Anodic polarization behavior of gold, silver, copper, nickel and iron in potentiostatic condition has been examined in an alkaline aqueous thiourea solution, where gold is hardly dissoluble normally. The addition of N...Anodic polarization behavior of gold, silver, copper, nickel and iron in potentiostatic condition has been examined in an alkaline aqueous thiourea solution, where gold is hardly dissoluble normally. The addition of Na2SO3 into the solution can accelerate anodic dissolution of gold. The factors affecting selective dissolution of gold in the alkaline thiourea solution by electrolysis have been studied, and the optimum condition was obtained. In 0.1 mol/L thiourea solution of pH 12. 5 containing 0. 5 mol/L Na2SO3 and 2. 5% acetone, at the potential of 0. 34 V vs NHE, at the temperature of 323 K, the dissolved mass of gold anode with the exposed area of 1. 0 cm2 reached more than 300 mg·dm-3 within 30 min, and other metals such as silver, copper, nickel and iron could hardly dissolve.展开更多
Copper and cadmium ions were selectively separated from zinc sulphate aqueous solution or zinc ammonia/ammonium sulphate aqueous solution by low current density electrolysis.It was shown that the concentration of cadm...Copper and cadmium ions were selectively separated from zinc sulphate aqueous solution or zinc ammonia/ammonium sulphate aqueous solution by low current density electrolysis.It was shown that the concentration of cadmium ion in zinc sulphate solution decreased from 4.56 g/L to 0.18 g/L in an electrolysis time of 8.5 h,whilst it decreased from 5.16 g/L to lower than 0.005 g/L in zinc ammonia/ammonium sulphate aqueous solution.On the other hand,the deposition rate of copper was so low that it was difficult to separate copper and cadmium ions from the zinc ammonia/ammonium sulphate aqueous solution during electrolysis.But copper ion could be decreased to 0.002 g/L in this solution through solvent extraction by using kerosene diluted LIX984N as extractant.Therefore,it is favorable to recover cadmium ion from the zinc ammonia/ammonium sulphate solution by electrolysis after solvent extraction of copper.展开更多
The preparation of Al(OH)3 by the ion exchange membrane electrolysis followed by the precipitation of sodium aluminate solution with seeds was made. During the process of ion membrane electrolysis, the sodium aluminat...The preparation of Al(OH)3 by the ion exchange membrane electrolysis followed by the precipitation of sodium aluminate solution with seeds was made. During the process of ion membrane electrolysis, the sodium aluminate solution is rapidly acidified and the caustic ratio (aK) is decreased due to oxygen evolution in the anodic region. And the causticity of solution is increased due to hydrogen evolution in the cathode region, producing the high concentration of caustic soda solution. Regulating the acidity of the anodic solution by controlling the electric quantity in the electrolysis and subsequent decomposing the solution, Al(OH)3 could yield with very large rate and high efficiency. The experiments also indicate that the quality of aluminum hydroxide product is greatly affected by the impurity silicon.展开更多
Nanometer Al2O3powder is prepared by sol-gel method.Trans mission electron microscope(TEM),X-ray diffrac-tion(XRD),ther mal analysis,IR and the grain-testing instructure are used to characterize the particle shape and...Nanometer Al2O3powder is prepared by sol-gel method.Trans mission electron microscope(TEM),X-ray diffrac-tion(XRD),ther mal analysis,IR and the grain-testing instructure are used to characterize the particle shape and phase,chemical bonds of hydrous cassiterite andsize distribution after being heated.XRDand TEMshowthat the powder is fibrous γ-Al2O3at800 ℃andsphericalα-Al2O3at1 200℃.The grain-testinginstructure shows that the average particle diameter of γ-Al2O3is36.2nm while that ofα-Al2O3is125.6nm.The IRshows that aluminumstearate is synthesizedin the process of sol-gel.展开更多
Polyoxometalates have been explored as multi-electron active species in both aqueous and non-aqueous redox flow batteries. Although non-aqueous systems in principle offer a wider voltage window for redox flow battery ...Polyoxometalates have been explored as multi-electron active species in both aqueous and non-aqueous redox flow batteries. Although non-aqueous systems in principle offer a wider voltage window for redox flow battery operation, realization of this potential requires a judicious choice of solvent as well as polyoxometalate properties. We demonstrate here the superior performance of N,N-dimethylformamide(DMF)compared to acetonitrile as a solvent for redox flow batteries based on Li3PMo12O40. This compound displays two 1-electron transfers in acetonitrile but can access an extra quasi-reversible 2-electron redox process in DMF. A cell containing 10 mM solution of Li3PMo12O40 in DMF produced a cell voltage of 0.7 V with 2-electron transfers(State of Charge = 60%) and showed a good cyclability. As a means to boost energy density, operation of the redox flow battery at a higher concentration of 0.1 M Li3PMo12O40 produced cells with cell voltage of 0.6 V in acetonitrile and a cell voltage of 1.0 V in DMF;both showed excellent coulombic efficiencies of more than 90% over the course of 30 cycles. Energy density was also increased by employing an asymmetric cell with different polyoxometalates on each side to extend cell voltage.Li6P2W18O62 exhibited 3 quasi-reversible 2-electron transfers in the potential range between-2.05 V and-0.5 V vs. Ag/Ag+. 10 mM Li6P2W18O62/Li3PMo12O40 in DMF produced a cell with cell voltage of 1.3 V involving 4-electron transfers(State of Charge = 50%) with coulombic efficiency of nearly 100% and energy efficiency of nearly 70% throughout the test with more than 20 cycles. These promising results demonstrate proof-of-concept approaches to improving the performance of polyoxometalates in non-aqueous redox flow batteries.展开更多
