Aqueous Zn-ion batteries(AZIBs)have been regarded as promising alternatives to Li-ion batteries due to their advantages,such as low cost,high safety,and environmental friendliness.However,AZIBs face significant challe...Aqueous Zn-ion batteries(AZIBs)have been regarded as promising alternatives to Li-ion batteries due to their advantages,such as low cost,high safety,and environmental friendliness.However,AZIBs face significant challenges in limited stability and lifetime owing to zinc dendrite growth and serious side reactions caused by water molecules in the aqueous electrolyte during cycling.To address these issues,a new eutectic electrolyte based on Zn(ClO_(4))_(2)·6H_(2)O-N-methylacetamide(ZN)is proposed in this work.Compared with aqueous electrolyte,the ZN eutectic electrolyte containing organic N-methylacetamide could regulate the solvated structure of Zn^(2+),effectively suppressing zinc dendrite growth and side reactions.As a result,the Zn//NH4 V4 O10 full cell with the eutectic ZN-1-3 electrolyte demonstrates significantly enhanced cycling stability after 1000 cycles at 1 A g^(-1).Therefore,this study not only presents a new eutectic electrolyte for zinc-ion batteries but also provides a deep understanding of the influence of Zn^(2+)solvation structure on the cycle stability,contributing to the exploration of novel electrolytes for high-performance AZIBs.展开更多
The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the ...The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the reduction of greenhouse gas CO_(2)emissions could be achieved.However,the targeted breaking of the C-C/C-H bonds of ethane is still a challenge for the designed catalysts.In this paper,ZnO-doped ZrO_(2)bifunctional catalysts(Zn_(x)ZrO)with different Zn/Zr molar ratios were prepared by the deposition-precipitation method,and the functions of various sites for CO_(2)-ODHE reaction were revealed by in situ characterizations and ethane pulse experiment:the medium-strength acidic Zn-O-Zr sites are responsible for the purposefully cracking of ethane C-H bonds to ethylene,while the more oxygen vacancies(OV)created by the introduction of Zn^(2+)are responsible for the efficient activation C=O bonds of CO_(2),thus promoting the RWGS reaction.In addition,the Zn0.2ZrO catalyst demonstrated excellent catalytic performances,with C_(2)H_(6)conversion,C_(2)H_(4)yield,and CO_(2)conversion about 19.1%,10.5%,and 10.6%within 5 h,respectively(600℃,GHSV=3000 mL/(g·h)).Especially,the initial ethylene space-time yield of 355.5μmol/(min·g)was obtained under 6000 mL/(g·h);Finally,the tandem reaction mechanism of ethane dehydrogenation and RWGS was revealed.展开更多
基金supported by the Natural Science Foundation of Henan Province(No.242300420021)the Major Science and Technology Projects of Henan Province(No.221100230200)+4 种基金the Open Fund of State Key Laboratory of Advanced Refractories(No.SKLAR202210)the Key Science and Technology Program of Henan Province(No.232102241020)the Undergraduate Innovation and Entrepreneurship Training Program of Henan Province(No.S202310464012)the Ph.D.Research Startup Foundation of Henan University of Science and Technology(No.400613480015)the Postdoctoral Research Startup Foundation of Henan University of Science and Technology(No.400613554001).
文摘Aqueous Zn-ion batteries(AZIBs)have been regarded as promising alternatives to Li-ion batteries due to their advantages,such as low cost,high safety,and environmental friendliness.However,AZIBs face significant challenges in limited stability and lifetime owing to zinc dendrite growth and serious side reactions caused by water molecules in the aqueous electrolyte during cycling.To address these issues,a new eutectic electrolyte based on Zn(ClO_(4))_(2)·6H_(2)O-N-methylacetamide(ZN)is proposed in this work.Compared with aqueous electrolyte,the ZN eutectic electrolyte containing organic N-methylacetamide could regulate the solvated structure of Zn^(2+),effectively suppressing zinc dendrite growth and side reactions.As a result,the Zn//NH4 V4 O10 full cell with the eutectic ZN-1-3 electrolyte demonstrates significantly enhanced cycling stability after 1000 cycles at 1 A g^(-1).Therefore,this study not only presents a new eutectic electrolyte for zinc-ion batteries but also provides a deep understanding of the influence of Zn^(2+)solvation structure on the cycle stability,contributing to the exploration of novel electrolytes for high-performance AZIBs.
文摘The CO_(2)-assisted oxidative dehydrogenation of ethane(CO_(2)-ODHE)provides a promising way to produce ethylene and utilize CO_(2).Simultaneous upgrading of ethane into the high value-added chemical products and the reduction of greenhouse gas CO_(2)emissions could be achieved.However,the targeted breaking of the C-C/C-H bonds of ethane is still a challenge for the designed catalysts.In this paper,ZnO-doped ZrO_(2)bifunctional catalysts(Zn_(x)ZrO)with different Zn/Zr molar ratios were prepared by the deposition-precipitation method,and the functions of various sites for CO_(2)-ODHE reaction were revealed by in situ characterizations and ethane pulse experiment:the medium-strength acidic Zn-O-Zr sites are responsible for the purposefully cracking of ethane C-H bonds to ethylene,while the more oxygen vacancies(OV)created by the introduction of Zn^(2+)are responsible for the efficient activation C=O bonds of CO_(2),thus promoting the RWGS reaction.In addition,the Zn0.2ZrO catalyst demonstrated excellent catalytic performances,with C_(2)H_(6)conversion,C_(2)H_(4)yield,and CO_(2)conversion about 19.1%,10.5%,and 10.6%within 5 h,respectively(600℃,GHSV=3000 mL/(g·h)).Especially,the initial ethylene space-time yield of 355.5μmol/(min·g)was obtained under 6000 mL/(g·h);Finally,the tandem reaction mechanism of ethane dehydrogenation and RWGS was revealed.