石墨氮化碳
氮化碳
材料科学
氮化物
碳纤维
催化作用
光催化
化学工程
制氢
氮气
氢
纳米颗粒
纳米技术
复合数
化学
复合材料
有机化学
工程类
图层(电子)
作者
Heng Yang,Ange Zhang,Jianjun Ding,Rui Hu,Yi Gong,Xiangyang Li,Lin Chen,Peng Chen,Xingyou Tian
出处
期刊:Carbon
[Elsevier]
日期:2024-02-01
卷期号:219: 118841-118841
被引量:12
标识
DOI:10.1016/j.carbon.2024.118841
摘要
Bulk graphitic carbon nitride suffers from the disadvantages of a small specific surface area, high recombination of photogenerated charge carriers, and low surface catalytic activity, which greatly limits its application in catalytic reactions. In this study, amino groups were incorporated into the structure of bulk carbon nitride by solvothermal treatment facilitated by an optimal content of urea. The experimental data suggested that the introduced amino groups modified the morphology and structure of bulk carbon nitride, and improved the charge separation. More importantly, the enriched amino groups promoted the formation of nitrogen-rich carbon nitride, which was conducive to the deposition and reduction of ultrafine Pt nanoparticles. The resulting Pt/g-C3N4 composite exhibited excellent visible-light-driven activity for hydrogen evolution. A high rate of 410.51 μmol h−1 with an apparent quantum efficiency of 17 % was achieved, which is 85.5 times higher than that of bulk carbon nitride. The effective approach developed in this work could provide new insights into the design of bulk carbon nitride with enhanced performance.
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