材料科学
光催化
金属
催化作用
电子
Atom(片上系统)
氧化物
电子结构
化学物理
纳米技术
计算化学
化学
冶金
嵌入式系统
计算机科学
物理
量子力学
生物化学
作者
Peng Zhou,Fan Lv,Na Li,Yelong Zhang,Zijie Mu,Yonghua Tang,Jianping Lai,Yuguang Chao,Mingchuan Luo,Lin Fei,Jinhui Zhou,Dong Su,Shaojun Guo
出处
期刊:Nano Energy
[Elsevier]
日期:2018-11-15
卷期号:56: 127-137
被引量:293
标识
DOI:10.1016/j.nanoen.2018.11.033
摘要
Tuning reactive metal-support interaction (RMSI) is a promising approach to optimizing catalytic active sites via the electronic, geometric and compositional effects. In general, the RMSI is conducted on the reducible oxides via a high-temperature reaction (>550 °C). Herein we report a strong RMSI between Pt single atom (PtSA) and non-oxide-based g-C3N4 built by an in-situ photocatalytic reduction method at a sub-zero temperature. The experimental observation confirms that the rich N vacancies in g-C3N4 produce an obvious electron-deficient effect, which greatly enhances the RMSI. This strong RMSI contributes to the highest PtSA coverage density of 0.35 mg m−2 reported to date in carbon-based materials and outstanding H2-evolution activity of 174.5 mmol g−1 h−1 per PtSA relative to those on the electron-rich g-C3N4. The structure simulation reveals that the RMSI can not only stabilize the PtSA on the electron-deficient g-C3N4 via the strong chemical bond between PtSA and the two-coordinated C (C2C) sites caused by the N vacancies, but also promises the PtSA with an optimized electronic and geometric structures for capturing photogenerated electrons and producing H2. This finding opens a new channel for designing and manipulating single atom-loaded photocatalyst via the RMSI at a sub-zero low temperature.
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