Metal-Support Interaction Can Deactivate IrOx/Sb:SnO2 OER Catalysts in Polyol Process

被引:20
作者
Jang, Hansaem [1 ]
Lee, Jeong-Hyeon [1 ]
Lee, Jeon Ryang [1 ]
Kim, Tae-Won [1 ]
机构
[1] Korea Inst Ind Technol KITECH, Green Energy & Nano Technol R&D Grp, Gwangju 61012, South Korea
关键词
antimony tin oxide; electrocatalyst; electrolysis; iridium oxide; microwave irradiation; nanoparticle; water oxidation; water splitting; OXYGEN EVOLUTION REACTION; HIGH-PERFORMANCE; IRIDIUM OXIDE; STABILITY; NANOPARTICLES; IRRADIATION;
D O I
10.1021/acsaem.2c01765
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Only a few materials can remain undissolved under working conditions for the oxygen evolution reaction (OER) in acidic media, which limits the choice of catalysts and supports. One of the practical catalyst/support candidates is IrOx/Sb:SnO2 (Ir/ATO) because both components are thermodynamically stable under low-pH anodic conditions. Moreover, between Ir and ATO, a strong metal- support interaction is present, thereby allowing for long-lasting OER activity unless the support degrades. However, we demonstrate that the strong interaction can paradoxically deactivate Ir/ATO structures when synthesizing them using the polyol process. We reveal that the strong interaction in the presence of polyol at elevated temperatures can cause the reduction of the Sb dopant to zero-valency. Findings show that the varied oxidation state of the dopant decreases the electrical conductivity of the Ir/ATO, impeding the electron transfer through the support, hence deteriorating electrocatalytic activity toward the OER.
引用
收藏
页码:9297 / 9302
页数:6
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