Mechanism study of the photothermal function of lignin: the effect of electron-withdrawing groups

被引:18
|
作者
Lei, Junjie [1 ]
Chen, Liheng [2 ]
Lin, Jinxin [2 ]
Liu, Weifeng [1 ]
Xiong, Qingang [3 ]
Qiu, Xueqing [2 ]
机构
[1] South China Univ Technol, Sch Chem & Chem Engn, State Key Lab Pulp & Paper Engn, Guangdong Prov Key Lab Green Chem Prod Technol, Guangzhou 510640, Peoples R China
[2] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China
[3] South China Univ Technol, State Key Lab Pulp & Paper Engn, Guangzhou 510640, Peoples R China
基金
中国国家自然科学基金;
关键词
PERFORMANCE; SOLVENT;
D O I
10.1039/d3gc04125e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As a new type of green photothermal material, lignin exhibits an excellent photothermal effect due to its abundant aromatic rings and pi-pi conjugated structure. To develop value-added applications of lignin in the photothermal field, it is important to explore strategies for regulating the photothermal conversion of lignin. In this work, the photothermal effect of lignin was improved significantly through modification with an electron-withdrawing group. The introduction of acetyl resulted in the formation of an electron donor-acceptor (D-A) structure in lignin and enhanced the light absorption ability. The intermolecular interaction among lignin molecules also decreased after modification with acetyl groups, leading to enhanced non-radiative decay induced by molecular motion. Under 808 nm laser irradiation at 0.51 W cm-2, the photothermal conversion efficiency of acetylated lignin (ACAL) reached as high as 73.2%, which was 37% higher than that of unmodified lignin. This study provides a new strategy to enhance the photothermal effect of lignin and deepens the understanding of the lignin photothermal mechanism. The photothermal effect of lignin was significantly enhanced by introducing electron-withdrawing group attributing to the improved light absorption by electron donor-acceptor structure and the enhanced non-radiative decay through molecular motion.
引用
收藏
页码:2143 / 2156
页数:14
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