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作 者:Haoxuan Yu Junan Pan Kang Chen Wang Chao Zechao Zhuang Sizhuo Feng Jianmei Chen Lingbin Xie Longlu Wang Qiang Zhao
机构地区:[1]College of Electronic and Optical Engineering&College of Flexible Electronics(Future Technology),Nanjing University of Posts and Telecommunications,9 Wenyuan Road,Nanjing 210023,China [2]Department of Chemical Engineering,Columbia University,New York,NY 10027,USA [3]Institute of Advanced Materials(IAM)&Institute of Flexible Electronics(Future Technology),Nanjing University of Posts and Telecommunications,9 Wenyuan Road,Nanjing 210023,China
出 处:《Nano Research》2024年第8期6910-6915,共6页纳米研究(英文版)
基 金:supported by Innovation Support Programme(Soft Science Research)Project Achievements of Jiangsu Province(No.BK20231514);the National College Student Innovation and Entrepreneurship Training Program(NO.202310293173K).
摘 要:Precise design and synthesis of sub-nano scale catalysts with controllable electronic and geometric structures are pivotal for enhancing the hydrogen evolution reaction(HER)performance of molybdenum sulfide(MoS_(2))and unraveling its structure−activity relationship.By leveraging transition molybdenum polysulfide clusters as functional units for multi-level ordering,we successfully designed and synthesized MoS_(x)nanowire networks derived from[Mo_(3)S_(13)]^(2−) clusters via evaporationinduced self-assembly,which exhibit enhanced HER activity attributed to a high density of active sites and dynamic evolution behavior under cathodic potentials.MoS_(x) nanowire networks electrode yields a current density of 100 mA·cm^(−2) at 142 mV in 0.5 M H_(2)SO_(4).This work provides an attractive prospect for optimizing catalysts at the sub-nano scale and offers insights into a strategy for designing catalysts in various gas evolution reactions.
关 键 词:MoS_(x) nanowire networks [Mo_(3)S_(13)]^(2−)clusters hydrogen evolution reaction(HER) sub-nano scale
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