TY - JOUR
T1 - Molecular Nature of Electrodeposits in Electrochemical Water Oxidation
AU - Younus, Hussein A.
AU - Ahmad, Nazir
AU - Al-Abri, Mohammed
AU - Al-Hajri, Rashid
AU - Zhang, Shiguo
N1 - Funding Information:
This work was financially supported by the Intergovernmental International Science and Technology Innovation Cooperation Program of National Key Research and Development Program (Grant No. 2022YFE0120200), the Egyptian Science and Develoment Fund (STDF) (Grant No. 44288), the National Natural Science Foundation of China (Grant Nos. 21872046, 52072118, and 52102041), and the Jiebang Guashuai Project of Hunan Province (Grant No. 2021GK1230). The authors would like to express their gratitude to Prof. A. Llobet for taking the time to review and provide valuable feedback on this manuscript.
Publisher Copyright:
© 2023 Wiley-VCH GmbH.
PY - 2023/7/7
Y1 - 2023/7/7
N2 - The molecular nature and the structure of the real catalyst are matters of serious concern in homogeneous catalysis. Catalyst transformation in molecular water oxidation catalysis (WOC) is usually linked to catalyst decomposition with the generation of nanostructured materials. This is mainly due to the operational conditions that are conducive for the formation of metal oxides (MOx), which have a strong affinity for adsorbing onto the electrodes’ surfaces. Recently, the exhibition of the molecular nature of the electrodeposits rather than MOx is a breakthrough in the field of WOC, suggesting that deposits in electrocatalysis are not constrained to metal oxides/hydroxides after molecular catalyst decomposition. Therefore, several points should be considered before deciding whether the deposits are aggregates of a molecular structure or simple metal oxides formed due to the decomposition of the original structure. Thus, the aim of this perspective is to showcase the examples of homogeneous WOCs where metal–organic species are electrodeposited instead of metal oxide-based catalysts. The transformation of heterogenized molecular catalysts for WO into a more electroactive form while preserving their molecular identity, is also discussed. This summary provides an overview of the molecular nature of electrodeposits, how to identify their presence and decide about their nature.
AB - The molecular nature and the structure of the real catalyst are matters of serious concern in homogeneous catalysis. Catalyst transformation in molecular water oxidation catalysis (WOC) is usually linked to catalyst decomposition with the generation of nanostructured materials. This is mainly due to the operational conditions that are conducive for the formation of metal oxides (MOx), which have a strong affinity for adsorbing onto the electrodes’ surfaces. Recently, the exhibition of the molecular nature of the electrodeposits rather than MOx is a breakthrough in the field of WOC, suggesting that deposits in electrocatalysis are not constrained to metal oxides/hydroxides after molecular catalyst decomposition. Therefore, several points should be considered before deciding whether the deposits are aggregates of a molecular structure or simple metal oxides formed due to the decomposition of the original structure. Thus, the aim of this perspective is to showcase the examples of homogeneous WOCs where metal–organic species are electrodeposited instead of metal oxide-based catalysts. The transformation of heterogenized molecular catalysts for WO into a more electroactive form while preserving their molecular identity, is also discussed. This summary provides an overview of the molecular nature of electrodeposits, how to identify their presence and decide about their nature.
KW - metal–organic films
KW - molecular catalysis
KW - molecular electrodeposits
KW - oxygen evolution reaction
KW - true catalyst
KW - water oxidation
UR - http://www.scopus.com/inward/record.url?scp=85159723318&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85159723318&partnerID=8YFLogxK
U2 - 10.1002/aenm.202300896
DO - 10.1002/aenm.202300896
M3 - Article
AN - SCOPUS:85159723318
SN - 1614-6832
VL - 13
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 25
M1 - 2300896
ER -