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A self-healing catalyst for electrocatalytic and photoelectrochemical oxygen evolution in highly alkaline conditions

While self-healing is considered a promising strategy to achieve long-term stability for oxygen evolution reaction (OER) catalysts, this strategy remains a challenge for OER catalysts working in highly alkaline conditions. The self-healing of the OER-active nickel iron layered double hydroxides (NiF...

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Detalles Bibliográficos
Autores principales: Feng, Chao, Wang, Faze, Liu, Zhi, Nakabayashi, Mamiko, Xiao, Yequan, Zeng, Qiugui, Fu, Jie, Wu, Qianbao, Cui, Chunhua, Han, Yifan, Shibata, Naoya, Domen, Kazunari, Sharp, Ian D., Li, Yanbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514436/
https://www.ncbi.nlm.nih.gov/pubmed/34645825
http://dx.doi.org/10.1038/s41467-021-26281-0
Descripción
Sumario:While self-healing is considered a promising strategy to achieve long-term stability for oxygen evolution reaction (OER) catalysts, this strategy remains a challenge for OER catalysts working in highly alkaline conditions. The self-healing of the OER-active nickel iron layered double hydroxides (NiFe-LDH) has not been successful due to irreversible leaching of Fe catalytic centers. Here, we investigate the introduction of cobalt (Co) into the NiFe-LDH as a promoter for in situ Fe redeposition. An active borate-intercalated NiCoFe-LDH catalyst is synthesized using electrodeposition and shows no degradation after OER tests at 10 mA cm(−2) at pH 14 for 1000 h, demonstrating its self-healing ability under harsh OER conditions. Importantly, the presence of both ferrous ions and borate ions in the electrolyte is found to be crucial to the catalyst’s self-healing. Furthermore, the implementation of this catalyst in photoelectrochemical devices is demonstrated with an integrated silicon photoanode. The self-healing mechanism leads to a self-limiting catalyst thickness, which is ideal for integration with photoelectrodes since redeposition is not accompanied by increased parasitic light absorption.