纳米材料基催化剂
材料科学
过电位
纳米颗粒
制氢
催化作用
金属
化学工程
分解水
纳米技术
电化学
物理化学
电极
冶金
光催化
有机化学
工程类
化学
作者
Qi Wang,Mei Ming,Shuai Niu,Yun Zhang,Guangyin Fan,Jin‐Song Hu
标识
DOI:10.1002/aenm.201801698
摘要
Abstract Green and scalable syntheses of highly dispersed supported metal nanocatalysts (SMNCs) are of significant importance for heterogeneous catalysis in industry. In order to achieve nanosized SMNCs and prevent metal nanoparticles (NPs) from aggregation, the traditional liquid syntheses commonly require organic capping agents and low metal loading, which are unfavorable for practical production of SMNCs. Herein, a green and facile solid‐state approach is reported for a general synthesis of Rh, Ru, and Ir NPs highly dispersed on different carbon supports via a room‐temperature mortar grinding. The synthesis is easy to scale up and no organic solvent is needed. Metal NPs are free of capping agents and in a couple of nanometers with a uniform size distribution. Benefiting from the above features and high intrinsic activity, Rh NP/C shows the superior activity for hydrogen evolution reaction (HER) in terms of an ultralow overpotential of 7 mV at 10 mA cm −2 , outperforming the state‐of‐the‐art HER electrocatalysts. The cell voltage to output a stable current density of 10 mA cm −2 is only 1.53 V for the electrolyzer with Rh NP/C cathode. These results indicate that the present scalable solid‐state synthetic strategy paves a new avenue for mass production of highly efficient SMNCs for diverse applications.
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