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通过化学应变激活三元过渡金属硫族化合物基面用于析氢反应

Activation of Ternary Transition Metal Chalcogenide Basal Planes through Chemical Strain for the Hydrogen Evolution Reaction.

作者信息

Kim Yongshin, Tiwari Anand P, Prakash Om, Lee Hyoyoung

机构信息

Department of Chemistry, Sungkyunkwan University (SKKU), Suwon, 16419, Republic of Korea.

Centre for Integrated Nanostructure Physics (CINAP), Institute for Basic Science (IBS), Suwon, 16419, Republic of Korea.

出版信息

Chempluschem. 2017 May;82(5):785-791. doi: 10.1002/cplu.201700164. Epub 2017 May 22.

DOI:10.1002/cplu.201700164
PMID:31961533
Abstract

Catalytically inactive basal planes pose challenges for the efficient hydrogen evolution reaction (HER) in two-dimensional (2 D) transition metal chalcogenide (TMC) nanosheets. Herein, a new hybrid structure is reported in which zero-dimensional TMC nanodots (NDs) are decorated on the basal planes of 2 D nanosheets of TMCs to enhance their catalytic activity towards the HER process. A novel process is developed to fabricate a hybrid Cu MoS (2 D ternary transition metal chalcogenide Cu MoS nanosheets)/MoSe (0 D binary transition metal chalcogenide MoSe ND) nanostructure by controlling the size of the MoSe NDs to enhance the HER activity. In acidic media, this optimal hybrid Cu MoS /MoSe nanostructure achieves excellent catalytic activity for HER, which exhibits a low overpotential of 166 mV at a current density of 10 mA cm , which corresponds to a Tafel slope of 74.7 mV dec . In addition, the synthesized hybrid nanostructure shows excellent stability when under acidic medium for 16 h of continuous electrolysis. Therefore, it is suggested that our strategy may open a new path for the design of hybrid nanostructures by using ternary transition metal chalcogenides (TTMCs) with binary transition metal chalcogenides (BTMCs) for alternative non-noble metal catalysts towards HER.

摘要

在二维(2D)过渡金属硫族化物(TMC)纳米片中,催化惰性的基面给高效析氢反应(HER)带来了挑战。在此,报道了一种新型杂化结构,其中零维TMC纳米点(NDs)修饰在TMC二维纳米片的基面上,以增强其对HER过程的催化活性。通过控制MoSe NDs的尺寸,开发了一种新颖的方法来制备杂化CuMoS(二维三元过渡金属硫族化物CuMoS纳米片)/MoSe(零维二元过渡金属硫族化物MoSe ND)纳米结构,以增强HER活性。在酸性介质中,这种最佳的杂化CuMoS/MoSe纳米结构对HER具有优异的催化活性,在电流密度为10 mA cm时表现出166 mV的低过电位,对应的塔菲尔斜率为74.7 mV dec。此外,合成的杂化纳米结构在酸性介质中连续电解16小时时表现出优异的稳定性。因此,建议我们的策略可能为通过使用三元过渡金属硫族化物(TTMCs)与二元过渡金属硫族化物(BTMCs)设计杂化纳米结构开辟一条新途径,以用于替代非贵金属HER催化剂。

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