光催化
异质结
材料科学
石墨氮化碳
复合数
化学工程
多孔性
纳米技术
氮化物
催化作用
光电子学
复合材料
化学
图层(电子)
生物化学
工程类
作者
Genrui Zhang,Xiaojing Li,Na Li,Tingting Wu,Lei Wang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2023-03-05
卷期号:16 (5): 6568-6576
被引量:18
标识
DOI:10.1007/s12274-022-5352-6
摘要
Constructing 2D/2D face-to-face heterojunctions is believed to be an effective strategy to enhance photocatalytic performance due to the enlarged contact interface and increased surface active sites. Herein, 2D porous NiCo oxyphosphide (NiCoOP) was synthesized for the first time and coupled with graphitic carbon nitride (g-C3N4) nanosheets to form 2D/2D heterojunctions via an in-situ phosphating method. The optimal 4 wt.% 2D/2D NiCoOP/g-C3N4 (OPCN) photocatalyst achieves a hydrogen evolution rate of 1.4 mmol·h−1·g−1, which is 33 times higher than that of pure g-C3N4. The greatly improved photocatalytic performance of the composite photocatalysts could be attributed to the formation of interfacial surface bonding states and sufficient charge transfer channels for accelerating carrier separation and transfer and the porous structure of NiCoOP nanosheets with abundant surface active sites for promoting surface reactions. Amazingly, the 2D/2D OPCN composite photocatalysts also exhibit superior stability during photocatalytic reactions. This study not only designs new noble-metal-free NiCoOP/g-C3N4 composite photocatalysts but also provides a new sight in fabricating face-to-face 2D/2D heterojunctions for their application in energy conversion areas.
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