Improved photocatalytic property of lignin-derived carbon nanofibers through catalyst synergy

被引:8
|
作者
Zhai, Gongxun [1 ]
Zhou, Jialiang [1 ,2 ]
Xie, Min [1 ]
Jia, Chao [1 ]
Hu, Zexu [1 ]
Xiang, Hengxue [1 ]
Zhu, Meifang [1 ]
机构
[1] Donghua Univ, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Jiangsu Gem Adv Fiber Mat Res Inst Co Ltd, Nantong 226000, Peoples R China
基金
中国国家自然科学基金;
关键词
Lignin; Carbon nanofibers; Photocatalysis; MEMBRANE-SHAPED PHOTOCATALYST; FIBER CLOTH; COMPOSITES; HETEROJUNCTIONS; POLLUTANTS;
D O I
10.1016/j.ijbiomac.2023.123588
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Converting lignin into high value-added products is essential to reduce our dependence on petroleum resources and protect our environment. In this work, TiO2 and g-C3N4 are loaded in the lignin-derived carbon nanofibers (LCNFs) and an efficient LCNFs-based photocatalytic material (TiO2/g-C3N4@LCNFs) is developed. The spinn-ability of lignin solution, the chemical structure and morphology of the LCNFs, and the catalytic degradation property of the TiO2/g-C3N4@LCNFs for Rhodamine B (RhB) are systematically investigated. The TiO2/g-C3N4@LCNFs achieve a 92.76 % degradation rate of RhB under UV-vis irradiation, which is close to or higher than most reported carbon fiber-based photocatalysts. The excellent degradation property of the photocatalysts can be ascribed to the synergy of TiO2 and g-C3N4, which improves the excitation efficiency of electron and hole, and prolongs the lifetime of electron-hole pairs. We envision that our work will provide some guidance for the development of efficient photocatalysts based on biomass-derived fiber materials.
引用
收藏
页数:7
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