Solar-driven interfacial water evaporation(SIWE)offers a superb way to leverage concentrated solar heat to minimize energy dissipation during seawater desalination.It also engenders overlapped temperaturesalinity grad...Solar-driven interfacial water evaporation(SIWE)offers a superb way to leverage concentrated solar heat to minimize energy dissipation during seawater desalination.It also engenders overlapped temperaturesalinity gradient(TSG)between water-air interface and adjacent seawater,affording opportunities of harnessing electricity.However,the efficiency of conventional SIWE technologies is limited by significant challenges,including salt passivation to hinder evaporation and difficulties in exploiting overlapped TSG simultaneously.Herein,we report self-sustaining hybrid SIWE for not only sustainable seawater desalination but also efficient electricity generation from TSG.It enables spontaneous circulation of salt flux upon seawater evaporation,inducing a self-cleaning evaporative interface without salt passivation for stable steam generation.Meanwhile,this design enables spatial separation and simultaneous utilization of overlapped TSG to enhance electricity generation.These benefits render a remarkable efficiency of90.8%in solar energy utilization,manifesting in co-generation of solar steam at a fast rate of 2.01 kg m^(-2)-h^(-1)and electricity power of 1.91 W m^(-2)with high voltage.Directly interfacing the hybrid SIWE with seawater electrolyzer constructs a system for water-electricity-hydrogen co-generation without external electricity supply.It produces hydrogen at a rapid rate of 1.29 L h^(-1)m^(-2)and freshwater with 22 times lower Na+concentration than the World Health Organization(WHO)threshold.展开更多
In this review, the new solar water treatment technologies, including solar water desalination in two direct and indirect methods, are comprehensively presented. Recent advances and applications of five major solar de...In this review, the new solar water treatment technologies, including solar water desalination in two direct and indirect methods, are comprehensively presented. Recent advances and applications of five major solar desalination technologies include solar-powered humidification–dehumidification, multi-stage flash desalination, multi-effect desalination, RO, and solar stills. Each technology’s productivity, energy consumption, and water production costs are presented. Also, common methods of solar water disinfection have been reviewed as one of the common and low-cost methods of water treatment, especially in areas with no access to drinking water. However, although desalination technologies have many social, economic, and public health benefits, they are energy-intensive and negatively affect the environment. In addition, the disposal of brine from the desalination processes is one of the most challenging and costly issues. In this regard, the environmental effects of desalination technologies are presented and discussed. Among direct solar water desalination technologies, solar still technology is a low-cost, low-tech, and low-investment method suitable for remote areas, especially in developing countries with low financial support and access to skilled workers. Indirect solar-driven water desalination technologies, including thermal and membrane technologies, are more reliable and technically more mature. Recently, RO technology has received particular attention thanks to its lower energy demand, lower cost, and available solutions to increase membrane durability. Disposal of brines can account for much of the water cost and potentially negatively affect the environment. Therefore, in addition to efforts to improve the efficiency and reduce the cost of solar technologies and water treatment processes, future research studies should consider developing new solutions to this issue.展开更多
Synergy between the intrinsic photon and thermal effects from full-spectrum sunlight for H_(2) production is considered to be central to further improve solar-driven H_(2) production.To that end,the photo-thermocataly...Synergy between the intrinsic photon and thermal effects from full-spectrum sunlight for H_(2) production is considered to be central to further improve solar-driven H_(2) production.To that end,the photo-thermocatalyst that demonstrates both photoelectronic and photothermal conversion capabilities have drawn much attention recently.Here,we propose a novel synergistic full-spectrum photo-thermo-catalysis technique for high-efficient H_(2) production by solar-driven methanol steam reforming(MSR),along with the Pt-Cu Oxphoto-thermo-catalyst featuring Pt-Cu/Cu_(2)O/CuO heterojunctions by Pt-mediated in-situ photoreduction of Cu O.The results show that the H_(2) production performance rises superlinearly with increasing light intensity.The optimal H_(2) production rate of 1.6 mol g^(-1) h^(-1) with the corresponding solar-to-hydrogen conversion efficiency of 7%and the CO selectivity of 5%is achieved under 15×sun full-spectrum irradiance(1×sun=1 k W m^(-2))at 180°C,which is much more efficient than the previously-reported Cu-based thermo-catalysts for MSR normally operating at 250~350°C.These attractive performances result from the optimized reaction kinetics in terms of intensified intermediate adsorption and accelerated carrier transfer by long-wave photothermal effect,and reduced activation barrier by short-wave photoelectronic effect,due to the broadened full-spectrum absorbability of catalyst.This work has brought us into the innovative technology of full-spectrum synergistic photothermo-catalysis,which is envisioned to expand the application fields of high-efficient solar fuel production.展开更多
