光催化
纳米团簇
制氢
材料科学
煅烧
氢
化学工程
催化作用
氮气
基质(水族馆)
氧化剂
光催化分解水
分解水
纳米技术
无机化学
化学
有机化学
海洋学
地质学
工程类
作者
Zehui Zhao,Guangmin Ren,Zisheng Zhang,Xiangchao Meng,Zizhen Li
标识
DOI:10.1016/j.seppur.2023.125393
摘要
Solar-driven photocatalytic water splitting for hydrogen production was an essential way to simultaneously solve the energy crisis and environmental pollution problems. C3N4 was a promising substrate for photocatalytic hydrogen production. Herein, we prepared Pt nanoclusters anchored on C3N4 with nitrogen vacancies (Pt/NV-CN) using a rapid Joule heating method. Compared with the traditional calcination method, the Joule heating method not only shortened the preparation time, but also significantly increased the number of reactive sites and further enhanced the photocatalytic activity. Experiments and theoretical calculations confirmed that there was a rapid charge transfer between the metal (Pt) and the substrate (C3N4), and the dual active sites (i.e. nitrogen vacancies and Pt clusters) could decrease the hydrogen adsorption energy. Therefore, as-prepared Pt/NV-CN exhibited excellent hydrogen production activity with a production rate increased from 0 (for pristine C3N4) to 323.90 μmol/h/g, which was also greatly higher than that of Pt/CN-d-VN obtained by traditional tube furnace (97.08 μmol/h/g). This work provided a new method to fabricate the nitrogen vacancies and load Pt clusters onto C3N4 for highly-efficiently photocatalytic H2 production.
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