Ytterbium purification by an electrolysis reduction in sulfuric acid medium was investigated without nitrogen or argon protection, in which Ru-Ir-Ti alloy nets and mercury were used as anode and cathode, respectively....Ytterbium purification by an electrolysis reduction in sulfuric acid medium was investigated without nitrogen or argon protection, in which Ru-Ir-Ti alloy nets and mercury were used as anode and cathode, respectively. How the conditions such as the acidities of cathode and anode solutions, and the concentration of Yb（ Ⅲ ） to affect the circuit and ratio of Yb（ Ⅱ ）/Yb （ Ⅲ ） in electrolysis reduction were studied.展开更多
Ammonia has garnered recognition as a zero-carbon fuel due to its high-density hydrogen storage capacity and its convenience for storage and transportation.To address the challenges associated with the direct usage of...Ammonia has garnered recognition as a zero-carbon fuel due to its high-density hydrogen storage capacity and its convenience for storage and transportation.To address the challenges associated with the direct usage of ammonia,the development of NH_(3)-to-H_(2)conversion technologies has emerged as a promising and effective approach.Herein,we present for the first time that crystallized Sm_(2)O_(3−x)electrodes demonstrate high and stable electrocatalytic activities,including N_(2)evolution rate and Faradaic efficiency,for ammonia electrolysis in a non-aqueous electrolyte.It was observed that Sm^(2+)ions in samarium oxide play an indispensable role in the ammonia electrooxidation reaction on the anodes.Furthermore,the mechanism of ammonia electrooxidation has also been elucidated,laying the foundation for a better understanding of the relationship between local structure and electrochemical properties in order to facilitate research on Pt-free electrocatalysts for the electrolysis of ammonia into H_(2).展开更多
Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordi...Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordinary greenhouse gases(GHGs),leading to various environmental issues.Achieving the green production of ammonia is a great challenge,which has been extensively pursued in the last decade.In this review,the most promising strategy,electrochemical nitrate reduction reaction(e-NO_(3)RR),is comprehensively investigated to give a complete understanding of its development and mechanism and provide guidance for future directions.However,owing to the complex reactions and limited selectivity,a comprehensive understanding of the mechanisms is crucial to further development and commercialization.Moreover,NO_(3)^(-)RR is a promising strategy for simultaneous water treatment and NH_(3)production.A detailed overview of the recent progress in NO_(3)^(-)RR for NH_(3)production with nontransition and transition metal based electrocatalysts is summarized.In addition,critical advanced techniques,future challenges,and prospects are discussed to guide future research on transition metal-based catalysts for commercial NH_(3)synthesis by NO_(3)^(-)reduction.展开更多
Theoretical simulations on complex electrochemical processes have been developed on the basis of the understanding in electrochemistry,which has benefited from quantum mechanics calculations.This article reviews the r...Theoretical simulations on complex electrochemical processes have been developed on the basis of the understanding in electrochemistry,which has benefited from quantum mechanics calculations.This article reviews the recent progress on the theory and applications in electrocatalysis.Two representative reactions,namely water electrolysis and oxygen reduction,are selected to illustrate how the theoretical methods are applied to electrocatalytic reactions.The microscopic nature of these electrochemical reactions under the applied potentials is described and the understanding of the reactions is summarized.The thermodynamics and kinetics of the electrochemical reactions affected by the interplay of the electrochemical potential,the bonding strength and the local surface structure are addressed at the atomic level.展开更多
文摘Anodic polarization behavior of gold, silver, copper, nickel and iron in potentiostatic condition has been examined in an alkaline aqueous thiourea solution, where gold is hardly dissoluble normally. The addition of Na2SO3 into the solution can accelerate anodic dissolution of gold. The factors affecting selective dissolution of gold in the alkaline thiourea solution by electrolysis have been studied, and the optimum condition was obtained. In 0.1 mol/L thiourea solution of pH 12. 5 containing 0. 5 mol/L Na2SO3 and 2. 5% acetone, at the potential of 0. 34 V vs NHE, at the temperature of 323 K, the dissolved mass of gold anode with the exposed area of 1. 0 cm2 reached more than 300 mg·dm-3 within 30 min, and other metals such as silver, copper, nickel and iron could hardly dissolve.
