Facet-engineered ruthenium oxide on titanium oxide oxygen evolution electrocatalysts for proton-exchange membrane water electrolysis

被引:0
|
作者
Yoon, Hyunseok [1 ]
Song, Hee Jo [2 ]
Hyoung, Ji Seong [1 ]
Jung, Sang Won [3 ]
Haryanto, Andi [4 ]
Lee, Chan Woo [4 ]
Kim, Dong-Wan [1 ,3 ]
机构
[1] School of Civil, Environmental and Architectural Engineering, Korea University, Seoul,02841, Korea, Republic of
[2] Department of Nanotechnology and Advanced Materials Engineering, Sejong University, Seoul,05006, Korea, Republic of
[3] KU-LG Energy Solution Department of Battery-Smart Factory, Korea University, Seoul,02841, Korea, Republic of
[4] Department of Chemistry, Kookmin University, Seoul,02707, Korea, Republic of
基金
新加坡国家研究基金会;
关键词
Crystal orientation - Density functional theory - Electrolysis - Electrolytic cells - Interface states - Morphology - Oxide minerals - Oxygen - Proton exchange membrane fuel cells (PEMFC) - Ruthenium compounds - Titanium dioxide;
D O I
10.1016/j.apcatb.2024.124382
中图分类号
学科分类号
摘要
Ruthenium oxide-based catalysts exhibit an active oxygen evolution reaction (OER) in acidic media but suffer from low stability, limiting their practical application in proton-exchange membrane water electrolyzers (PEMWEs). Herein, we present an effective acidic OER catalyst comprising RuO2 nanolayers on an isostructural rutile TiO2 support (NL-RuO2-250) that maximizes exposure to specific crystal orientations. RuO2 morphology and growth mechanism on the TiO2 surface were affected by the interfacial charge states during hydrothermal process, with the crystal structure similarity between the RuO2 catalyst and TiO2 support advantageous for maximizing compatibility at the interface. Density functional theory combined with experimental analyses revealed that NL-RuO2-250 is an optimized form for improving OER performance. As-prepared NL-RuO2-250 required a low overpotential (230 mV at 10 mA cm−2) and a PEMWE single cell assembled with NL-RuO2-250 exhibited an insignificant voltage drop for 24 h under 0.2 A cm−2, demonstrating a practical design strategy for acidic OER catalysts. © 2024 Elsevier B.V.
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