Herein,we report a facile solution process for preparing multi-walled carbon nanotube(MWCNT)bucky paper for solar-driven interfacial water evaporation.This process involves vacuum filtrating a dispersion of MWCNTs tha...Herein,we report a facile solution process for preparing multi-walled carbon nanotube(MWCNT)bucky paper for solar-driven interfacial water evaporation.This process involves vacuum filtrating a dispersion of MWCNTs that was modified by polyvinyl alcohol(PVA)under c-ray irradiation on a cellulose acetate microporous membrane,followed by borate crosslinking.Fourier transform infrared spectroscopy,Raman spectroscopy,and thermogravimetry confirmed the success of PVA grafting onto MWCNTs and borate crosslinking between modified MWCNT nanoyarns.The as-prepared crosslinked MWCNT bucky papers(BBP membranes)were used as a solar absorber,by placing them on a paper-wrapped floating platform,for interfacial water evaporation under simulated solar irradiation.The BBP membranes showed good water tolerance and mechanical stability,with an evaporation rate of 0.79 kg m^(-2)h^(-1)and an evaporation efficiency of 56%under 1 sun illumination in deionized water.Additionally,the BBP membranes achieved an evaporation rate of 0.76 kg m^(-2)h^(-1)in both NaCl solution(3.5 wt%)and sulfuric acid solution(1 mol L-1),demonstrating their impressive applicability for water reclamation from brine and acidic conditions.An evaporation rate of 0.70 kg m-2 h-1(very close to that from deionized water)was obtained from the solar evaporation of saturated NaCl solution,and the BBP membrane exhibited unexpected stability without the inference of salt accumulation on the membrane surface during long-term continuous solar evaporation.展开更多
Interfacial solar evaporation technology is considered one of the most promising strategies for alleviating the scarcity of freshwater resources.However,solar-driven evaporation technology cannot eliminate the polluta...Interfacial solar evaporation technology is considered one of the most promising strategies for alleviating the scarcity of freshwater resources.However,solar-driven evaporation technology cannot eliminate the pollutants in the residual wastewater.To solve this problem,we have prepared a two-in-one solar-driven evaporation/photocatalysis system by decorating MoS_(2)/covalent organic framework(COF)heterojunctions on wood(MoS_(2)/COF-wood).Thanks to the unique porous structure of wood,it provides a strong guarantee for water transport and vapor release during the evaporation process.The introduction of MoS_(2) and COFs can promote the breaking of hydrogen bonds between water molecules,which leads to a significant decrease in the enthalpy of evaporation,achieving a water evaporation rate as high as 2.17 kg m^(-2)h^(-1)under 1 sun irradiation.Meanwhile,the resulting MoS_(2)/COF-wood exhibits good salt resistance and reusability.In addition,the heterojunctions formed between COFs and MoS_(2) can effectively inhibit charge carrier complexation and improve the photocatalytic degradation ability of pollutants(over 99%).This study highlights the construction strategy of bifunctional wood-based materials for freshwater production and wastewater remediation.展开更多
Solar-driven carbon dioxide(CO_(2))conversion including photocatalytic(PC),photoelectrochemical(PEC),photovoltaic plus electrochemical(PV/EC)systems,offers a renewable and scalable way to produce fuels and high-value ...Solar-driven carbon dioxide(CO_(2))conversion including photocatalytic(PC),photoelectrochemical(PEC),photovoltaic plus electrochemical(PV/EC)systems,offers a renewable and scalable way to produce fuels and high-value chemicals for environment and energy sustainability.This review summarizes the basic fundament and the recent advances in the field of solar-driven CO_(2)conversion.Expanding the visible-light absorption is an important strategy to improve solar energy conversion efficiency.The separation and migration of photogenerated charges carriers to surface sites and the surface catalytic processes also determine the photocatalytic performance.Surface engineering including co-catalyst loading,defect engineering,morphology control,surface modification,surface phase junction,and Z-scheme photocatalytic system construction,have become fundamental strategies to obtain high-efficiency photocatalysts.Similar to photocatalysis,these strategies have been applied to improve the conversion efficiency and Faradaic efficiency of typical PEC systems.In PV/EC systems,the electrode surface structure and morphology,electrolyte effects,and mass transport conditions affect the activity and selectivity of electrochemical CO_(2)reduction.Finally,the challenges and prospects are addressed for the development of solar-driven CO_(2)conversion system with high energy conversion efficiency,high product selectivity and stability.展开更多
