A highly active and stable 3D dandelion spore-structured self-supporting Ir-based electrocatalyst for proton exchange membrane water electrolysis fabricated using structural reconstruction

被引:0
作者
Yeo, Kyeong-Rim [1 ]
Lee, Kug-Seung [2 ]
Kim, Hoyoung [3 ]
Lee, Jinwoo [3 ]
Kim, Soo-Kil [1 ]
机构
[1] School of Integrative Engineering, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul,06974, Korea, Republic of
[2] Pohang Accelerator Laboratory, 80 Jigok-ro, Nam-gu, Pohang,37673, Korea, Republic of
[3] Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon,34141, Korea, Republic of
基金
新加坡国家研究基金会;
关键词
Binary alloys - Corrosion resistance - Dealloying - Degradation - Electrolysis - Electrolytes - Energy efficiency - Fabrication - Image reconstruction - Stability - Temperature - Ternary alloys;
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摘要
Proton exchange membrane water electrolysis (PEMWE), the most energy-efficient low-temperature electrolysis method, is promising for converting intermittent renewable energies into stable hydrogen chemical energy. However, the cumulative corrosive environment resulting from the acidic conditions required and the positive half-cell potentials imply that only materials having high intrinsic activity and stability can be used. Herein, we propose catalysts and a corresponding fabrication method that meets these requirements. A 3D dandelion spore-structured self-supporting IrNi electrocatalyst is directly fabricated on a porous transport layer through the adsorbed H-induced co-electrodeposition of a core-shell IrNi-Ir structure. Subsequent dealloying generates a highly porous nanostructured Ir-based framework robust to the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in a wide pH range. Specifically, it exhibited overpotentials of 248 mV (OER) and 15 mV (HER) at ±10 mA cm−2 in an acidic electrolyte with exceptional stability even after constant operation at 200 mA cm−2 for 50 h (OER) or 5000 potential cycles (HER). When used as a bifunctional catalyst (0.67 mg cm−2) for PEMWE, 6.5 A cm−2 was obtained at a cell voltage of 2.0 V. The degradation rate was only 1.58 mV h−1 under extremely harsh test conditions of 2 A cm−2 for 100 h, thus verifying the exceptional stability of a single cell. This is the first report of bifunctional catalysts with such high performance and stability fabricated using a simple method, and this work can aid the commercialization of PEMWE. © 2022 The Royal Society of Chemistry.
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页码:3449 / 3461
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