塔菲尔方程
电化学
材料科学
单层
插层(化学)
金属
过渡金属
相(物质)
量子点
纳米技术
电极
无机化学
化学
物理化学
冶金
催化作用
有机化学
生物化学
作者
Wenshu Chen,Jiajun Gu,Qinglei Liu,Ruichun Luo,Lulu Yao,Boya Sun,Wang Zhang,Huilan Su,Bin Chen,Pan Liu,Di Zhang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2017-11-29
卷期号:12 (1): 308-316
被引量:140
标识
DOI:10.1021/acsnano.7b06364
摘要
We prepare group VI transitional metal dichalcogenides (TMDs, or MX2) from the 1T phase with quantum-sized and monolayer features via a quasi-full electrochemical process. The resulting two-dimensional (2D) MX2 (M = W, Mo; X = S, Se) quantum dots (QDs) are ca. 3.0-5.4 nm in size with a high 1T phase fraction of ca. 92%-97%. We attribute this to the high Li content intercalated in the 1T-MX2 lattice (mole ratio of Li:M is over 2:1), which is achieved by an increased lithiation driving force and a reduced electrochemical lithiation rate (0.001 A/g). The high Li content not only promotes the 2H → 1T phase transition but also generates significant inner stress that facilitates lattice breaking for MX2 crystals. Because of their high proportion of metallic 1T phase and sufficient active sites induced by the small lateral size, the 2D 1T-MoS2 QDs show excellent hydrogen evolution reactivity (with a typical η10 of 92 mV, Tafel slope of 44 mV/dec, and J0 of 4.16 × 10-4 A/cm2). This electrochemical route toward 2D QDs might help boost the development of 2D materials in energy-related areas.
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