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Scalable Nickel‐Chelated Polydopamine Conformal Coatings for Enhanced Long‐term Photostability of BiVO 4 Photoanodes
Author(s) -
Qin Weilong,
Liu Qitao,
An Na,
Sun Ruiyuan,
Gong Haorui,
Belachew Neway,
Akbar Muhammad Bilal,
Wang Hao,
Zhou Yang,
Liu Qinglu,
Tang Yunzhi,
Li Jianming,
Le Jiabo,
Kuang Yongbo
Publication year - 2025
Publication title -
energy and environmental materials
Language(s) - English
Resource type - Journals
ISSN - 2575-0356
DOI - 10.1002/eem2.70008
Subject(s) - nickel , scalability , chelation , materials science , term (time) , chemical engineering , optoelectronics , nanotechnology , chemistry , computer science , metallurgy , physics , engineering , quantum mechanics , database
Large‐scale bismuth vanadate (BiVO 4 ) photoanodes are critical to the practical application of photoelectrochemical water splitting devices. However, the lack of interface‐modified coatings with simultaneous low cost, scalability, high hole transport efficiency, low impedance, and photocorrosion resistance is a major challenge that prevents the practical application of large‐size photoanodes. Here, we present a scalable nickel‐chelated polydopamine conformal coating for modifying BiVO 4 (BiVO 4 @PDA‐Ni, BPNi), achieving over 500 h of stable water oxidation at 0.6 V RHE . The excellent stability is attributed to the chelated Ni acting as hole oxidation sites for PDA, thereby suppressing the accumulated‐holes‐induced PDA decomposition. Additionally, the in situ generation of Ni(IV) facilitates the structural reorganization of PDA in the photoelectrochemical system, further enhancing the stability of the PDA matrix. The findings of PDA photodegradation, its autonomous metal ion capture within photoelectrochemical systems, and the rapid deactivation of BPNi photoanodes caused by vanadium (V) ions have all provided significant guidance for the enhancement of PDA. Our study demonstrates that nickel‐chelated polydopamine can be applied to large‐scale BiVO 4 photoanodes to facilitate oxygen evolution. This will promote the development of large‐scale photoanodes suitable for photoelectrochemical devices.

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