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Designing Supported Nanoparticles via Synergistic Ex-Solution and Phosphorization for Tailored Active Site Generationopen access

Authors
Kim, Jun KyuKim, SangwooKim, Yong BeomKoo, BonjaeOh, DonghwanKim, HyunseungKim, KyeounghakHan, Jeong WooJung, Woochul
Issue Date
Jul-2025
Publisher
WILEY-V C H VERLAG GMBH
Keywords
ex-solution; heterogeneous catalysts; hydrogen evolution reaction; metal phosphide
Citation
ADVANCED MATERIALS, v.37, no.26, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
ADVANCED MATERIALS
Volume
37
Number
26
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211616
DOI
10.1002/adma.202417576
ISSN
0935-9648
1521-4095
Abstract
Supported nanoparticles incorporating catalytically attractive nonmetal elements have gained significant attention as a promising strategy for enhancing catalytic activity in various industrial applications. This study presents an innovative one-pot synthesis method for fabricating hybrid catalysts, which simultaneously modifies surface properties through the precipitation of nanoparticles with the concurrent incorporation of nonmetal elements. The underlying concept is to synchronize the temperature required for particle formation with that of nonmetal incorporation by adjusting the oxygen chemical potential of the host oxide. As a case study, Ir- and Ru-doped WO3 are selected as the starting material, with phosphorus (P) as the representative nonmetal for surface functionalization. Notably, the hybrid catalyst, composed of amorphous (Ir,Ru)Px particles dispersed on P-rich WO2.9 sheets, is synthesized through a single heat treatment at 500 °C, avoiding undesirable sintering of the host material. When used as a hydrogen evolution catalyst, this material exhibits outstanding mass activity, durability, compared to state-of-the-art Pt/C catalysts. Density functional theory calculations further reveal that the superior performance of the hybrid catalysts attributes to improved water dissociation and favorable adsorption and desorption of key reaction intermediates. This novel synthesis strategy offers considerable potential for advancing diverse areas of heterogeneous catalysis.
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