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作 者:Cui-Hua An Wei Kang Qi-Bo Deng Ning Hu
机构地区:[1]National Engineering Research Center for Technological Innovation Method and Tool,School of Mechanical Engineering,Hebei University of Technology,Tianjin 300401,China [2]Key Laboratory of Advanced Energy Materials Chemistry(MOE),College of Chemistry,Nankai University,Tianjin 300071,China [3]Institute for New Energy Materials&Low-Carbon Technologies,School of Materials Science and Engineering,Tianjin University of Technology,Tianjin 300384,China [4]State Key Laboratory of Reliability and Intelligence Electrical Equipment,Hebei University of Technology,Tianjin 300130,China
出 处:《Rare Metals》2022年第2期378-384,共7页稀有金属(英文版)
基 金:This work was financially supported by the Chinese National Natural Science Fund(No.U1864208);the National Science and Technology Major Project(No.2017-VII-0011-0106);the Science and Technology Planning Project of Tianjin(No.20ZYJDJC00030);the Key Program of Research and Development of Hebei Province(No.202030507040009);the Fund for Innovative Research Groups of Natural Science Foundation of Hebei Province(No.A2020202002).Dr.Qibo Deng acknowledges support from Yuanguang Scholar Program of Hebei University of Technology.
摘 要:Transition metal dichalcogenides,especially MoS_(2),have been examined as promising catalysts for hydrogen evolution reaction(HER).Meanwhile,MoS_(2)with various nanostructures and exposed more active sites has been broadly explored for boosting the HER performances at wide pH range.Here,a synergistic Pt and Te codoping strategy has been used to enhance the catalytic performance(including reducing the overpotential and promoting the HER reaction kinetics)of ultrathin MoS_(2)nanosheets in alkaline and acid electrolytes,which has delivered better than single Pt doping or single Te doping.
关 键 词:DOPING kinetics SYNERGISTIC
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