过电位
材料科学
纳米反应器
电场
催化作用
阳极
极化率
曲率
化学物理
偶极子
纳米材料基催化剂
纳米技术
化学工程
氢
领域(数学)
工作(物理)
碳纳米管
氢燃料
析氧
塔菲尔方程
活化能
动力学
反应速率
作者
Hang Wang,Han Xu,Fei Yang,Yan Qing,Fuxiang Chu,Yiqiang Wu,Sheng Ye,Fuquan Xiong
标识
DOI:10.1002/adma.202515230
摘要
Local electric fields of the electrocatalysts can modulate adsorbate binding energies based on their polarizability and dipole moment, which directly influence the catalytic performance. Nevertheless, implementing the prevailing strategy remains challenging due to the scarcity of active sites and sluggish catalytic kinetics. Herein, a continuous heterogeneous-curvature nanoreactor (HeterC-LCS) is created to enhance local electric fields by optimizing the uniform-nanocurvature with tip effects. The H+ concentration and H2O transmission rate of HeterC-LCS are improved by about 2.1 and 1.7 times that of the homogeneous curvature structure (HomoC-LCS) during the hydrogen evolution reaction (HER) process. Besides, HeterC-LCS demonstrates a rapid kinetics of intermediate transformation and an extremely low energy barrier. Such HeterC-LCS depicts a lowest overpotential of 9.2 mV at 10 mA cm-2, which outperforms all known carbon- and Ru-based electrocatalysts. And the mass activity is approximately 60 times that of commercial Pt/C. This work proposes a novel strategy of uniform-nanocurvature optimized by tip effects toward industrially electrocatalytic HER.
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