离域电子
基面
电子
化学物理
原子物理学
材料科学
氢
电流(流体)
电流密度
化学
纳米技术
凝聚态物理
物理
核物理学
有机化学
量子力学
热力学
作者
Jianqiang Chen,Sirui Huang,Yang Yang,Zexin Li,Shenghong Liu,Zhiwen Zhuo,Ning Lü,Xing Zhou,Youwen Liu,Huiqiao Li,Tianyou Zhai
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-06-18
卷期号:24 (26): 8063-8070
被引量:4
标识
DOI:10.1021/acs.nanolett.4c01772
摘要
The basal plane of transition metal dichalcogenides (TMDCs) is inert for the hydrogen evolution reaction (HER) due to its low-efficiency charge transfer kinetics. We propose a strategy of filling the van der Waals (vdW) layer with delocalized electrons to enable vertical penetration of electrons from the collector to the adsorption intermediate vertically. Guided by density functional theory, we achieve this concept by incorporating Cu atoms into the interlayers of tantalum disulfide (TaS2). The delocalized electrons of d-orbitals of the interlayered Cu can constitute the charge transfer pathways in the vertical direction, thus overcoming the hopping migration through vdW gaps. The vertical conductivity of TaS2 increased by 2 orders of magnitude. The TaS2 basal plane HER activity was extracted with an on-chip microcell. Modified by the delocalized electrons, the current density increased by 20 times, reaching an ultrahigh value of 800 mA cm–2 at −0.4 V without iR compensation.
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