Oxygen vacancy defects engineering on Cu-doped Co3O4 for promoting effective COS hydrolysis

被引:72
作者
Mu, Guanyu [1 ]
Zeng, Yan [1 ]
Zheng, Yong [1 ,2 ]
Cao, Yanning [1 ,2 ]
Liu, Fujian [1 ,2 ]
Liang, Shijing [1 ,2 ]
Zhan, Yingying [1 ,2 ]
Jiang, Lilong [1 ,2 ]
机构
[1] Fuzhou Univ, Natl Engn Res Ctr Chem Fertilizer Catalyst, Fuzhou 350002, Fujian, Peoples R China
[2] Qingyuan Innovat Lab, Quanzhou 362801, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Oxygen vacancy; COS hydrolysis; In situ spectra; Cu doped; Co3O4; CATALYTIC HYDROLYSIS; CARBONYL SULFIDE; ACTIVATED CARBON; MECHANISM; OXIDATION; ADSORPTION; WATER; PERFORMANCE; FLUORIDE; REMOVAL;
D O I
10.1016/j.gee.2021.11.001
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 activation of H2O is a key step of the COS hydrolysis, which may be tuned by oxygen vacancy defects in the catalysts. Herein, we have introduced Cu into Co3O4 to regulate the oxygen vacancy defect content of the catalysts. In situ DRIFTS and XPS spectra reveal that COS and H2O are adsorbed and activated by oxygen vacancy. The 10 at% Cu doped Co3O4 sample (10Cu-Co3O4) exhibits the optimal activity, 100% of COS conversion at 70 degrees C. The improved oxygen vacancies of Cu-Co3O4 accelerate the activation of H2O to form active -OH. COS binds with hydroxyl to form the intermediate HSCO2-, and then the activated -OH on the oxygen vacancy reacts with HSCO2- to form HCO3-. Meanwhile, the catalyst exhibits high catalytic stability because copper species (Cu+/Cu2+) redox cycle mitigate the sulfation of Co3O4 (Co2+/Co3+). Our work offers a promising approach for the rational design of cobalt-related catalysts in the highly efficient hydrolysis COS process. (c) 2021 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:831 / 841
页数:11
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