中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A pyrolysis-free path toward superiorly catalytic nitrogen-coordinated single atom

文献类型:期刊论文

作者Peng, Peng2; Shi, Lei2; Huo, Feng1; Mi, Chunxia2; Wu, Xiaohong1,3; Zhang, Suojiang1; Xiang, Zhonghua2
刊名SCIENCE ADVANCES
出版日期2019-08-01
卷号5期号:8页码:7
ISSN号2375-2548
DOI10.1126/sciadv.aaw2322
英文摘要[ Nitrogen-coordinated single-atom catalysts (SACs) have emerged as a frontier for electrocatalysis (such as oxygen reduction) with maximized atom utilization and highly catalytic activity. The precise design and operable synthesis of SACs are vital for practical applications but remain challenging because the commonly used high-temperature treatments always result in unpredictable structural changes and randomly created single atoms. Here, we develop a pyrolysis-free synthetic approach to prepare SACs with a high electrocatalytic activity using a fully pi-conjugated iron phthalocyanine (FePc)-rich covalent organic framework (COF). Instead of randomly creating Fe-nitrogen moieties on a carbon matrix (Fe-N-C) through pyrolysis, we rivet the atomically well-designed Fe-N-C centers via intermolecular interactions between the COF network and the graphene matrix. The as-synthesized catalysts demonstrate exceptional kinetic current density in oxygen reduction catalysis (four times higher than the benchmark Pt/C) and superior power density and cycling stability in Zn-air batteries compared with Pt/C as air electrodes.
WOS关键词OXYGEN REDUCTION REACTION ; COVALENT ORGANIC POLYMERS ; N-C CATALYST ; EFFICIENT ELECTROCATALYSTS ; DURABLE ELECTROCATALYST ; FE-N/C ; SITES ; CARBON ; IRON ; PERFORMANCE
资助项目National Key Research and Development Program of China[2017YFA0206500] ; Natural Science Foundation of China[21676020] ; Natural Science Foundation of China[21606232] ; Beijing Natural Science Foundation[17L20060] ; Fundamental Research Funds for the Central Universities[buctrc201420] ; Fundamental Research Funds for the Central Universities[buctrc201714] ; BUCT Fund for Disciplines Construction and Development[XK1502] ; Young Elite Scientists Sponsorship Program by CAST[2017QNRC001] ; Talent cultivation and open project of State Key Laboratory of Organic-Inorganic Composites[OIC-201801007] ; Distinguished Scientist Program at BUCT[buctylkxj02] ; "111" Project of China[B14004]
WOS研究方向Science & Technology - Other Topics
语种英语
WOS记录号WOS:000481798400022
出版者AMER ASSOC ADVANCEMENT SCIENCE
资助机构National Key Research and Development Program of China ; Natural Science Foundation of China ; Beijing Natural Science Foundation ; Fundamental Research Funds for the Central Universities ; BUCT Fund for Disciplines Construction and Development ; Young Elite Scientists Sponsorship Program by CAST ; Talent cultivation and open project of State Key Laboratory of Organic-Inorganic Composites ; Distinguished Scientist Program at BUCT ; "111" Project of China
源URL[http://ir.ipe.ac.cn/handle/122111/30571]  
专题中国科学院过程工程研究所
通讯作者Xiang, Zhonghua
作者单位1.Chinese Acad Sci, CAS Key Lab Green Proc & Engn, State Key Lab Multiphase Complex Syst, Inst Proc Engn,Beijing Key Lab Ion Liquids Clean, Beijing 100190, Peoples R China
2.Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
3.Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Peng, Peng,Shi, Lei,Huo, Feng,et al. A pyrolysis-free path toward superiorly catalytic nitrogen-coordinated single atom[J]. SCIENCE ADVANCES,2019,5(8):7.
APA Peng, Peng.,Shi, Lei.,Huo, Feng.,Mi, Chunxia.,Wu, Xiaohong.,...&Xiang, Zhonghua.(2019).A pyrolysis-free path toward superiorly catalytic nitrogen-coordinated single atom.SCIENCE ADVANCES,5(8),7.
MLA Peng, Peng,et al."A pyrolysis-free path toward superiorly catalytic nitrogen-coordinated single atom".SCIENCE ADVANCES 5.8(2019):7.

入库方式: OAI收割

来源:过程工程研究所

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