Plasma induced Fe-NX active sites to improve the oxygen reduction reaction performance

Peng Rao , Tian-Jiao Wang , Jing Li , Pei-Lin Deng , Yi-Jun Shen , Yu Chen , Xin-Long Tian
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引用次数: 28

Abstract

Rational design of high-efficient and low-cost catalysts as alternatives to Pt-based catalysts toward the oxygen reduction reaction (ORR) is extremely desirable but challenging. In this work, Fe@NCNT is firstly synthesized via the one-pot pyrolysis method, then Fe-NX active species are in-situ created on the prepared Fe@NCNT by a feasible “plasma inducing” strategy to synthesize the resulting catalyst (Fe@NCNT-P) for ORR. The morphology of Fe@NCNT-P is perfectly inherited by the derived carbon precursor, resulting in the core-shell structure of carbon-coated Fe and a mesoporous dominant nanostructure with a high specific surface area of 536 m2 g−1. The resultant Fe@NCNT-P catalyst exhibits remarkable ORR activity and durability, as well as outstanding performance in assembled zinc-air battery (ZAB) test with a peak power density of 240 mW cm−2. This work not only reports a novel and robust ORR catalyst, but also proposes a simple and effective strategy to improve the ORR electrocatalytic performance.

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等离子体诱导Fe-NX活性位点,提高氧还原反应性能
合理设计高效、低成本的催化剂替代pt基催化剂用于氧还原反应(ORR)是非常可取的,但也具有挑战性。本文首先采用一锅热解法合成Fe@NCNT,然后采用可行的“等离子体诱导”策略在制备好的Fe@NCNT上原位生成Fe-NX活性物质,合成ORR催化剂(Fe@NCNT-P)。Fe@NCNT-P的形貌被衍生的碳前驱体完美地继承,形成了碳包覆铁的核壳结构和具有536 m2 g−1的高比表面积的介孔优势纳米结构。所得Fe@NCNT-P催化剂表现出良好的ORR活性和耐久性,在组装锌-空气电池(ZAB)测试中表现优异,峰值功率密度为240 mW cm - 2。本工作不仅报道了一种新颖而坚固的ORR催化剂,而且提出了一种简单有效的提高ORR电催化性能的策略。
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