过电位
催化作用
铂金
电解水
材料科学
化学工程
电解
电解质
合理设计
分解水
无机化学
氢
制氢
化学
纳米技术
电化学
电极
物理化学
光催化
有机化学
工程类
作者
Zhaoming Kang,Jian Cai,Daixin Ye,Hongbin Zhao,Jia-Yang Luo,Jiujun Zhang
标识
DOI:10.1016/j.cej.2022.137443
摘要
Herein, a nitrogen (N)-doped MXene (N-Ti3C2) with a three-dimensional wrinkled morphology was used as an efficient and stable support material to anchor Pt nanoparticles to form a non-carbon supported catalyst ([email protected]) through the coordination interaction between N and O hosted in N-Ti3C2 and Pt. In acidic electrolyte, the resultant [email protected] catalyst exhibited an excellent electrocatalytic HER performance with a low overpotential of 11 mV at 10 mA cm−2, which was superior to that of commercial Pt/C (40 [email protected] mA cm−2). In a water-electrolysis cell, the hydrogen yields of [email protected] catalyst was also higher than that of the Pt/C catalyst in terms of electric energy consumption. The mechanism of the enhanced catalytic HER activity and stability by [email protected] catalyst was explored by theoretical DFT calculations. This work would pave the way for utilizing the MXene family materials as the robust supports toward the rational design of HER electrocatalysts.
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