Solar-driven water evaporation is a sustainable method to purify seawater.Nevertheless,traditional volumetric water-evaporation systems suffer from the poor sunlight absorption and inefficient light-to-thermal convers...Solar-driven water evaporation is a sustainable method to purify seawater.Nevertheless,traditional volumetric water-evaporation systems suffer from the poor sunlight absorption and inefficient light-to-thermal conversion.Also,their anti-bacterial and antifouling performances are crucial for the practical application.Herein,we introduce reduced graphene oxide(RGO)with broadband absorbance across the entire solar spectrum,and polypyrrole(PPy),an antibacterial polymer with efficient solar absorption and low thermal conductivity,to develop integrated RGO/PPy aerogel as both the solar absorber and evaporator for highly efficient solar-driven steam generation.As a result,the RGO/PPy aerogel shows strong absorption and good photothermal performance,leading to an evaporation rate of 1.44 kg·m^(−2)·h^(−1)and high salt rejection(up to 99.99%)for real seawater,with photothermal conversion efficiency>90%under one sun irradiation.The result is attributed to the localized heat at the air-water interface by the RGO/PPy and its porous nature with functional groups that facilitates the water evaporation.Moreover,the RGO/PPy demonstrates excellent durability and antibacterial efficiency close to 100%for 12 h,crucial characteristics for longterm application.Our well-designed RGO/PPy aerogel with efficient water desalination performance and antibacterial property provides a straightforward approach to improve the solar-driven evaporation performance by multifunctional materials integration,and offers a viable route towards practical seawater desalination.展开更多
Synergistically combining biological whole-cell bacteria with man-made semiconductor materials innovates the way for sustainable solar-driven CO_(2)fixation,showing great promise to break through the bottleneck in tra...Synergistically combining biological whole-cell bacteria with man-made semiconductor materials innovates the way for sustainable solar-driven CO_(2)fixation,showing great promise to break through the bottleneck in traditional chemical photocatalyst systems.However,most of the biohybrids require uneconomical organic nutrients and anaerobic conditions for the successful cultivation of the bacteria to sustain the CO_(2)fixation,which severely limits their economic viability and applicability for practical application.Herein,we present an inorganic-biological hybrid system composed of obligate autotrophic bacteria Thiobacillus thioparus(T.thioparus)and CdS nanoparticles(NPs)biologically precipitated on the bacterial surface,which can achieve efficient CO_(2)fixation based entirely on cost-effective inorganic salts and without the restriction of anaerobic conditions.The optimized interface between CdS NPs and T.thioparus formed by biological precipitation plays an essential role for T.thioparus efficiently receiving photogenerated electrons from CdS NPs and thus changing the autotrophic way from chemoautotroph to photoautotroph.As a result,the CdS-T.thioparus biohybrid realizes the solar-driven CO_(2)fixation to produce multi-carbon glutamate synthase and biomass under visible-light irradiation with CO_(2)as the only carbon source.This work provides significant inspiration for the further exploration of the solar-driven self-replicating biocatalytic system to achieve CO_(2)fixation and conversion.展开更多
Pressing need goes ahead for accessing freshwater in insufficient supply countries and regions,which will become a restrictive factor for human development and production.In recent years,solar-driven water evaporation...Pressing need goes ahead for accessing freshwater in insufficient supply countries and regions,which will become a restrictive factor for human development and production.In recent years,solar-driven water evaporation(SDWE)systems have attracted increasing attention for their specialty in no consume conventional energy,pollution-free,and the high purity of fresh water.In particular,carbon-based photothermal conversion materials are preferred light-absorbing material for SDWE systems because of their wide range of spectrum absorption and high photothermal conversion efficiency based on superconjugate effect.Until now,many carbon-based SDWE systems have been reported,and various structures emerged and were designed to enhance light absorption,optimize heat management,and improve the efficient water transport path.In this review,we attempt to give a comprehensive summary and discussions of structure progress of the carbon-based SDWE systems and their working mechanisms,including carbon nanoparticles systems,single-layer photothermal membrane systems,bi-layer structural photothermal systems,porous carbon-based materials systems,and three dimensional(3D)systems.In these systems,the latest 3D systems can expand the light path by allowing light to be reflected multiple times in the microcavity to increase the light absorption rate,and its large heat exchange area can prompt more water to evaporate,which makes them the promising application foreground.We hope our review can spark the probing of underlying principles and inspiring design strategies of these carbonbased SDWE systems,and further guide device optimizations,eventually promoting in extensive practical applications in the future.展开更多
