塔菲尔方程
过电位
催化作用
化学
碲
电负性
异质结
电子转移
氢
碲化物
化学工程
电极
材料科学
纳米技术
无机化学
物理化学
光电子学
电化学
有机化学
工程类
生物化学
作者
W. S. Fu,Nan Li,Minghao Shi,Mianmian Wu,Guifang Sun,Wenjing Shen,Qingfei Li,Jiangquan Ma
出处
期刊:Langmuir
[American Chemical Society]
日期:2023-09-07
卷期号:39 (37): 13189-13196
被引量:1
标识
DOI:10.1021/acs.langmuir.3c01613
摘要
Electrocatalytic hydrogen production has been a promising high-purity hydrogen production technology, attracting a large number of researchers' research interest. Ru has a hydrogen binding capacity similar to Pt, but its price is far lower than Pt, making it a promising alternative to Pt. However, a single Se electronic structure modulation is not sufficient to enable RuSe2 to be used for practical applications on a large scale due to the lack of electrons. Therefore, choosing a suitable way to electronically modulate the Ru atoms in RuSe2 can effectively improve the activity of the catalyst. Cobalt telluride (CoTe) can significantly enhance electrocatalytic performance due to tellurium's low electronegativity and excellent metal properties. In this work, the NC layer possesses excellent electrical conductivity and CoTe acts as an electron donor to optimize the electronic structure locally and trigger electron transfer efficiently. The RuSe2–CoTe/NC electrode requires an overpotential of only 25.4 mV (10 mA cm–2), which is superior to that of RuSe2/NF (65 mV) and CoTe/NC (115 mV). Meanwhile, the Tafel slope of RuSe2–CoTe/NC (67.8 mV dec–1) was better than that of RuSe2/NF (113.6 mV dec–1) and CoTe/NC (209.5 mV dec–1), showing that the build-up of the superior heterojunction makes the RuSe2–CoTe/NC with better hydrogen evolution reaction (HER) reaction kinetics. In addition, after 30 h of long-term stability testing, no significant decrease in catalytic activity was observed, proving the good stability of the RuSe2–CoTe/NC catalyst.
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