Phase segregation reversibility in mixed-metal hydroxide water oxidation catalysts

被引:1
|
作者
Chunguang Kuai
Zhengrui Xu
Cong Xi
Anyang Hu
Zhijie Yang
Yan Zhang
Cheng-Jun Sun
Luxi Li
Dimosthenis Sokaras
Cunku Dong
Shi-Zhang Qiao
Xi-Wen Du
Feng Lin
机构
[1] Virginia Tech,Department of Chemistry
[2] Tianjin University,Institute of New
[3] SLAC National Accelerator Laboratory,Energy Materials, School of Materials Science and Engineering
[4] Argonne National Laboratory,Stanford Synchrotron Radiation Lightsource
[5] The University of Adelaide,Advanced Photon Source
来源
Nature Catalysis | 2020年 / 3卷
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摘要
Achieving stable, low-cost electrocatalysts represents a daunting challenge towards practical water oxidation reactions. Here, we report that a degraded electrocatalyst can be revivified under catalytic operating conditions by manipulating reversible phase segregation. Under the oxygen evolution reaction conditions, Fe segregation develops in the Ni–Fe hydroxide host lattice, with the formation of FeOOH, resulting in an interface between the FeOOH and the host lattice. A dynamic metal dissolution–redeposition process accelerates the Fe segregation and formation of the FeOOH secondary phase, resulting in catalyst deactivation. Operando synchrotron spectroscopic and microscopic analyses suggest that the phase segregation is reversible between the water oxidation potential and the catalyst reduction potential. Therefore, we have developed an intermittent reduction methodology to revivify the catalytic activity under the operating conditions, enhancing catalyst durability. The present study highlights that tailoring phase segregation at the catalyst/electrolyte interface constitutes an important strategy for revivifying and stabilizing catalytic activity.
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页码:743 / 753
页数:10
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