Dual doping: An emerging strategy to construct efficient metal catalysts for water electrolysis

Chen, Z; Han, N; Wei, W; Chu, D; Ni, B

Dual doping: An emerging strategy to construct efficient metal catalysts for water electrolysis

Chen, Z Han, N Wei, W

Chu, D Ni, B

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Publisher:: Wiley
Publication Type:: Journal Article
Citation:: EcoEnergy, 2024, 2, (1), pp. 114-140
Issue Date:: 2024-03

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Field	Value	Language
dc.contributor.author	Chen, Z
dc.contributor.author	Han, N
dc.contributor.author	Wei, W https://orcid.org/0000-0001-5613-337X
dc.contributor.author	Chu, D
dc.contributor.author	Ni, B
dc.date.accessioned	2025-03-31T05:19:02Z
dc.date.available	2025-03-31T05:19:02Z
dc.date.issued	2024-03
dc.identifier.citation	EcoEnergy, 2024, 2, (1), pp. 114-140
dc.identifier.issn	2835-9380
dc.identifier.issn	2835-9399
dc.identifier.uri	http://hdl.handle.net/10453/186363
dc.description.abstract	<jats:title>Abstract</jats:title><jats:p>Developing efficient electrocatalysts for water electrolysis is critical for sustainable hydrogen energy development. For enhancing the catalytic performance of metal catalysts, dual doping has attracted enormous interest for its high effectiveness and facile realization. Dual doping is effective for tuning the electronic properties, enhancing the electrical conductivity, populating active sites, and improving the stability of metal catalysts. In this review, recent developments in cation–cation, cation–anion, and anion–anion dual‐doped catalysts for water splitting are comprehensively summarized and discussed. An emphasis is put on illustrating how dual doping regulates the external and internal properties and boosts the catalytic performance of catalysts. Additionally, perspectives are pointed out to guide future research on engineering high‐performance heteroatom‐doped electrocatalysts.</jats:p>
dc.language	en
dc.publisher	Wiley
dc.relation	http://purl.org/au-research/grants/arc/DP220101139
dc.relation	http://purl.org/au-research/grants/arc/DP220101139
dc.relation.ispartof	EcoEnergy
dc.relation.isbasedon	10.1002/ece2.29
dc.rights	info:eu-repo/semantics/openAccess
dc.title	Dual doping: An emerging strategy to construct efficient metal catalysts for water electrolysis
dc.type	Journal Article
utslib.citation.volume	2
pubs.organisational-group	University of Technology Sydney
pubs.organisational-group	University of Technology Sydney/Faculty of Engineering and Information Technology
pubs.organisational-group	University of Technology Sydney/Faculty of Engineering and Information Technology/School of Civil and Environmental Engineering
pubs.organisational-group	University of Technology Sydney/UTS Groups
pubs.organisational-group	University of Technology Sydney/UTS Groups/Centre for Technology in Water and Wastewater (CTWW)
utslib.copyright.status	open_access	*
dc.rights.license	This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/
dc.date.updated	2025-03-31T05:19:00Z
pubs.issue	1
pubs.publication-status	Published
pubs.volume	2
utslib.citation.issue	1

Abstract:

AbstractDeveloping efficient electrocatalysts for water electrolysis is critical for sustainable hydrogen energy development. For enhancing the catalytic performance of metal catalysts, dual doping has attracted enormous interest for its high effectiveness and facile realization. Dual doping is effective for tuning the electronic properties, enhancing the electrical conductivity, populating active sites, and improving the stability of metal catalysts. In this review, recent developments in cation–cation, cation–anion, and anion–anion dual‐doped catalysts for water splitting are comprehensively summarized and discussed. An emphasis is put on illustrating how dual doping regulates the external and internal properties and boosts the catalytic performance of catalysts. Additionally, perspectives are pointed out to guide future research on engineering high‐performance heteroatom‐doped electrocatalysts.

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http://hdl.handle.net/10453/186363