光催化
催化作用
镍
分解水
黑磷
杰纳斯
磷
化学
材料科学
化学工程
环境化学
环境科学
纳米技术
冶金
光电子学
有机化学
工程类
作者
Menglong Wang,Shuai Xu,Zhaohui Zhou,Chung‐Li Dong,Xu Guo,Jeng‐Lung Chen,Yucheng Huang,Shaohua Shen,Yubin Chen,Liejin Guo,Clemens Burda
出处
期刊:Angewandte Chemie
[Wiley]
日期:2022-05-06
卷期号:61 (29): e202204711-e202204711
被引量:92
标识
DOI:10.1002/anie.202204711
摘要
Abstract Single‐atom nickel catalysts hold great promise for photocatalytic water splitting due to their plentiful active sites and cost‐effectiveness. Herein, we adopt a reactive‐group guided strategy to prepare atomically dispersed nickel catalysts on red phosphorus. The hydrothermal treatment of red phosphorus leads to the formation of P−H and P−OH groups, which behave as the reactive functionalities to generate the dual structure of single‐atom P−Ni and P−O−Ni catalytic sites. The produced single‐atom sites provide two different functions: P−Ni for water reduction and P−O−Ni for water oxidation. Benefitting from this specific Janus structure, Ni‐red phosphorus shows an elevated hydrogen evolution rate compared to Ni nanoparticle‐modified red phosphorus under visible‐light irradiation. The hydrogen evolution rate was additionally enhanced with increased reaction temperature, reaching 91.51 μmol h −1 at 70 °C, corresponding to an apparent quantum efficiency of 8.9 % at 420 nm excitation wavelength.
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