过电位
钌
电催化剂
纳米颗粒
制氢
材料科学
分解水
纳米技术
密度泛函理论
化学工程
化学
氢
碳纤维
催化作用
物理化学
计算化学
有机化学
电化学
复合材料
工程类
复合数
光催化
电极
作者
Haoqiang Song,Min Wu,Zhiyong Tang,John S. Tse,Bai Yang,Siyu Lu
标识
DOI:10.1002/anie.202017102
摘要
Abstract Ultrathin two‐dimensional catalysts are attracting attention in the field of electrocatalytic hydrogen evolution. This work describe a composite material design in which CoP nanoparticles doped with Ru single‐atom sites supported on carbon dots (CDs) single‐layer nanosheets formed by splicing CDs (Ru 1 CoP/CDs). Small CD fragments bore abundant functional groups, analogous to pieces of a jigsaw puzzle, and could provide a high density of binding sites to immobilize Ru 1 CoP. The single‐particle‐thick nanosheets formed by splicing CDs acted as supports, which improved the conductivity of the electrocatalyst and the stability of the catalyst during operation. The Ru 1 CoP/CDs formed from doping atomic Ru dispersed on CoP showed very high efficiency for the hydrogen evolution reaction (HER) over a wide pH range. The catalyst prepared under optimized conditions displayed outstanding stability and activity: the overpotential for the HER at a current density of 10 mA cm −2 was as low as 51 and 49 mV under alkaline and acidic conditions, respectively. Density functional theory calculations showed that the substituted Ru single atoms lowered the proton‐coupled electron transfer energy barrier and promoted H−H bond formation, thereby enhancing catalytic performance for the HER. The findings open a new avenue for developing carbon‐based hybridization materials with integrated electrocatalytic performance for water splitting.
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