Affiliation:
1. Institute of Functional Nano and Soft Materials (FUNSOM) Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices Soochow University 215123 Suzhou P. R. China
2. Department of Chemistry: Metalorganics and Inorganic Materials Technische Universität Berlin Straße des 17 Juni 135, Sekr. C2 10623 Berlin Germany
3. Materials Chemistry Group for Thin Film Catalysis – CatLab Helmholtz-Zentrum Berlin für Materialien und Energie Albert-Einstein-Str. 15 12489 Berlin Germany
Abstract
AbstractDespite being considered as efficient non‐noble metal‐based electrocatalysts for alkaline oxygen evolution reaction (OER), NiFe (oxy)hydroxides (NiFeOxHy) typically fall short of meeting practical requirements. To address this challenge, herein, we introduce a facile in situ electrochemical incorporation technique to form Sn‐doped NiFe‐layered double hydroxide (NiFeSn‐LDH) precatalysts. Subsequently, under the alkaline OER process, the precatalyst evolves into stannate ion‐adsorbed NiFe oxyhydroxides (NiFeOOH). The presence of these stable stannate oxyanions plays a key role in mitigating Fe leaching, optimizing the electronic structure of NiFeOOH, and improving its reaction kinetics, thereby significantly enhancing alkaline OER performance. Notably, the nickel foam‐supported NiFeSn‐LDH demonstrates impressive results delivering a large current density of 100 mA cm−2 at an overpotential as low as ~260 mV and maintaining the industrial‐relevant ~500 mA cm−2 current density over 5 days with negligible activity decay, surpassing the performances of most of the transition metal‐based electrocatalysts. Comprehensive advanced characterizations of the precatalysts, before and after the OER reactions, have been performed to uncover stable residual stannate ions at the surface of NiFeOxHy and to determine their pivotal role in promoting alkaline OER.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Jiangsu Province
Cited by
1 articles.
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