Oxygen vacancy(VO) plays a vital role in semiconductor photocatalysis. Rutile TiO2 nanomaterials with controllable contents of VO(0–2.18%) are fabricated via an insitu solid-state chemical reduction strategy, wit...Oxygen vacancy(VO) plays a vital role in semiconductor photocatalysis. Rutile TiO2 nanomaterials with controllable contents of VO(0–2.18%) are fabricated via an insitu solid-state chemical reduction strategy, with color from white to black. The bandgap of the resultant rutile TiO2 is reduced from 3.0 to 2.56 e V, indicating the enhanced visible light absorption. The resultant rutile TiO2 with optimal contents of VO(2.07%) exhibits a high solar-driven photocatalytic hydrogen production rate of 734 μmol h-1, which is about four times as high as that of the pristine one(185 μmol h-1). The presence of VOelevates the apparent Fermi level of rutile TiO2 and promotes the efficient electronhole separation obviously, which favor the escape of photogenerated electrons and prolong the life-time(7.6×103 ns) of photogenerated charge carriers, confirmed by scanning Kelvin probe microscopy, surface photovoltage spectroscopy and transient-state fluorescence. VO-mediated efficient photogenerated electron-hole separation strategy may provide new insight for fabricating other high-performance semiconductor oxide photocatalysts.展开更多
Remediation of wastewater containing dye molecules is necessary to alleviate the significant threat that poses to human health and the environment.Current treatment technologies are seriously limited by their low effi...Remediation of wastewater containing dye molecules is necessary to alleviate the significant threat that poses to human health and the environment.Current treatment technologies are seriously limited by their low efficiency for removing small dye molecules or/and inferior regenerability.Herein,we report a bio-inspired,solar-driven,regenerable separation device capable of separating small dye molecules from the wastewater with high efficiency.The device is composed of porous super-hydrophilic ceramic and carbon nanotubes(CNTs).In comparison with previously reported systems,the resultant device not only achieved a highly promising separation efficiency of>99%for dye-containing wastewater,even for small dye molecules(<1.25 nm),but also demonstrated excellent separation stability and strong resistance to acid/alkali.Moreover,the device demonstrated impressive regenerability on simple calcination and re-coating of the CNT layer after it was blocked.This novel separation device shows potential for application in many fields,such as dye separation,wastewater purification and desalination.展开更多
Interfacial solar-driven evaporators have presented great potential for water purification owing to their low energy consumption and high steam generation efficiency. However, their further applications are hindered b...Interfacial solar-driven evaporators have presented great potential for water purification owing to their low energy consumption and high steam generation efficiency. However, their further applications are hindered by the high costs and complicated fabrication processes. Here, a scalable bilayer interfacial evaporator was constructed via an affordable technique, in which carbon black deposited nonwoven fabric(CB@NF) was employed as the upper photothermal layer, as well as PVA/starch hybrid hydrogel for selffloating and water transport. Under simulated one sun irradiation, CB@NF layer displayed excellent photothermal conversion performance, whose temperature could increase 30.4 ℃ within 15 min. Moreover,the introduction of starch into PVA endowed the hybrid hydrogels with considerable water-absorption capability on the premise of ensuring mechanical properties. The resultant CB@NF/PVA/starch composites achieved superior interfacial adhesion performance with interfacial toughness at about 200 J m.Combining with good evaporation performance, salt-rejection property and high purification efficiency on pollutants, this evaporation system would become a promising candidate to alleviate water shortage.展开更多
基金This work was supported by the National Key Research and Development Program of China(2022YFB4101600,2022YFB4101605)the National Natural Science Foundation of China(52372175,51972040)+1 种基金the Innovation and Technology Fund of Dalian(N2023JJ12GX020,2022JJ12GX023)Liaoning Normal University 2022 Outstanding Research Achievements Cultivation Fund(No.22GDL002).The authors also acknowledge the assistance of the DUT Instrumental Analysis Center.
