光催化
金属
制氢
材料科学
氢
化学工程
光化学
催化作用
壳体(结构)
纳米技术
化学
复合材料
冶金
工程类
有机化学
作者
Duoduo Gao,Wenjing Liu,Ying Xu,Ping Wang,Jiajie Fan,Huogen Yu
标识
DOI:10.1016/j.apcatb.2019.118190
摘要
Abstract Compared with well-known Pt, metallic Ag usually shows a far low H2-evolution rate due to its serious capacitive property and poor H2-evolution activity for Ag-modified photocatalysts. Herein, low-cost metallic Ni cocatalyst is directionally assembled onto the Ag nanoparticle to generate core-shell Ag@Ni cocatalyst, with an aim of greatly boosting the hydrogen-generation performance of metallic Ag. In this case, the core-shell Ag@Ni cocatalyst can be easily loaded onto the TiO2 surface to prepare the core-shell Ag@Ni/TiO2 photocatalysts by a facile one-step photoinduced deposition method. Photocatalytic results manifeste that compared with Ag/TiO2, all the core-shell Ag@Ni/TiO2 samples display a markedly enhanced photocatalytic hydrogen-production rate. Especially, the Ag@Ni/TiO2(1.5:1.5) sample exhibits the highest hydrogen-generation rate (2933.9 μmol h−1 g-1, AQE = 12.12%) due to the synergistic effect of metallic Ag and Ni, namely, Ag core as electronic capturer to efficiently collect photoexcited electrons while Ni shell as interfacial active center to boost hydrogen-generation rate.
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