Spatial decoupling of dehydrogenation and CO oxidation by Ni-Co-Ti hierarchical trimetallic catalyst for electrocatalytic oxidation of methanol

被引:23
|
作者
Zhao, Shenghao [1 ]
Wang, Tianqi [1 ]
Ji, Zhijiao [1 ]
Song, Yajun [1 ]
Li, Yi [1 ,2 ,3 ]
Liu, Jia [1 ,4 ,5 ]
Hu, Wenping [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Sch Sci, Dept Chem, Tianjin Key Lab Mol Optoelect, Tianjin 300072, Peoples R China
[2] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
[3] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[4] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
[5] Yulin Univ, Yulin 719000, Shanxi, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 320卷
关键词
Methanol electrooxidation; Hierarchical catalyst; Spatial decoupling; Mass transfer; COBALT; CARBON; ELECTROOXIDATION; NANOPARTICLES; NANOSHEET; GRAPHENE; SUPPORT;
D O I
10.1016/j.apcatb.2022.122024
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
Methanol electro-oxidation reaction (MOR) is the kernel of methanol fuel cell. When the multi-step microscopic transformations process of MOR couples and occurs on the same active site, undoubtedly it reduces the proba-bility of reaction and increases the steric hindrance, resulting in slow reaction kinetics and degradation of cat-alytic performance. In order to decouple the dehydrogenation and CO oxidation in MOR, herein we synthesized the hierarchical catalyst (NiCo/N-TiO2 @NaOH) with bifunctional spatial distribution, which displayed 73 mA cm-2 at the potential of 1.5 V (vs. RHE) and only 20 % degradation of performance after continuously elec-trolysis over 40,000 s. Based on analysis of mass transfer and electron transport in hierarchical structure, combining with in-situ mass spectrometry and theory calculation, the high MOR performance of NiCo/N-TiO2 can be ascribed to the spatial decoupling the MOR reactions including dehydrogenation under synergic effect of Ni/Co and CO oxidation on N-TiO2 film.
引用
收藏
页数:9
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