Recent development of efficient electrocatalysts derived from porous organic polymers for oxygen reduction reaction
Science China Chemistry, ISSN: 1869-1870, Vol: 60, Issue: 8, Page: 999-1006
2017
- 42Citations
- 32Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations42
- Citation Indexes42
- 42
- Captures32
- Readers32
- 32
Review Description
Porous organic polymers (POPs) have recently emerged as promising candidates for catalyzing oxygen reduction reaction (ORR). Compared to conventional Pt-based ORR catalysts, these newly developed porous materials, including both non-precious metal based catalysts and metal-free catalysts, are more sustainable and cost-effective. Their porous structures and large surface areas facilitate mass and electron transport and boost the ORR kinetics. This mini-review will give a brief summary of recent development of POPs as electrocatalysts for the ORR. Some design principles, different POP structures, key factors for their ORR catalytic performance, and outlook of POP materials will be discussed.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85025138784&origin=inward; http://dx.doi.org/10.1007/s11426-017-9078-7; http://link.springer.com/10.1007/s11426-017-9078-7; http://link.springer.com/content/pdf/10.1007/s11426-017-9078-7.pdf; http://link.springer.com/article/10.1007/s11426-017-9078-7/fulltext.html; https://dx.doi.org/10.1007/s11426-017-9078-7; https://link.springer.com/article/10.1007/s11426-017-9078-7; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=6041126&internal_id=6041126&from=elsevier
Springer Nature
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