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Meta-organic-framework-derived fe-n/c electrocatalyst with five-coordinated fe-n-x), sites for advanced oxygen reduction in acid media

文献类型:期刊论文

作者Lai, Qingxue1; Zheng, Lirong2; Liang, Yanyu1,3; He, Jianping1; Zhao, Jingxiang4; Chen, Junhong5
刊名Acs catalysis
出版日期2017-03-01
卷号7期号:3页码:1655-1663
关键词Host guest chemistry Confinement effect Fe-n-x sites Five-coordinated configuration Oxygen reduction Electrocatalytic mechanism
ISSN号2155-5435
DOI10.1021/acscatal.6b02966
通讯作者Liang, yanyu(liangyy403@l26.com) ; Chen, junhong(jhchen@uwm.edu)
英文摘要Even though fe-n/c electrocatalysts with abundant fe-n-x active sites have been developed as one of the most promising alternatives to precious metal materials for oxygen reduction reaction (orr), further improvement of their performance requires precise control over fe-n-x sites at the molecular level and deep understanding of the catalytic mechanism associated with each particular structure. herein, we report a host guest chemistry strategy to construct fe-mim nanocluster (nc) (guest)@zeolite imidazole framework 8 (zif-8) (host) precursors that can be transformed into fe-n/c electrocatalysts with controllable structures. the zif-8 host network exhibits a significant host guest relationship dependent confinement effect for the pyrolysis process, resulting in different types of fe-nx sites with two- to five-coordinated configurations on the porous carbon matrix confirmed by x-ray absorption near edge structure ()canes) and fourier transform (ft) extended x-ray absorption fine structure (exafs) spectra. electrochemical tests reveal that the five-coordinated fe-n-x sites can significantly promote the reaction rate in acid media, due to the small orr energy barrier and the low adsorption energy of intermediate oh on these sites suggested by density functional theory (dft) calculations. such a synthesis strategy provides an effective route to realize the controllable construction of highly active sites for orr at the molecular level.
WOS关键词IRON-BASED CATALYSTS ; MEMBRANE FUEL-CELLS ; FE/N/C-CATALYSTS ; ACTIVE-SITES ; ELECTROREDUCTION ; PHTHALOCYANINE ; POLYANILINE
WOS研究方向Chemistry
WOS类目Chemistry, Physical
语种英语
WOS记录号WOS:000395726500018
出版者AMER CHEMICAL SOC
URI标识http://www.irgrid.ac.cn/handle/1471x/2176699
专题高能物理研究所
通讯作者Liang, Yanyu; Chen, Junhong
作者单位1.Nanjing Univ Aeronaut & Astronaut, Coll Mat Sci & Technol, Jiangsu Key Lab Mat & Technol Energy Convers, Nanjing 210016, Peoples R China
2.Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing 100049, Peoples R China
3.Jiangsu Collaborat Innovat Ctr Adv Inorgan Funct, Nanjing 211816, Jiangsu, Peoples R China
4.Harbin Normal Univ, Coll Chem & Chem Engn, Harbin 150025, Peoples R China
5.Univ Wisconsin, Dept Mech Engn, Milwaukee, WI 53211 USA
推荐引用方式
GB/T 7714
Lai, Qingxue,Zheng, Lirong,Liang, Yanyu,et al. Meta-organic-framework-derived fe-n/c electrocatalyst with five-coordinated fe-n-x), sites for advanced oxygen reduction in acid media[J]. Acs catalysis,2017,7(3):1655-1663.
APA Lai, Qingxue,Zheng, Lirong,Liang, Yanyu,He, Jianping,Zhao, Jingxiang,&Chen, Junhong.(2017).Meta-organic-framework-derived fe-n/c electrocatalyst with five-coordinated fe-n-x), sites for advanced oxygen reduction in acid media.Acs catalysis,7(3),1655-1663.
MLA Lai, Qingxue,et al."Meta-organic-framework-derived fe-n/c electrocatalyst with five-coordinated fe-n-x), sites for advanced oxygen reduction in acid media".Acs catalysis 7.3(2017):1655-1663.

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