Wang Menglong, Xu Shuai, Zhou Zhaohui, Dong Chung-Li, Guo Xu, Chen Jeng-Lung, Huang Yu-Cheng, Shen Shaohua, Chen Yubin, Guo Liejin, Burda Clemens
International Research Center for Renewable Energy, State Key Laboratory of Multiphase Flow in Power Engineering, Xi'an Jiaotong University, Shaanxi, 710049, China.
Chemical Engineering and Technology, School of Water and Environment, Key Laboratory of Subsurface Hydrology and Ecological Effects in Arid Region, Ministry of Education, Chang'an University, Xi'an, 710064, China.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202204711. doi: 10.1002/anie.202204711. Epub 2022 May 25.
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 at 70 °C, corresponding to an apparent quantum efficiency of 8.9 % at 420 nm excitation wavelength.
单原子镍催化剂因其丰富的活性位点和成本效益,在光催化水分解方面具有巨大潜力。在此,我们采用反应基团导向策略,在红磷上制备原子分散的镍催化剂。红磷的水热处理导致形成P-H和P-OH基团,它们作为反应官能团生成单原子P-Ni和P-O-Ni催化位点的双重结构。产生的单原子位点具有两种不同功能:P-Ni用于水还原,P-O-Ni用于水氧化。受益于这种特殊的双面神结构,与镍纳米颗粒修饰的红磷相比,镍-红磷在可见光照射下表现出更高的析氢速率。随着反应温度升高,析氢速率进一步提高,在70℃时达到91.51 μmol h,对应于420 nm激发波长下8.9%的表观量子效率。