Controllable electronic effect via deep eutectic solvents modification for boosted aerobic oxidative desulfurization

被引:7
|
作者
Lu, Linjie [1 ]
Zhang, Bingsen [2 ]
Li, Hongping [1 ]
Chao, Yanhong [3 ]
Li, Yujun [1 ]
Chen, Linlin [1 ]
Li, Huaming [1 ]
Ji, Hongbing [1 ,4 ]
Wu, Peiwen [1 ]
Zhu, Wenshuai [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Jiangsu, Peoples R China
[2] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[3] Jiangsu Univ, Sch Pharm, Zhenjiang 212013, Jiangsu, Peoples R China
[4] Sun Yat sen Univ, Sch Chem, Fine Chem Ind Res Inst, Guangzhou 510275, Peoples R China
来源
MOLECULAR CATALYSIS | 2021年 / 512卷
关键词
Electronic structure; Deep eutectic solvent; Hexagonal boron nitride; Organic modification; Oxidative desulfurization; METAL-SUPPORT INTERACTIONS; HEXAGONAL BORON-NITRIDE; CATALYST; DEHYDROGENATION; SELECTIVITY; DESS; ODS;
D O I
10.1016/j.mcat.2021.111757
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
Tuning electronic structure of metal catalysts by organic modification is an efficient strategy for domination of their catalytic performances. However, the electronic structure tuning over metal-free catalysts remains to be a challenge. In this work, an organic modification strategy with deep eutectic solvents (DES) as organic modifier over metal-free catalysts was proposed to tune the electronic structure of hexagonal boron nitride (h-BN). Detailed experiments showed that the electronic properties of h-BN was rationally tuned by the introduced DES, in which the B atoms in h-BN were positively charged. Meanwhile, the modulated electronic properties can lower the activation energy for the generation of hydroxyl radicals (center dot OH) from hydrogen peroxide (H2O2), thus leading to a promoted catalytic performance in oxidative desulfurization. This finding may pave a new strategy for tuning metal-free catalysts with highly-active catalytic performance.
引用
收藏
页数:8
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