杂原子
氮化碳
光催化
分解水
材料科学
罗丹明B
X射线光电子能谱
制氢
氢
碳纤维
石墨氮化碳
掺杂剂
析氧
光化学
光催化分解水
兴奋剂
化学
催化作用
化学工程
光电子学
物理化学
有机化学
电极
戒指(化学)
复合材料
工程类
复合数
电化学
作者
Yabin Jiang,Shaofan Fang,Chen Cao,Enna Hong,Lei Zeng,Wensheng Yang,Limin Huang,Chunzhen Yang
标识
DOI:10.1016/j.jcis.2021.12.077
摘要
Solar-driven water splitting has been regarded as a promising strategy for renewable hydrogen production. Among many semiconductor photocatalysts, graphitic carbon nitride (g-C3N4) has received tremendous attention due to its two-dimensional structure, appropriate band gap and decent photocatalytic activity. However, it suffers severe charge recombination problems, affecting its practical performance. In this work, we demonstrated that dual heteroatoms (C and O) doped g-C3N4 can exhibit about 3 times higher catalytic performance for hydrogen evolution than that of the normal g-C3N4 with a hydrogen evolution rate reaching 2595.4 umol g-1h-1 and an apparent quantum efficiency at 420 nm of 16.6%. The heteroatoms (C and O) doped g-C3N4 photocatalyst also exhibited superior removal performance when removing Rhodamine B (RhB) . X-ray photoelectron spectroscopy (XPS), solid-state nuclear magnetic resonance (ssNMR) and X-ray absorption near-edge structure (XANES) spectroscopy reveal that the carbon and oxygen dopants replace the sp2 nitrogen and bridging N atom, respectively. DFT calculations demonstrate the codoping of carbon and oxygen- induced the generation of mid-gap state, leading to the improvement of light harvesting and charge separation.
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