Electrocatalytic CO_(2) reduction reaction(CO_(2)RR)holds great promise in green energy conversion and storage.However,for current CO_(2) electrolyzers that rely on the oxygen evolution reaction,a large portion of the...Electrocatalytic CO_(2) reduction reaction(CO_(2)RR)holds great promise in green energy conversion and storage.However,for current CO_(2) electrolyzers that rely on the oxygen evolution reaction,a large portion of the input energy is"wasted"at the anode due to the high overpotential requirement and the recovery of low-value oxygen.To make efficient use of the electricity during electrolysis,coupling CO_(2)RR with anodic alternatives that have low energy demands and/or profitable returns with high-value products is then promising.Herein,we review the latest advances in paired systems for simultaneous CO_(2) reduction and anode valorization.We start with the cases integrating CO_(2)RR with concurrent alternative oxidation,such as inorganic oxidation using chloride,sulfide,ammonia and urea,and organic oxidation using alcohols,aldehydes and primary amines.The paired systems that couple CO_(2)RR with on-site oxidative upgrading of CO_(2)-reduced chemicals are also introduced.The coupling mechanism,electrochemical performance and economic viability of these co-electrolysis systems are discussed.Thereby,we then point out the mismatch issues between the cathodic and anodic reactions regrading catalyst ability,electrolyte solution and reactant supply that will challenge the applications of these paired electrolysis systems.Opportunities to address these issues are further proposed,providing some guidance for future research.展开更多
Hydrogen generation via artificial photosynthesis paves a promising way to remit the ever-increasing energy crisis and deteriorative environmental issues.Among all the materials utilized for solar hydrogen production,...Hydrogen generation via artificial photosynthesis paves a promising way to remit the ever-increasing energy crisis and deteriorative environmental issues.Among all the materials utilized for solar hydrogen production,perovskite has emerged as a rising star due to its superior optoelectronic properties.This manuscript aims to provide a comprehensive review summarizing the recent inspiring advancements on perovskite-based solar hydrogen production systems,including the particulate photocatalysis,photoelectrochemical cells,and photovoltaic-electrocatalytic cells.We start with a brief introduction of the advantages of perovskites for solar hydrogen production and the basic principles of the three most prominent solar hydrogen production systems.The representative progresses in this field are then detailed with a special emphasis on the strategies to improve the efficiency and the stability of the systems.Finally,challenges and opportunities for the further development of the PVK-based solar hydrogen production systems are presented with perspective given on outlook,performance,cost and stability.展开更多
Providing efficient charge transfer through the interface between the semiconductor and co-catalyst is greatly desired in photoelectrocatalytic (PEC) energy conversion.Herein,we excogitate a novel and facile means,via...Providing efficient charge transfer through the interface between the semiconductor and co-catalyst is greatly desired in photoelectrocatalytic (PEC) energy conversion.Herein,we excogitate a novel and facile means,via electrochemical activation,to successfully load the amorphous CoOOH layer architecture onto the surface of TiO_(2).Intriguingly,the as-obtained 6%CoOOH-TiO_(2)photoelectrode manifests optimal PEC performance with a high photocurrent density of 1.3 mA/cm~2,3.5 times higher than that of pristine TiO_(2).Electrochemical impedance spectroscopy (EIS),Tafel analysis and cyclic voltammetry (CV) methods show that the carrier transfer barrier within the electrode and the transition of Co^(3+)OOH to Co^(4+)OOH have the dominating effects on the PEC performance.Theoretical calculation reveals that the interface between the CoOOH and TiO_(2)improves the homogeneity of effective d-orbital electronic-transfer ability among Co sites.This research sheds light on the water oxidation reaction and the design of more favorable PEC cocatalysts.展开更多
Nickel oxides and(oxy)hydroxides are promising replacements for noble-metal-based catalysts owing to their high activity and good long-term stability for the oxygen evolution reaction(OER). Herein, we developed nanopo...Nickel oxides and(oxy)hydroxides are promising replacements for noble-metal-based catalysts owing to their high activity and good long-term stability for the oxygen evolution reaction(OER). Herein, we developed nanoporous Ni by a method of combined rapid solidification and chemical dealloying. Subsequently,nanoporous Ni O was obtained via heating treatment, the macropore and skeleton sizes of the NiO originated from Ni10Al90 alloy are 100–300 nm and 80–200 nm, respectively. Benefiting from the multi-stage nanoporous structure and high specific surface area, the nanoporous NiO demonstrates an outstanding OER, reaching 20 mA cm-2 at an overpotential of 356 mV in 1 M KOH. The corresponding Tafel slope and apparent activation energy are measured to be 76.73 mV dec-1 and 29.0 kJ mol-1, respectively. Moreover,kinetic analysis indicates that the Ni O catalyst shows pseudocapacitive characteristics, and the improved current is attributed to the high-rate pseudocapacitive behavior that efficiently maintains increased nickel redox cycling to accelerate the reaction rates. After 1000 cycles of voltammetry, the overpotential of the NiO decreases by 22 mV(j = 10 mA cm-2), exhibiting excellent stability and durability.展开更多
