IrO2 Nanoparticle-Decorated Ir-Doped W18O49 Nanowires with High Mass Specific OER Activity for Proton Exchange Membrane Electrolysis

被引:35
|
作者
Yan, Tianqing [1 ,2 ,3 ]
Chen, Shiyi [1 ,2 ,3 ]
Sun, Wendi [1 ]
Liu, Yuezheng [1 ]
Pan, Lun [1 ,2 ,3 ]
Shi, Chengxiang [1 ,2 ,3 ]
Zhang, Xiangwen [1 ,2 ,4 ]
Huang, Zhen-Feng [1 ,2 ,3 ]
Zou, Ji-Jun [1 ,2 ,3 ,4 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Key Lab Green Chem Technol Minist Educ, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Tianjin Univ, Zhejiang Inst, Tianjin 315201, Peoples R China
[4] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
PEM water electrolysis; oxygen evolution reaction; structure-activity relation; iridium; OXYGEN EVOLUTION REACTION; TIO2; NANOTUBES; SUPPORT; ELECTROCATALYST; CATALYSTS; OXIDATION; STORAGE; OXIDES;
D O I
10.1021/acsami.2c20529
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The oxygen evolution reaction (OER) severely limits the efficiency of proton exchange membrane (PEM) electrolyzers due to slow reaction kinetics. IrO2 is currently a commonly used anode catalyst, but its large-scale application is limited due to its high price and scarce reserves. Herein, we reported a practical strategy to construct an acid OER catalyst where Iridium oxide loading and iridium element bulk doping are realized on the surface and inside of W18O49 nanowires by immersion adsorption, respectively. Specifically, W0.7Ir0.3Oy has an overpotential of 278 mV at 10 mA center dot cm-2 in 0.1 M HClO4. The mass activity of 714.10 A center dot gIr-1 at 1.53 V vs. the reversible hydrogen electrode (RHE) is 80 times that of IrO2, and it can run stably for 55 h. In the PEM water electrolyzer device, its mass activity reaches 3563.63 A center dot gIr-1 at the cell voltage of 2.0 V. This improved catalytic performance is attributed to the following aspects: (1) The electron transport between iridium and tungsten effectively improves the electronic structure of the catalyst; (2) the introduction of iridium into W18O49 by means of elemental bulk doping and nanoparticles supporting for the enhanced conductivity and electrochemically active surface area of the catalyst, resulting in extensive exposure of active sites and increased intrinsic activity; and (3) during the OER process, partial iridium elements in the bulk phase are precipitated, and iridium oxide is formed on the surface to maintain stable activity. This work provides a new idea for designing oxygen evolution catalysts with low iridium content for practical application in PEM electrolyzers.
引用
收藏
页码:6912 / 6922
页数:11
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