Engineering S-scheme mCN@mPDIP molecular heterojunction with highly efficient interface charge transfer for photocatalytic aerobic oxidation synthesis

被引:0
|
作者
Nie, Yina [1 ]
Ma, Yang-Ai [1 ]
Wei, Lele [1 ]
Wu, Mingxia [1 ]
Zhao, Xia [2 ]
Liu, Lin [1 ]
Wan, Jun [1 ]
机构
[1] Yanan Univ, Res Inst Comprehens Energy Ind Technol, Coll Chem & Chem Engn, Shaanxi Key Lab Chem React Engn, Yanan 716000, Peoples R China
[2] Shaanxi Univ Technol, Sch Chem & Environm Sci, Shaanxi Key Lab Catalysis, Hanzhong 723001, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Molecular heterojunction; S -scheme heterojunction; Interface charge transfer; Aerobic oxidation of sulfides; CARBON NITRIDE; SULFIDES; SULFOXIDES;
D O I
10.1016/j.jcis.2024.08.014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The construction of S-scheme heterojunctions, which offers a promising approach for spatially separating photogenerated charge carriers with high redox potentials and multimolecular activation, represents a viable modification strategy in photocatalytic applications. However, the prevalent insufficient contact areas between two components result in low interface charge transfer efficiency, thereby impeding the photocatalytic performance of such heterostructures. Herein, we address this limitation by introducing a unique mCN@mPDIP molecular heterojunction through a pH-triggered molecule self-assembly eutectoid technique, enabling intimate interface contact and promoting highly efficient interfacial charge transfer following an S-scheme mechanism. Consequently, the mCN@mPDIP molecular heterojunction achieves significantly improved charge separation efficiency and higher concentration of active carriers compared to typical bCN-bPDIP bulk heterojunction and nCN/nPDIP nano heterojunction. Combined with the effective sulfide activation on mPDIP sites and O2 activation on mCN sites, the resulting mCN@mPDIP demonstrates outstanding activity in the photocatalytic aerobic oxidation of sulfides into sulfoxides without any redox mediators.
引用
收藏
页码:873 / 882
页数:10
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