文摘Solar-driven interfacial water evaporation(SIWE)offers a superb way to leverage concentrated solar heat to minimize energy dissipation during seawater desalination.It also engenders overlapped temperaturesalinity gradient(TSG)between water-air interface and adjacent seawater,affording opportunities of harnessing electricity.However,the efficiency of conventional SIWE technologies is limited by significant challenges,including salt passivation to hinder evaporation and difficulties in exploiting overlapped TSG simultaneously.Herein,we report self-sustaining hybrid SIWE for not only sustainable seawater desalination but also efficient electricity generation from TSG.It enables spontaneous circulation of salt flux upon seawater evaporation,inducing a self-cleaning evaporative interface without salt passivation for stable steam generation.Meanwhile,this design enables spatial separation and simultaneous utilization of overlapped TSG to enhance electricity generation.These benefits render a remarkable efficiency of90.8%in solar energy utilization,manifesting in co-generation of solar steam at a fast rate of 2.01 kg m^(-2)-h^(-1)and electricity power of 1.91 W m^(-2)with high voltage.Directly interfacing the hybrid SIWE with seawater electrolyzer constructs a system for water-electricity-hydrogen co-generation without external electricity supply.It produces hydrogen at a rapid rate of 1.29 L h^(-1)m^(-2)and freshwater with 22 times lower Na+concentration than the World Health Organization(WHO)threshold.
文摘In this review, the new solar water treatment technologies, including solar water desalination in two direct and indirect methods, are comprehensively presented. Recent advances and applications of five major solar desalination technologies include solar-powered humidification–dehumidification, multi-stage flash desalination, multi-effect desalination, RO, and solar stills. Each technology’s productivity, energy consumption, and water production costs are presented. Also, common methods of solar water disinfection have been reviewed as one of the common and low-cost methods of water treatment, especially in areas with no access to drinking water. However, although desalination technologies have many social, economic, and public health benefits, they are energy-intensive and negatively affect the environment. In addition, the disposal of brine from the desalination processes is one of the most challenging and costly issues. In this regard, the environmental effects of desalination technologies are presented and discussed. Among direct solar water desalination technologies, solar still technology is a low-cost, low-tech, and low-investment method suitable for remote areas, especially in developing countries with low financial support and access to skilled workers. Indirect solar-driven water desalination technologies, including thermal and membrane technologies, are more reliable and technically more mature. Recently, RO technology has received particular attention thanks to its lower energy demand, lower cost, and available solutions to increase membrane durability. Disposal of brines can account for much of the water cost and potentially negatively affect the environment. Therefore, in addition to efforts to improve the efficiency and reduce the cost of solar technologies and water treatment processes, future research studies should consider developing new solutions to this issue.
基金financially supported by the National Natural Science Foundation of China(52176202)the Foshan Xianhu-Laboratory of the Advanced Energy Science and Technology Guangdong Laboratory(41200101)。
文摘Synergy between the intrinsic photon and thermal effects from full-spectrum sunlight for H_(2) production is considered to be central to further improve solar-driven H_(2) production.To that end,the photo-thermocatalyst that demonstrates both photoelectronic and photothermal conversion capabilities have drawn much attention recently.Here,we propose a novel synergistic full-spectrum photo-thermo-catalysis technique for high-efficient H_(2) production by solar-driven methanol steam reforming(MSR),along with the Pt-Cu Oxphoto-thermo-catalyst featuring Pt-Cu/Cu_(2)O/CuO heterojunctions by Pt-mediated in-situ photoreduction of Cu O.The results show that the H_(2) production performance rises superlinearly with increasing light intensity.The optimal H_(2) production rate of 1.6 mol g^(-1) h^(-1) with the corresponding solar-to-hydrogen conversion efficiency of 7%and the CO selectivity of 5%is achieved under 15×sun full-spectrum irradiance(1×sun=1 k W m^(-2))at 180°C,which is much more efficient than the previously-reported Cu-based thermo-catalysts for MSR normally operating at 250~350°C.These attractive performances result from the optimized reaction kinetics in terms of intensified intermediate adsorption and accelerated carrier transfer by long-wave photothermal effect,and reduced activation barrier by short-wave photoelectronic effect,due to the broadened full-spectrum absorbability of catalyst.This work has brought us into the innovative technology of full-spectrum synergistic photothermo-catalysis,which is envisioned to expand the application fields of high-efficient solar fuel production.