Hydrogen evolution from water electrolysis has become an important reaction for the green energy revolution.Traditional precious metals and their compounds are excellent catalysts for producing hydrogen;however,their ...Hydrogen evolution from water electrolysis has become an important reaction for the green energy revolution.Traditional precious metals and their compounds are excellent catalysts for producing hydrogen;however,their high cost limits their large-scale practical application.Therefore,the development of affordable electrocatalysts to replace these precious metals is important.Transition metal phosphides(TMPs)have shown remarkable performance for hydrogen evolution and garnered considerable interest in the field of electrolysis.Based on the detailed introduction of TMPs in previous studies,we have systematically summarized the preparation methods,improvement methods,and development opportunities of TMPs and proposed“stimulatory factors”as a fundamental factor affecting the performance of TMPs herein.As the core of this research,“stimulatory factors”can provide numerous solutions to improve the performance of TMP materials and provide a good starting point for TMP research.展开更多
High nickel content layered cathodes,represented by NCM(LiNi_(x)Co_(y)Mn_(z)O_(2),x+y+z=1),are now widely employed in the market of electric vehicles,owing to their high energy density.With the gradual increase of nic...High nickel content layered cathodes,represented by NCM(LiNi_(x)Co_(y)Mn_(z)O_(2),x+y+z=1),are now widely employed in the market of electric vehicles,owing to their high energy density.With the gradual increase of nickel content and capacity,the issues on cycling life and safety become more serious.In this review,various strategies for improving the performance of high nickel NCM are summarized on the aspects of surface coating,ionic doping,and singlecrystal NCM.The coating strategy was separately described according to the physical property of coating species,including inert material coating,Li^(+)-conductor coating,electronic conductor coating,and mixed conductor coating.These coating species help to suppress the interfacial oxidation of electrolytes by NCM,improving the cycling life and safety.The elemental doping in the crystal lattice of NCM is then presented in the aspects of cation,anion,and mixed-ion doping,which are beneficial to stabilize the layered structure during charge–discharge and so promote the electrochemical performance.In quite recent years,the strategy of single-crystal NCM was demonstrated to be a promising pathway,owing to the dramatically reduced surface area and grain boundary.Finally,the remaining unsolved challenges and future strategies for further development of NCM cathode materials are outlined.展开更多
基金financially supported by the National Natural Science Foundation of China(22002084,22072081)the China Postdoctoral Science Foundation(2020M683420)+1 种基金the Fundamental Research Funds for the Central Universities(GK202103111)the 111 Project(B21005)。
文摘Electrocatalytic CO_(2) reduction reaction(CO_(2)RR)holds great promise in green energy conversion and storage.However,for current CO_(2) electrolyzers that rely on the oxygen evolution reaction,a large portion of the input energy is"wasted"at the anode due to the high overpotential requirement and the recovery of low-value oxygen.To make efficient use of the electricity during electrolysis,coupling CO_(2)RR with anodic alternatives that have low energy demands and/or profitable returns with high-value products is then promising.Herein,we review the latest advances in paired systems for simultaneous CO_(2) reduction and anode valorization.We start with the cases integrating CO_(2)RR with concurrent alternative oxidation,such as inorganic oxidation using chloride,sulfide,ammonia and urea,and organic oxidation using alcohols,aldehydes and primary amines.The paired systems that couple CO_(2)RR with on-site oxidative upgrading of CO_(2)-reduced chemicals are also introduced.The coupling mechanism,electrochemical performance and economic viability of these co-electrolysis systems are discussed.Thereby,we then point out the mismatch issues between the cathodic and anodic reactions regrading catalyst ability,electrolyte solution and reactant supply that will challenge the applications of these paired electrolysis systems.Opportunities to address these issues are further proposed,providing some guidance for future research.
基金National Key Research Program of China(2017YFA0204800)National Natural Science Foundation of China(No.21603136)+1 种基金the National Science Basic Research Plan in Shaanxi Province of China(2017JM2007)the Fundamental Research Funds for the Central Universities(2019TS005)。
文摘Hydrogen generation via artificial photosynthesis paves a promising way to remit the ever-increasing energy crisis and deteriorative environmental issues.Among all the materials utilized for solar hydrogen production,perovskite has emerged as a rising star due to its superior optoelectronic properties.This manuscript aims to provide a comprehensive review summarizing the recent inspiring advancements on perovskite-based solar hydrogen production systems,including the particulate photocatalysis,photoelectrochemical cells,and photovoltaic-electrocatalytic cells.We start with a brief introduction of the advantages of perovskites for solar hydrogen production and the basic principles of the three most prominent solar hydrogen production systems.The representative progresses in this field are then detailed with a special emphasis on the strategies to improve the efficiency and the stability of the systems.Finally,challenges and opportunities for the further development of the PVK-based solar hydrogen production systems are presented with perspective given on outlook,performance,cost and stability.
