塔菲尔方程
过电位
材料科学
剥脱关节
空位缺陷
电化学
电导率
催化作用
化学工程
结晶学
纳米技术
石墨烯
物理化学
电极
有机化学
化学
工程类
作者
Yu-Hao Chang,Chongjun Chen,Ching-Hwa Ho,Chau-Yu Cheng,Henghui Chen,Tsu‐Yi Fu,Y.T. Huang,Shuo-Chun Ke,He‐Yun Du,K.Y. Lee,Liang-Chiun Chao,Li‐Chyong Chen,Kuei‐Hsien Chen,Yun‐Ju Chu,R.S. Chen
出处
期刊:Nano Energy
[Elsevier BV]
日期:2021-02-23
卷期号:84: 105922-105922
被引量:44
标识
DOI:10.1016/j.nanoen.2021.105922
摘要
The spontaneous formation of surface electron accumulation (SEA) was observed in synthesized molybdenum diselenide (MoSe2) layered crystals with two-hexagonal (2 H) structure. An anomalously high electron concentration at the surface up to 1019 cm−3 is several orders of magnitude higher than that (3.6 × 1012 cm−3) of the inner bulk. The SEA is found to be generated easily by mechanical exfoliation and room temperature deselenization. Se-vacancies have been confirmed to be the major source resulting in SEA and n-type conductivity, and also the active sites for electrochemical catalysis in MoSe2. Noted that the SEA conjugated with the Se-vacancy-related surface defects enhances the electrochemical hydrogen evolution reaction (HER) activity substantially. The optimized HER efficiency with an overpotential at 0.17 V and Tafel slope at 60 mV/dec of the basal plane of 2 H-MoSe2 was achieved by the nitrogen plasma treatment, which has outperformed several nanostructures, thin films, and hybrid counterparts. This study reveals the intriguing surface-dominant electronic property and its effect on the HER enhancement of the basal plane, which is crucial for development of a stable, low-cost and highly efficient catalyst using 2 H-MoSe2.
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