction conditions.More importantly,the glucose yields still reached 28.85%and 30.35%after five runs,and restored to 39.02%and 45.98%through catalysts regeneration,respectively,demonstrating that LDMCE-SO3H and LDMCS-SO3H have excellent recyclability and regenerability.
文摘Mesoporous SiO2-ZrO7 nanocomposite was successfully prepared by using supramolecular tfiblock copolymer as the template through evaporation-induced self-assembly approach. The textural and structural properties were characterized by X-ray diffraction, nitrogen adsorption analysis, and transmission electron microscope. Comparison between pure mesoporous silica and mesoporous silica-zirconia nanocomposite was also presented in this work. The surface area, pore size, and pore volume decreased as the Zr doping in the mesoporous silica framework. But the obtained nanocomposite maintained the cubic Im3m-type mesoporous structure.
基金This work was supported by the Recruitment Program of Global Youth Experts of China, the National Natural Science Foundation of China （21403267, 21450110410）, and Shandong Postdoctoral Innovation Program （201303065）.
文摘Ordered mesoporous Cu-Mg-A1 composite oxides were synthesized via the one-pot evaporation-in- duced self-assembly strategy. Using this method, copper was first homogeneously incorporated into the ordered mesoporous spinel matrix. After H2 reduction treatment, according to X-ray diffraction （XRD） and transmission electron microscopy （TEM） results, copper existed as metallic nanoparticles with the size of 6-10 nm that well decorated the parent mesoporous skeleton. The metallic nanoparticles were then re-oxidized to copper oxide when exposed to air or during CO oxidation reaction at low temperatures. Thus, copper migrated from bulk spinel phase to the surface after the reduction-oxidation treat- ment. Moreover, the copper on the surface was re-incor- porated into the bulk spinel phase by further thermal treatment at much higher temperature in the presence of air. The correlation between the state of copper in the mesoporous composite oxides and the catalytic perfor- mance toward CO oxidation was studied. It was found that copper existed as oxide nanoparticles on the surface of mesoporous Mg-Al skeleton is much more active than that existed as lattice Cu ions in spinel phase.