基金the National Natural Science Foundation of China(Grants 11875313 and 12075153).
文摘Herein,we report a facile solution process for preparing multi-walled carbon nanotube(MWCNT)bucky paper for solar-driven interfacial water evaporation.This process involves vacuum filtrating a dispersion of MWCNTs that was modified by polyvinyl alcohol(PVA)under c-ray irradiation on a cellulose acetate microporous membrane,followed by borate crosslinking.Fourier transform infrared spectroscopy,Raman spectroscopy,and thermogravimetry confirmed the success of PVA grafting onto MWCNTs and borate crosslinking between modified MWCNT nanoyarns.The as-prepared crosslinked MWCNT bucky papers(BBP membranes)were used as a solar absorber,by placing them on a paper-wrapped floating platform,for interfacial water evaporation under simulated solar irradiation.The BBP membranes showed good water tolerance and mechanical stability,with an evaporation rate of 0.79 kg m^(-2)h^(-1)and an evaporation efficiency of 56%under 1 sun illumination in deionized water.Additionally,the BBP membranes achieved an evaporation rate of 0.76 kg m^(-2)h^(-1)in both NaCl solution(3.5 wt%)and sulfuric acid solution(1 mol L-1),demonstrating their impressive applicability for water reclamation from brine and acidic conditions.An evaporation rate of 0.70 kg m-2 h-1(very close to that from deionized water)was obtained from the solar evaporation of saturated NaCl solution,and the BBP membrane exhibited unexpected stability without the inference of salt accumulation on the membrane surface during long-term continuous solar evaporation.
基金supported by the National Natural Science Foundation of China(22175094,21971113,22108125)the Independent Innovation of Agricultural Science and Technology in Jiangsu Province(CX(21)3163)+2 种基金the Natural Science Foundation of Jiangsu Province(BK20210627)the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX23_1178)the Natural Science Foundation of the Jiangsu Higher Education Institutions(20KJA150001)。
文摘Interfacial solar evaporation technology is considered one of the most promising strategies for alleviating the scarcity of freshwater resources.However,solar-driven evaporation technology cannot eliminate the pollutants in the residual wastewater.To solve this problem,we have prepared a two-in-one solar-driven evaporation/photocatalysis system by decorating MoS_(2)/covalent organic framework(COF)heterojunctions on wood(MoS_(2)/COF-wood).Thanks to the unique porous structure of wood,it provides a strong guarantee for water transport and vapor release during the evaporation process.The introduction of MoS_(2) and COFs can promote the breaking of hydrogen bonds between water molecules,which leads to a significant decrease in the enthalpy of evaporation,achieving a water evaporation rate as high as 2.17 kg m^(-2)h^(-1)under 1 sun irradiation.Meanwhile,the resulting MoS_(2)/COF-wood exhibits good salt resistance and reusability.In addition,the heterojunctions formed between COFs and MoS_(2) can effectively inhibit charge carrier complexation and improve the photocatalytic degradation ability of pollutants(over 99%).This study highlights the construction strategy of bifunctional wood-based materials for freshwater production and wastewater remediation.
基金supported by the National Natural Science Foundation of Chinathe Pioneer Initiative Action Project of the Chinese Academy of Sciences。
文摘Solar-driven carbon dioxide(CO_(2))conversion including photocatalytic(PC),photoelectrochemical(PEC),photovoltaic plus electrochemical(PV/EC)systems,offers a renewable and scalable way to produce fuels and high-value chemicals for environment and energy sustainability.This review summarizes the basic fundament and the recent advances in the field of solar-driven CO_(2)conversion.Expanding the visible-light absorption is an important strategy to improve solar energy conversion efficiency.The separation and migration of photogenerated charges carriers to surface sites and the surface catalytic processes also determine the photocatalytic performance.Surface engineering including co-catalyst loading,defect engineering,morphology control,surface modification,surface phase junction,and Z-scheme photocatalytic system construction,have become fundamental strategies to obtain high-efficiency photocatalysts.Similar to photocatalysis,these strategies have been applied to improve the conversion efficiency and Faradaic efficiency of typical PEC systems.In PV/EC systems,the electrode surface structure and morphology,electrolyte effects,and mass transport conditions affect the activity and selectivity of electrochemical CO_(2)reduction.Finally,the challenges and prospects are addressed for the development of solar-driven CO_(2)conversion system with high energy conversion efficiency,high product selectivity and stability.
