光催化
材料科学
分解水
X射线光电子能谱
氮气
光催化分解水
石墨氮化碳
化学工程
聚合
氮化碳
量子效率
氮化物
碳纤维
表面改性
氢
纳米技术
光化学
光电子学
催化作用
聚合物
有机化学
复合材料
化学
工程类
图层(电子)
作者
Qiqi Zhang,Xin Chen,Zhongshan Yang,Tao Yu,Lequan Liu,Jinhua Ye
标识
DOI:10.1021/acsami.1c19638
摘要
Precisely tailoring the nitrogen defects has been verified to be a promising approach for promoting the photocatalytic efficiency of C3N4. Herein, two-coordinated-N vacancies are selectively introduced into the C3N4 framework by a facile Cl- modification method, whereas its concentration can be facilely tuned by varying Cl- usage in the process of thermal polymerization. Impressively, the optimal defective C3N4 (20 mg) exhibited superior hydrogen and oxygen evolution rates of 48.2 and 21.8 μmol h-1, respectively, in photocatalytic overall water splitting and an apparent quantum efficiency of 6.9% at 420 nm, the highest of reported single-component C3N4 photocatalysts for overall water splitting. Systematic studies including XPS, DFT simulations, and NEXAFS reveal that Cl- modification preferentially facilitates the introduction of two-coordinated-N vacancies through tuning the formation energy and promotes charge carrier separation efficiency, thereby greatly enhancing the photocatalytic efficiency. This work allows for a viable approach to rationally designing defective C3N4 for efficient photocatalysis.
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