File Download

There are no files associated with this item.

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.conferencePlace KO -
dc.citation.conferencePlace 제주도, 제주국제컨벤션센터 -
dc.citation.title 2016 Fall Korean Society of Industrial and Engineering Chemistry Meeting -
dc.contributor.author Joo, Sang Hoon -
dc.date.accessioned 2023-12-19T19:41:09Z -
dc.date.available 2023-12-19T19:41:09Z -
dc.date.created 2017-01-08 -
dc.date.issued 2016-10-28 -
dc.description.abstract The development of highly active, durable, and low-cost oxygen reduction reaction (ORR) catalysts is central to making polymer electrolyte fuel cells (PEFCs) commercially viable. In this context, tremendous recent efforts have been devoted to replacing expensive, scarce Pt-based electrocatalysts with non-precious metal or metal-free materials for the ORR. Among the classes of potential electrocatalysts, transition metal and heteroatom such as nitrogen co-doped carbon structures (M-N/C ; M=Fe and or Co) represent most promising catalytic activity, approaching that of Pt-based catalysts. During the last few years, our group has endeavored to develop high-performance M-N/C electrocatalysts for the ORR. In this presentation, design, preparation, and molecular-level characterization of new M-N/C catalysts and their implementation in PEFCs will be presented. -
dc.identifier.bibliographicCitation 2016 Fall Korean Society of Industrial and Engineering Chemistry Meeting -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/40156 -
dc.identifier.url http://www.ksiec.or.kr/suite/_KSIEC/conference/PaperDetail.php?pid=23900 -
dc.language 영어 -
dc.publisher 한국공업화학회 -
dc.title Strategies for High-Performance Non-Precious Metal Oxygen Reduction Reaction Catalysts -
dc.type Conference Paper -
dc.date.conferenceDate 2016-10-26 -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.