基金supported by the National Key R&D Program of China(Nos.2018YFA0209500 and 2018YFA0306900)the National Natural Science Foundation of China(Nos.21872114 and 21627811).
文摘Solar-driven water evaporation is a sustainable method to purify seawater.Nevertheless,traditional volumetric water-evaporation systems suffer from the poor sunlight absorption and inefficient light-to-thermal conversion.Also,their anti-bacterial and antifouling performances are crucial for the practical application.Herein,we introduce reduced graphene oxide(RGO)with broadband absorbance across the entire solar spectrum,and polypyrrole(PPy),an antibacterial polymer with efficient solar absorption and low thermal conductivity,to develop integrated RGO/PPy aerogel as both the solar absorber and evaporator for highly efficient solar-driven steam generation.As a result,the RGO/PPy aerogel shows strong absorption and good photothermal performance,leading to an evaporation rate of 1.44 kg·m^(−2)·h^(−1)and high salt rejection(up to 99.99%)for real seawater,with photothermal conversion efficiency>90%under one sun irradiation.The result is attributed to the localized heat at the air-water interface by the RGO/PPy and its porous nature with functional groups that facilitates the water evaporation.Moreover,the RGO/PPy demonstrates excellent durability and antibacterial efficiency close to 100%for 12 h,crucial characteristics for longterm application.Our well-designed RGO/PPy aerogel with efficient water desalination performance and antibacterial property provides a straightforward approach to improve the solar-driven evaporation performance by multifunctional materials integration,and offers a viable route towards practical seawater desalination.
基金supported by the National Key R&D Program of China(No.2020YFA0406103)the National Natural Science Foundation of China(Nos.21725102,91961106,and 91963108),DNL Cooperation Fund,CAS(No.DNL201922)Youth Innovation Promotion Association CAS.
文摘Synergistically combining biological whole-cell bacteria with man-made semiconductor materials innovates the way for sustainable solar-driven CO_(2)fixation,showing great promise to break through the bottleneck in traditional chemical photocatalyst systems.However,most of the biohybrids require uneconomical organic nutrients and anaerobic conditions for the successful cultivation of the bacteria to sustain the CO_(2)fixation,which severely limits their economic viability and applicability for practical application.Herein,we present an inorganic-biological hybrid system composed of obligate autotrophic bacteria Thiobacillus thioparus(T.thioparus)and CdS nanoparticles(NPs)biologically precipitated on the bacterial surface,which can achieve efficient CO_(2)fixation based entirely on cost-effective inorganic salts and without the restriction of anaerobic conditions.The optimized interface between CdS NPs and T.thioparus formed by biological precipitation plays an essential role for T.thioparus efficiently receiving photogenerated electrons from CdS NPs and thus changing the autotrophic way from chemoautotroph to photoautotroph.As a result,the CdS-T.thioparus biohybrid realizes the solar-driven CO_(2)fixation to produce multi-carbon glutamate synthase and biomass under visible-light irradiation with CO_(2)as the only carbon source.This work provides significant inspiration for the further exploration of the solar-driven self-replicating biocatalytic system to achieve CO_(2)fixation and conversion.