基金Projects(50774014,50734005) supported by the National Natural Science Foundation of ChinaProject(2008AA03Z514) supported by the National High-tech Research and Development Program of China
文摘Copper and cadmium ions were selectively separated from zinc sulphate aqueous solution or zinc ammonia/ammonium sulphate aqueous solution by low current density electrolysis.It was shown that the concentration of cadmium ion in zinc sulphate solution decreased from 4.56 g/L to 0.18 g/L in an electrolysis time of 8.5 h,whilst it decreased from 5.16 g/L to lower than 0.005 g/L in zinc ammonia/ammonium sulphate aqueous solution.On the other hand,the deposition rate of copper was so low that it was difficult to separate copper and cadmium ions from the zinc ammonia/ammonium sulphate aqueous solution during electrolysis.But copper ion could be decreased to 0.002 g/L in this solution through solvent extraction by using kerosene diluted LIX984N as extractant.Therefore,it is favorable to recover cadmium ion from the zinc ammonia/ammonium sulphate solution by electrolysis after solvent extraction of copper.
基金Project(2005CB623702) supported by the National Basic Research Program of China
文摘The preparation of Al(OH)3 by the ion exchange membrane electrolysis followed by the precipitation of sodium aluminate solution with seeds was made. During the process of ion membrane electrolysis, the sodium aluminate solution is rapidly acidified and the caustic ratio (aK) is decreased due to oxygen evolution in the anodic region. And the causticity of solution is increased due to hydrogen evolution in the cathode region, producing the high concentration of caustic soda solution. Regulating the acidity of the anodic solution by controlling the electric quantity in the electrolysis and subsequent decomposing the solution, Al(OH)3 could yield with very large rate and high efficiency. The experiments also indicate that the quality of aluminum hydroxide product is greatly affected by the impurity silicon.
文摘Nanometer Al2O3powder is prepared by sol-gel method.Trans mission electron microscope(TEM),X-ray diffrac-tion(XRD),ther mal analysis,IR and the grain-testing instructure are used to characterize the particle shape and phase,chemical bonds of hydrous cassiterite andsize distribution after being heated.XRDand TEMshowthat the powder is fibrous γ-Al2O3at800 ℃andsphericalα-Al2O3at1 200℃.The grain-testinginstructure shows that the average particle diameter of γ-Al2O3is36.2nm while that ofα-Al2O3is125.6nm.The IRshows that aluminumstearate is synthesizedin the process of sol-gel.
文摘Polyoxometalates have been explored as multi-electron active species in both aqueous and non-aqueous redox flow batteries. Although non-aqueous systems in principle offer a wider voltage window for redox flow battery operation, realization of this potential requires a judicious choice of solvent as well as polyoxometalate properties. We demonstrate here the superior performance of N,N-dimethylformamide(DMF)compared to acetonitrile as a solvent for redox flow batteries based on Li3PMo12O40. This compound displays two 1-electron transfers in acetonitrile but can access an extra quasi-reversible 2-electron redox process in DMF. A cell containing 10 mM solution of Li3PMo12O40 in DMF produced a cell voltage of 0.7 V with 2-electron transfers(State of Charge = 60%) and showed a good cyclability. As a means to boost energy density, operation of the redox flow battery at a higher concentration of 0.1 M Li3PMo12O40 produced cells with cell voltage of 0.6 V in acetonitrile and a cell voltage of 1.0 V in DMF;both showed excellent coulombic efficiencies of more than 90% over the course of 30 cycles. Energy density was also increased by employing an asymmetric cell with different polyoxometalates on each side to extend cell voltage.Li6P2W18O62 exhibited 3 quasi-reversible 2-electron transfers in the potential range between-2.05 V and-0.5 V vs. Ag/Ag+. 10 mM Li6P2W18O62/Li3PMo12O40 in DMF produced a cell with cell voltage of 1.3 V involving 4-electron transfers(State of Charge = 50%) with coulombic efficiency of nearly 100% and energy efficiency of nearly 70% throughout the test with more than 20 cycles. These promising results demonstrate proof-of-concept approaches to improving the performance of polyoxometalates in non-aqueous redox flow batteries.
