Rapid room-temperature synthesis of nanocrystalline spinels as oxygen reduction and evolution electr

Author:  ["Fangyi Cheng","Jian Shen","Bo Peng","Yuede Pan","Zhanliang Tao","Jun Chen"]

Publication:  Nature Chemistry

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Tags:     Chemistry

Abstract

Spinels can serve as alternative low-cost bifunctional electrocatalysts for oxygen reduction/evolution reactions (ORR/OER), which are the key barriers in various electrochemical devices such as metal–air batteries, fuel cells and electrolysers. However, conventional ceramic synthesis of crystalline spinels requires an elevated temperature, complicated procedures and prolonged heating time, and the resulting product exhibits limited electrocatalytic performance. It has been challenging to develop energy-saving, facile and rapid synthetic methodologies for highly active spinels. In this Article, we report the synthesis of nanocrystalline MxMn3–xO4 (M = divalent metals) spinels under ambient conditions and their electrocatalytic application. We show rapid and selective formation of tetragonal or cubic MxMn3–xO4 from the reduction of amorphous MnO2 in aqueous M2+ solution. The prepared CoxMn3–xO4 nanoparticles manifest considerable catalytic activity towards the ORR/OER as a result of their high surface areas and abundant defects. The newly discovered phase-dependent electrocatalytic ORR/OER characteristics of Co–Mn–O spinels are also interpreted by experiment and first-principle theoretical studies. Ceramic preparation of spinels — materials useful for a wide range of applications — requires complicated procedures and heat treatment over long periods. Now, it is shown that rapid synthesis of nanocrystalline Co–Mn–O spinels can be achieved under ambient conditions, and the resulting nanoparticles exhibit considerable catalytic activity towards the electrochemical oxygen reduction/evolution reactions.

Cite this article

Cheng, F., Shen, J., Peng, B. et al. Rapid room-temperature synthesis of nanocrystalline spinels as oxygen reduction and evolution electrocatalysts. Nature Chem 3, 79–84 (2011). https://doi.org/10.1038/nchem.931

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