过电位
材料科学
贵金属
纳米颗粒
石墨烯
金属
氢
基质(水族馆)
纳米技术
分解水
无机化学
化学工程
催化作用
冶金
物理化学
电化学
电极
化学
光催化
有机化学
工程类
海洋学
地质学
作者
Qiqi Li,Zhuo Deng,Dingfeng Tao,Jinyue Pan,Wenli Xu,Zhixuan Zhang,Hongwei Zhong,Yinhong Gao,Qing Shang,Y. Shen J.F. Yu Y.L. Ni,Xuanke Li,Yongting Chen,Qin Zhang
标识
DOI:10.1002/adfm.202411283
摘要
Abstract The catalytic activity of metal nanoparticles is closely pertinent to the substrate, while the influence of the support on the catalytic activity is acquainted scarcely. Herein, the edge selective decoration of noble metal nanoparticles into an edge‐rich carbon foam (CF) matrix for efficient pH‐universal hydrogen evolution (HER) reaction is reported. The highly localized density of states of the graphene edges enables increased reactivity to noble metal nanoparticles and tunes their electronic states. As expected, the Pt nanoparticles decorated on CF (Pt NPs@CF) exhibit low overpotentials ( η 10 ) of only 35, 49, and 53 mV under acidic, alkaline, and neutral conditions, respectively. Moreover, it can deliver the ampere‐level current density of 1000 mA cm −2 with an overpotential of 97 mV in acidic solutions. Above all, the other noble metal NPs decorated on CF also possess efficient pH‐universal HER performance. This work presents a new avenue for developing high‐activity electrocatalysts via support engineering.
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