文摘Ytterbium purification by an electrolysis reduction in sulfuric acid medium was investigated without nitrogen or argon protection, in which Ru-Ir-Ti alloy nets and mercury were used as anode and cathode, respectively. How the conditions such as the acidities of cathode and anode solutions, and the concentration of Yb（ Ⅲ ） to affect the circuit and ratio of Yb（ Ⅱ ）/Yb （ Ⅲ ） in electrolysis reduction were studied.
基金supported by the National Natural Science Foundation of China(No.22076081)China Postdoctoral Science Foundation(No.2022M721704).
文摘Ammonia has garnered recognition as a zero-carbon fuel due to its high-density hydrogen storage capacity and its convenience for storage and transportation.To address the challenges associated with the direct usage of ammonia,the development of NH_(3)-to-H_(2)conversion technologies has emerged as a promising and effective approach.Herein,we present for the first time that crystallized Sm_(2)O_(3−x)electrodes demonstrate high and stable electrocatalytic activities,including N_(2)evolution rate and Faradaic efficiency,for ammonia electrolysis in a non-aqueous electrolyte.It was observed that Sm^(2+)ions in samarium oxide play an indispensable role in the ammonia electrooxidation reaction on the anodes.Furthermore,the mechanism of ammonia electrooxidation has also been elucidated,laying the foundation for a better understanding of the relationship between local structure and electrochemical properties in order to facilitate research on Pt-free electrocatalysts for the electrolysis of ammonia into H_(2).
基金supported by the National Natural Science Foundation of China(Grant Nos.22050410268,22176131)Shenzhen Basic Research General Project(JCYJ20210324095205015,JCYJ20220818095601002)。
文摘Ammonia(NH_(3))is an irreplaceable chemical that has been widely demanded to keep the sustainable development of modern society.However,its industrial production consumes a huge amount of energy and releases extraordinary greenhouse gases(GHGs),leading to various environmental issues.Achieving the green production of ammonia is a great challenge,which has been extensively pursued in the last decade.In this review,the most promising strategy,electrochemical nitrate reduction reaction(e-NO_(3)RR),is comprehensively investigated to give a complete understanding of its development and mechanism and provide guidance for future directions.However,owing to the complex reactions and limited selectivity,a comprehensive understanding of the mechanisms is crucial to further development and commercialization.Moreover,NO_(3)^(-)RR is a promising strategy for simultaneous water treatment and NH_(3)production.A detailed overview of the recent progress in NO_(3)^(-)RR for NH_(3)production with nontransition and transition metal based electrocatalysts is summarized.In addition,critical advanced techniques,future challenges,and prospects are discussed to guide future research on transition metal-based catalysts for commercial NH_(3)synthesis by NO_(3)^(-)reduction.
基金supported by the National Natural Science Foundation of China (Grant Nos 20825311, 20773026, and 20721063)Sci & Tech Comm of Shanghai Municipality (08DZ2270500)Program for Professor of Special Appointment (Eastern Scholar) at Shanghai Institute of Higher Learning
文摘Theoretical simulations on complex electrochemical processes have been developed on the basis of the understanding in electrochemistry,which has benefited from quantum mechanics calculations.This article reviews the recent progress on the theory and applications in electrocatalysis.Two representative reactions,namely water electrolysis and oxygen reduction,are selected to illustrate how the theoretical methods are applied to electrocatalytic reactions.The microscopic nature of these electrochemical reactions under the applied potentials is described and the understanding of the reactions is summarized.The thermodynamics and kinetics of the electrochemical reactions affected by the interplay of the electrochemical potential,the bonding strength and the local surface structure are addressed at the atomic level.
