Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increa...Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increasing attention as active OER catalysts due to their excellent physical and chemical characters,and massive efforts have been devoted to improving the phosphide and sulfide‐based materials with better activity and stability in recent years.In this review,the recent progress on phosphide and sulfide‐based OER electrocatalysts in terms of chemical properties,synthetic methodologies,catalytic performances evaluation and improvement strategy is reviewed.The most accepted reaction pathways as well as the thermodynamics and electrochemistry of the OER are firstly introduced in brief,followed by a summary of the recent research and optimization strategy of phosphide and sulfide‐based OER electrocatalysts.Finally,some mechanistic studies of the active phase of phosphide and sulfide‐based compounds are discussed to give insight into the nature of active catalytic sites.It is expected to indicate guidance for further improving the performances of phosphide and sulfide‐based OER electrocatalysts.展开更多
Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated for electrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. The catalysts co...Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated for electrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. The catalysts comprising MoS2 and MoSa+NiS exhibited good electrical conductivity and catalytic activity. MoS2 and composite catalysts were found to be more active than Pt, a widely used catalyst for high temperature H2S/O2 fuel cell at 750-850℃. However, MoS2 itself sublimes above 450℃. In contrast, composite catalysts containing both Mo and transition metal (Ni) are shown to be stable and effective in promoting the oxidation of H2S in SOFC up to 850℃. However, electric contact is poor between the platinum current collecting layer and the composite metal sulfide layer, so that the cell performance becomes worse. This problem is overcome by adding conductive Ag powder into the anode layer (forming MoS2+NiS+Ag anode material) to increase anode electrical conductance instead of applying a thin layer of platinum on the top of anode.展开更多
A novel type of metal oxide/activated carbon catalyst was prepared by sol-gel method for the hydrolysis of carbonyl sulfide (COS). The influences of the calcination temperature, additive content (2.5%-10.0% Fe2O3, ...A novel type of metal oxide/activated carbon catalyst was prepared by sol-gel method for the hydrolysis of carbonyl sulfide (COS). The influences of the calcination temperature, additive content (2.5%-10.0% Fe2O3, mass fraction) and the basic density of the activation process were thoroughly investigated. The surface of catalysts was characterized by Boehm titration. The products were characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD) and X-ray photoelectron spectroscopy (XPS). The results show that catalysts with 2.5%-5.0% Fe2O3 after calcining at 500 ℃ have superior activity. The conversion rate of COS increases with increasing the relative density of basic capacity loaded onto activated carbon(AC), and the activity follows the order: KOH〉Na2CO3 〉NaHCO3. Boehm titration data clearly show that the total acidity increases (from 0.06 to 0.48 mmol/g) and the basic groups decrease (from 0.78 to 0.56 mmol/g) after COS hydrolysis and H2S adsorption. The XPS results show that the product of HzS may be absorbed by the interaction with metal compounds and 02 to form sulfate (171.28 eV) and element sulfur (164.44 eV), which lead to catalysts poisoning.展开更多
Recently, the photocatalysts have attracted lots of attention and efforts due to their great potential for environmental remediation application. Toxic ions in water are an increasing environmental pollutant with the ...Recently, the photocatalysts have attracted lots of attention and efforts due to their great potential for environmental remediation application. Toxic ions in water are an increasing environmental pollutant with the fast development. Numerous researches have been made to develop photocatalysts to treat ionic pollutants under the illumination of ultraviolet light and visible light. Here, photocatalytic remediation of toxic ionic pollutants has been reviewed. This review summarized and discussed various photocatalysts including TiO〉 modified TiO2, metal oxides, metalsulfides, and nitrides and their recent progress in removing ionic pollutants such as heavy metal ion. The latest achievements and their future prospects of photocatalytic remediation of ion pollutant have also been reviewed.展开更多
文摘Oxygen evolution reaction(OER),as an important half‐reaction involved in water splitting,has been intensely studied since the last century.Transition metal phosphide and sulfide‐based compounds have attracted increasing attention as active OER catalysts due to their excellent physical and chemical characters,and massive efforts have been devoted to improving the phosphide and sulfide‐based materials with better activity and stability in recent years.In this review,the recent progress on phosphide and sulfide‐based OER electrocatalysts in terms of chemical properties,synthetic methodologies,catalytic performances evaluation and improvement strategy is reviewed.The most accepted reaction pathways as well as the thermodynamics and electrochemistry of the OER are firstly introduced in brief,followed by a summary of the recent research and optimization strategy of phosphide and sulfide‐based OER electrocatalysts.Finally,some mechanistic studies of the active phase of phosphide and sulfide‐based compounds are discussed to give insight into the nature of active catalytic sites.It is expected to indicate guidance for further improving the performances of phosphide and sulfide‐based OER electrocatalysts.