基金the National Key R&D Program of China(2018YFA0209500)the National Natural Science Foundation of China(21621091 and 21975209)the Fundamental Research Funds for the Central Universities(20720190037)。
文摘Pressing need goes ahead for accessing freshwater in insufficient supply countries and regions,which will become a restrictive factor for human development and production.In recent years,solar-driven water evaporation(SDWE)systems have attracted increasing attention for their specialty in no consume conventional energy,pollution-free,and the high purity of fresh water.In particular,carbon-based photothermal conversion materials are preferred light-absorbing material for SDWE systems because of their wide range of spectrum absorption and high photothermal conversion efficiency based on superconjugate effect.Until now,many carbon-based SDWE systems have been reported,and various structures emerged and were designed to enhance light absorption,optimize heat management,and improve the efficient water transport path.In this review,we attempt to give a comprehensive summary and discussions of structure progress of the carbon-based SDWE systems and their working mechanisms,including carbon nanoparticles systems,single-layer photothermal membrane systems,bi-layer structural photothermal systems,porous carbon-based materials systems,and three dimensional(3D)systems.In these systems,the latest 3D systems can expand the light path by allowing light to be reflected multiple times in the microcavity to increase the light absorption rate,and its large heat exchange area can prompt more water to evaporate,which makes them the promising application foreground.We hope our review can spark the probing of underlying principles and inspiring design strategies of these carbonbased SDWE systems,and further guide device optimizations,eventually promoting in extensive practical applications in the future.
基金supported by the Key Program Projects of the National Natural Science Foundation of China (21631004)the National Natural Science Foundation of China (51672073)
文摘Oxygen vacancy(VO) plays a vital role in semiconductor photocatalysis. Rutile TiO2 nanomaterials with controllable contents of VO(0–2.18%) are fabricated via an insitu solid-state chemical reduction strategy, with color from white to black. The bandgap of the resultant rutile TiO2 is reduced from 3.0 to 2.56 e V, indicating the enhanced visible light absorption. The resultant rutile TiO2 with optimal contents of VO(2.07%) exhibits a high solar-driven photocatalytic hydrogen production rate of 734 μmol h-1, which is about four times as high as that of the pristine one(185 μmol h-1). The presence of VOelevates the apparent Fermi level of rutile TiO2 and promotes the efficient electronhole separation obviously, which favor the escape of photogenerated electrons and prolong the life-time(7.6×103 ns) of photogenerated charge carriers, confirmed by scanning Kelvin probe microscopy, surface photovoltage spectroscopy and transient-state fluorescence. VO-mediated efficient photogenerated electron-hole separation strategy may provide new insight for fabricating other high-performance semiconductor oxide photocatalysts.
基金supported by the National Natural Science Foundation of China(Grant Nos.21875011,51922018,51673010)the National Key Research and Development Program of China(Grant No.2017YFA0206904).
文摘Remediation of wastewater containing dye molecules is necessary to alleviate the significant threat that poses to human health and the environment.Current treatment technologies are seriously limited by their low efficiency for removing small dye molecules or/and inferior regenerability.Herein,we report a bio-inspired,solar-driven,regenerable separation device capable of separating small dye molecules from the wastewater with high efficiency.The device is composed of porous super-hydrophilic ceramic and carbon nanotubes(CNTs).In comparison with previously reported systems,the resultant device not only achieved a highly promising separation efficiency of>99%for dye-containing wastewater,even for small dye molecules(<1.25 nm),but also demonstrated excellent separation stability and strong resistance to acid/alkali.Moreover,the device demonstrated impressive regenerability on simple calcination and re-coating of the CNT layer after it was blocked.This novel separation device shows potential for application in many fields,such as dye separation,wastewater purification and desalination.
基金financially supported by the National Natural Science Foundation of China (No.51733002,51803022 and 52003042)the Fundamental Research Funds for the Central Universities (No.2232021D-05)。
文摘Interfacial solar-driven evaporators have presented great potential for water purification owing to their low energy consumption and high steam generation efficiency. However, their further applications are hindered by the high costs and complicated fabrication processes. Here, a scalable bilayer interfacial evaporator was constructed via an affordable technique, in which carbon black deposited nonwoven fabric(CB@NF) was employed as the upper photothermal layer, as well as PVA/starch hybrid hydrogel for selffloating and water transport. Under simulated one sun irradiation, CB@NF layer displayed excellent photothermal conversion performance, whose temperature could increase 30.4 ℃ within 15 min. Moreover,the introduction of starch into PVA endowed the hybrid hydrogels with considerable water-absorption capability on the premise of ensuring mechanical properties. The resultant CB@NF/PVA/starch composites achieved superior interfacial adhesion performance with interfacial toughness at about 200 J m.Combining with good evaporation performance, salt-rejection property and high purification efficiency on pollutants, this evaporation system would become a promising candidate to alleviate water shortage.