光催化
木质素
催化作用
光化学
量子点
硫化镉
配体(生物化学)
电子转移
化学
硫化物
材料科学
纳米技术
组合化学
化学工程
有机化学
无机化学
生物化学
工程类
受体
作者
Xuejiao Wu,Shunji Xie,Chenxi Liu,Cheng Zhou,Jinchi Lin,Jincan Kang,Qinghong Zhang,Zhaohui Wang,Ye Wang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2019-08-02
卷期号:9 (9): 8443-8451
被引量:193
标识
DOI:10.1021/acscatal.9b02171
摘要
Manipulating surface organic ligands has emerged as a useful strategy to enhance the efficiency of heterogeneous catalysts. However, ligand-controlled catalysis for biomass valorization remains unexplored because of the limited knowledge of the ligand functions in heterogeneous catalytic systems involving macromolecules. Here, we report a strong dependence of photocatalytic conversion of native lignin into high-value functionalized aromatics on the ligand attached on cadmium sulfide quantum dots (QDs). The formation of a QD colloidal solution by tuning the hydrophilicity/hydrophobicity of ligands is essential to enable intimate contact between QDs and lignin, leading to high catalytic activity. The surface engineering by manipulating the anchor group and the length of ligands demonstrates that the ligand participates in the electron-transfer process, a crucial step of photocatalysis. The electron decay kinetic study reveals a ligand-mediated electron-tunneling mechanism. These insights offer useful guidance for the design of efficient QD photocatalysts for biomass valorization through ligand modification.
科研通智能强力驱动
Strongly Powered by AbleSci AI