文摘Two anode catalysts with Pt, MoS2 and composite metal sulfides (MoS2+NiS), are investigated for electrochemical oxidation of hydrogen sulfide in solid oxide fuel cell (SOFC) at temperatures 750-850℃. The catalysts comprising MoS2 and MoSa+NiS exhibited good electrical conductivity and catalytic activity. MoS2 and composite catalysts were found to be more active than Pt, a widely used catalyst for high temperature H2S/O2 fuel cell at 750-850℃. However, MoS2 itself sublimes above 450℃. In contrast, composite catalysts containing both Mo and transition metal (Ni) are shown to be stable and effective in promoting the oxidation of H2S in SOFC up to 850℃. However, electric contact is poor between the platinum current collecting layer and the composite metal sulfide layer, so that the cell performance becomes worse. This problem is overcome by adding conductive Ag powder into the anode layer (forming MoS2+NiS+Ag anode material) to increase anode electrical conductance instead of applying a thin layer of platinum on the top of anode.
基金Project(50908110) supported by the National Natural Science Foundation of ChinaProject(2008AA062602) supported by the National High-Tech Research and Development Program of China+1 种基金Project(20090451431) supported by China Postdoctoral Science FoundationProject(2007PY01-10) supported by Young and Middle-aged Academic and Technical Back-up Personnel Program of Yunnan Province,China
文摘A novel type of metal oxide/activated carbon catalyst was prepared by sol-gel method for the hydrolysis of carbonyl sulfide (COS). The influences of the calcination temperature, additive content (2.5%-10.0% Fe2O3, mass fraction) and the basic density of the activation process were thoroughly investigated. The surface of catalysts was characterized by Boehm titration. The products were characterized by scanning electron microscopy (SEM), X-ray diffractometry (XRD) and X-ray photoelectron spectroscopy (XPS). The results show that catalysts with 2.5%-5.0% Fe2O3 after calcining at 500 ℃ have superior activity. The conversion rate of COS increases with increasing the relative density of basic capacity loaded onto activated carbon(AC), and the activity follows the order: KOH〉Na2CO3 〉NaHCO3. Boehm titration data clearly show that the total acidity increases (from 0.06 to 0.48 mmol/g) and the basic groups decrease (from 0.78 to 0.56 mmol/g) after COS hydrolysis and H2S adsorption. The XPS results show that the product of HzS may be absorbed by the interaction with metal compounds and 02 to form sulfate (171.28 eV) and element sulfur (164.44 eV), which lead to catalysts poisoning.
基金supported by Recruitment Program of Global Experts in Chinathe Start-up Funds from Shanghai Jiao Tong University+1 种基金the National Natural Science Foundation of China(51372151,21303103)the Foundation of Shanghai Government(15PJ1404000)
文摘Recently, the photocatalysts have attracted lots of attention and efforts due to their great potential for environmental remediation application. Toxic ions in water are an increasing environmental pollutant with the fast development. Numerous researches have been made to develop photocatalysts to treat ionic pollutants under the illumination of ultraviolet light and visible light. Here, photocatalytic remediation of toxic ionic pollutants has been reviewed. This review summarized and discussed various photocatalysts including TiO〉 modified TiO2, metal oxides, metalsulfides, and nitrides and their recent progress in removing ionic pollutants such as heavy metal ion. The latest achievements and their future prospects of photocatalytic remediation of ion pollutant have also been reviewed.