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分子固定在碳纳米管上的钴基活性物种用于氧还原反应

Cobalt-Based Active Species Molecularly Immobilized on Carbon Nanotubes for the Oxygen Reduction Reaction.

作者信息

Kim Sujin, Jang Dawoon, Lim Joonwon, Oh Junghoon, Kim Sang Ouk, Park Sungjin

机构信息

WCSL (World Class Smart Lab) Green Energy Battery Lab., Department of Chemistry and Chemical Engineering, Inha University, Incheon, 22212, Republic of Korea.

National Creative Research Initiative (CRI) Center for Multi-Dimensional, Directed Nanoscale Assembly, Department of Materials Science and Engineering, KAIST, Daejeon, 34141, Republic of Korea.

出版信息

ChemSusChem. 2017 Sep 11;10(17):3473-3481. doi: 10.1002/cssc.201701038. Epub 2017 Aug 16.

Abstract

Hybrid systems in which molecule-based active species are combined with nanoscale materials may offer valuable routes to enhance catalytic performances for electrocatalytic reactions. The development of rationally designed, cost-effective, efficient catalysts for the oxygen reduction reaction (ORR) is a crucial challenge for applications in fuel cells and metal-air batteries. A new hybrid ORR catalyst has been synthesized through a well-defined reaction between Co-based organometallic molecules and N-doped multiwalled carbon nanotubes (MWCNTs) at room temperature. The hybrid ORR catalyst shows excellent catalytic performance with an onset potential of 0.95 V [vs. the reversible hydrogen electrode (RHE)], superior durability, and good methanol tolerance. Chemical and structural characterization after many reaction cycles reveals that the Co-based organometallic species maintained the original structure of cobalt(II) acetylacetonate with coordination to the heteroatoms of the MWCNTs. A thorough electrochemical investigation indicates that the major catalytically active site is Co-O -N .

摘要

将基于分子的活性物种与纳米级材料相结合的混合体系,可能为增强电催化反应的催化性能提供有价值的途径。开发用于氧还原反应(ORR)的合理设计、经济高效的高效催化剂,是燃料电池和金属空气电池应用面临的一项关键挑战。通过在室温下钴基金属有机分子与氮掺杂多壁碳纳米管(MWCNT)之间进行明确的反应,合成了一种新型混合ORR催化剂。该混合ORR催化剂表现出优异的催化性能,起始电位为0.95 V[相对于可逆氢电极(RHE)],具有卓越的耐久性和良好的甲醇耐受性。经过多次反应循环后的化学和结构表征表明,钴基金属有机物种保持了乙酰丙酮钴(II)的原始结构,并与MWCNT的杂原子配位。全面的电化学研究表明,主要的催化活性位点是Co-O-N。

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