基金support from the National Key Research Program of China (2017YFA0204800, 2016YFA0202403)the Natural Science Foundation of China (No. 21603136)+3 种基金the Changjiang Scholar and Innovative Research Team (IRT_14R33)the Fundamental Research Funds for the Central Universities (GK202003042)The 111 Project (B14041)the Chinese National 1000-Talent-Plan program are also acknowledged。
文摘Providing efficient charge transfer through the interface between the semiconductor and co-catalyst is greatly desired in photoelectrocatalytic (PEC) energy conversion.Herein,we excogitate a novel and facile means,via electrochemical activation,to successfully load the amorphous CoOOH layer architecture onto the surface of TiO_(2).Intriguingly,the as-obtained 6%CoOOH-TiO_(2)photoelectrode manifests optimal PEC performance with a high photocurrent density of 1.3 mA/cm~2,3.5 times higher than that of pristine TiO_(2).Electrochemical impedance spectroscopy (EIS),Tafel analysis and cyclic voltammetry (CV) methods show that the carrier transfer barrier within the electrode and the transition of Co^(3+)OOH to Co^(4+)OOH have the dominating effects on the PEC performance.Theoretical calculation reveals that the interface between the CoOOH and TiO_(2)improves the homogeneity of effective d-orbital electronic-transfer ability among Co sites.This research sheds light on the water oxidation reaction and the design of more favorable PEC cocatalysts.
基金the funding support from the National Natural Science Foundation of China(No.51661018)the support from National Key Research Program of China(2017YFA0204800,2016YFA0202403)+3 种基金Natural Science Foundation of China(No.21603136)the National Science Basic Research Plan in Shaanxi Province of China(2017JM2007)the Changjiang Scholar and Innovative Research Team(IRT_14R33)The 111 Project(B14041)。
文摘Nickel oxides and(oxy)hydroxides are promising replacements for noble-metal-based catalysts owing to their high activity and good long-term stability for the oxygen evolution reaction(OER). Herein, we developed nanoporous Ni by a method of combined rapid solidification and chemical dealloying. Subsequently,nanoporous Ni O was obtained via heating treatment, the macropore and skeleton sizes of the NiO originated from Ni10Al90 alloy are 100–300 nm and 80–200 nm, respectively. Benefiting from the multi-stage nanoporous structure and high specific surface area, the nanoporous NiO demonstrates an outstanding OER, reaching 20 mA cm-2 at an overpotential of 356 mV in 1 M KOH. The corresponding Tafel slope and apparent activation energy are measured to be 76.73 mV dec-1 and 29.0 kJ mol-1, respectively. Moreover,kinetic analysis indicates that the Ni O catalyst shows pseudocapacitive characteristics, and the improved current is attributed to the high-rate pseudocapacitive behavior that efficiently maintains increased nickel redox cycling to accelerate the reaction rates. After 1000 cycles of voltammetry, the overpotential of the NiO decreases by 22 mV(j = 10 mA cm-2), exhibiting excellent stability and durability.
基金the National Natural Science Foundation of China(Nos.22072081,22002084)the Fundamental Research Funds for the Central Universities(Nos.GK202201003,GK2021103111)。
文摘Hydrogen evolution from water electrolysis has become an important reaction for the green energy revolution.Traditional precious metals and their compounds are excellent catalysts for producing hydrogen;however,their high cost limits their large-scale practical application.Therefore,the development of affordable electrocatalysts to replace these precious metals is important.Transition metal phosphides(TMPs)have shown remarkable performance for hydrogen evolution and garnered considerable interest in the field of electrolysis.Based on the detailed introduction of TMPs in previous studies,we have systematically summarized the preparation methods,improvement methods,and development opportunities of TMPs and proposed“stimulatory factors”as a fundamental factor affecting the performance of TMPs herein.As the core of this research,“stimulatory factors”can provide numerous solutions to improve the performance of TMP materials and provide a good starting point for TMP research.
基金National Natural Science Foundation of China,Grant/Award Numbers:21875016,22179004Natural Science Foundation of Beijing,Grant/Award Number:2212014。
文摘High nickel content layered cathodes,represented by NCM(LiNi_(x)Co_(y)Mn_(z)O_(2),x+y+z=1),are now widely employed in the market of electric vehicles,owing to their high energy density.With the gradual increase of nickel content and capacity,the issues on cycling life and safety become more serious.In this review,various strategies for improving the performance of high nickel NCM are summarized on the aspects of surface coating,ionic doping,and singlecrystal NCM.The coating strategy was separately described according to the physical property of coating species,including inert material coating,Li^(+)-conductor coating,electronic conductor coating,and mixed conductor coating.These coating species help to suppress the interfacial oxidation of electrolytes by NCM,improving the cycling life and safety.The elemental doping in the crystal lattice of NCM is then presented in the aspects of cation,anion,and mixed-ion doping,which are beneficial to stabilize the layered structure during charge–discharge and so promote the electrochemical performance.In quite recent years,the strategy of single-crystal NCM was demonstrated to be a promising pathway,owing to the dramatically reduced surface area and grain boundary.Finally,the remaining unsolved challenges and future strategies for further development of NCM cathode materials are outlined.
