中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Geometric Occupancy and Oxidation State Requirements of Cations in Cobalt Oxides for Oxygen Reduction Reaction

文献类型:期刊论文

作者Liu, Jing1; Bao, Hongliang2; Zhang, Bingsen3; Hua, Qingfeng1; Shang, Mingfeng2; Wang, Jianqiang2; Jiang, Luhua1
刊名ACS APPLIED MATERIALS & INTERFACES
出版日期2019-04-03
卷号11期号:13页码:12525-12534
ISSN号1944-8244
关键词cobalt oxide oxygen reduction reaction geometric occupancy valance state octahedral coordination
DOI10.1021/acsami.9b00481
通讯作者Wang, Jianqiang(wangjianqiang@sinap.ac.cn) ; Jiang, Luhua(luhuajiang@qust.edu.cn)
英文摘要Cobalt oxides, including spinel Co3O4 and rock-salt CoO, have been widely reported as promising catalysts for oxygen reduction reaction (ORR). However, three types of cobalt ions, i.e., Co2+ in the tetrahedral site (Co-Td(2+)), Co3+ in the octahedral site (Co-Oh(3+)), and Co2+ in the octahedral site (Co-Oh(2+)), are included in these oxides, and the roles of cobalt geometric occupancy and valance states have remained elusive. Here, for the first time, we investigated the effects of cobalt geometric occupancy on the ORR activity by substituting Co-Td(2+) and Co-Oh(3+) of Co3O4 with inactive Zn2+ and Al3+, respectively. The ORR activity decreases in the order of Co3O4 (Co-Oh(3+), Co-Td(2+)) < ZnCo2O4 (Co-Oh(3+)) << CoAl2O4 (Co-Td(2+)) in accordance with the ORR overpotentials at the current density of 0.1 mA cm(Ox)(-2). Furthermore, by comparatively investigating the activity and stability of Co3O4 (Co-Oh(3+)) and CoO (Co-Oh(2+)) nanoparticles, by virtue of the electrochemical technique, the high-resolution transmission electron microscopy, and the in operando fuel cell-X-ray absorption spectroscopy techniques, it was revealed that Co-Oh(2+), in CoO is the main active site, which under electrochemical conditions tends to transform into Co-Oh(3+), and form Co3O4 with a hollow structure due to the Kirkendall effect; nevertheless, it retains decent ORR activity due to the formation of the unique hollow structure.
资助项目Key Research and Development Project of Shandong Province[2017GGX20107] ; National Science Foundation of China[21776146] ; National Science Foundation of China[21576258] ; Taishan Scholars special project funding of Shandong Province[ts201712046]
WOS研究方向Science & Technology - Other Topics ; Materials Science
语种英语
出版者AMER CHEMICAL SOC
WOS记录号WOS:000463843900039
资助机构Key Research and Development Project of Shandong Province ; National Science Foundation of China ; Taishan Scholars special project funding of Shandong Province
源URL[http://ir.imr.ac.cn/handle/321006/132782]  
专题金属研究所_中国科学院金属研究所
通讯作者Wang, Jianqiang; Jiang, Luhua
作者单位1.Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Nanomat & Electrocatalysis Lab, 53 Zhengzhou Rd, Qingdao 266042, Shandong, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Appl Phys, 239 Zhangheng Rd, Shanghai 201204, Peoples R China
3.Chinese Acad Sci, Inst Met Res, 72 Wenhua Rd, Shenyang 110016, Liaoning, Peoples R China
推荐引用方式
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Liu, Jing,Bao, Hongliang,Zhang, Bingsen,et al. Geometric Occupancy and Oxidation State Requirements of Cations in Cobalt Oxides for Oxygen Reduction Reaction[J]. ACS APPLIED MATERIALS & INTERFACES,2019,11(13):12525-12534.
APA Liu, Jing.,Bao, Hongliang.,Zhang, Bingsen.,Hua, Qingfeng.,Shang, Mingfeng.,...&Jiang, Luhua.(2019).Geometric Occupancy and Oxidation State Requirements of Cations in Cobalt Oxides for Oxygen Reduction Reaction.ACS APPLIED MATERIALS & INTERFACES,11(13),12525-12534.
MLA Liu, Jing,et al."Geometric Occupancy and Oxidation State Requirements of Cations in Cobalt Oxides for Oxygen Reduction Reaction".ACS APPLIED MATERIALS & INTERFACES 11.13(2019):12525-12534.

入库方式: OAI收割

来源:金属研究所

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