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In situ decomposition of metal-organic frameworks into ultrathin nanosheets for the oxygen evolution reaction

The oxygen evolution reaction (OER) is a pivotal process for water-splitting and many other energy technologies involving oxygen electrodes. Herein, a new synthesis strategy is proposed to prepare OER catalysts based on a simple yet flexible in situ decomposition of Co-based acetate hydroxide metal-...

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Bibliographic Details
Published in:Nano research 2016-06, Vol.9 (6), p.1856-1865
Main Authors: He, Kai, Cao, Zhen, Liu, Ruirui, Miao, Ya, Ma, Houyi, Ding, Yi
Format: Article
Language:English
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Summary:The oxygen evolution reaction (OER) is a pivotal process for water-splitting and many other energy technologies involving oxygen electrodes. Herein, a new synthesis strategy is proposed to prepare OER catalysts based on a simple yet flexible in situ decomposition of Co-based acetate hydroxide metal-organic frameworks (MOFs). This process allows straightforward fabrication of various 2D hydroxide ultrathin nanosheets (UNSs) with excellent component controllability. The as-obtained Co-based hydroxide UNSs demonstrate superior catalytic activity for the OER due to the exposure of numerous active sites. In particular, the CoNi hydroxide UNSs exhibit low overpotentials (r/) of 324 and 372 mV at current densities of 10 and 100 mA-cm-2, respectively; a large turnover frequency (TOF) of 0.16 s-~ at T/= 380 mV; and a small Tafel slope of 33 mV.dec-~ in an alkaline environment. Importantly, these values are superior to those of the state-of-the- art IrO2 commercial electrocatalyst. This facile strategy enables the exploration of more efficient and economic OER electrocatalysts with various constituents and opens a promising avenue for large-scale fabrication of functional nanocatalysts for use in clean ener~:v technologies.
ISSN:1998-0124
1998-0000
DOI:10.1007/s12274-016-1078-x