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Supersaturated Doping-Induced Maximized Metal–Support Interaction for Highly Active and Durable Oxygen Evolution

材料科学 兴奋剂 析氧 氧气 过饱和度 金属 化学工程 纳米技术 化学 冶金 电极 光电子学 工程类 有机化学 物理化学 电化学
作者
Hanwen Liu,Wenhui Shi,Yaqing Guo,Yunjie Mei,Yi Rao,Jinli Chen,Shiyuan Liu,Lin Cheng,Anmin Nie,Qi Wang,Yifei Yuan,Bao Yu Xia,Yonggang Yao
出处
期刊:ACS Nano [American Chemical Society]
卷期号:18 (43): 29724-29735 被引量:8
标识
DOI:10.1021/acsnano.4c09249
摘要

Metal–support interaction (MSI) is pivotal and ubiquitously used in the development of next-generation catalysts, offering a pathway to enhance both catalytic activity and stability. However, owing to the lattice mismatch and poor solubility, traditional catalysts often exhibit a metal-on-support heterogeneous structure with limited interfaces and interaction and, consequently, a compromised enhancement of properties. Herein, we report a universal and tunable method for supersaturated doping of transition-metal carbides via strongly nonequilibrium carbothermal shock synthesis, characterized by rapid heating and swift quenching. Our results enable ∼20 at. % Ni2FeCo doping in Mo2C, significantly surpassing the thermodynamic equilibrium limit of <3 at. %. The supersaturation ensures more catalytically active NiFeCo doping and sufficient interaction with Mo2C, resulting in the maximized MSI (Max-MSI) effect. The Max-MSI enables outstanding activity and particularly stability in alkaline oxygen evolution reaction, showing an overpotential of 284 mV at 100 mA cm–2 and stable for 700 h, while individual Ni2FeCo and Mo2C only last less than 70 and 10 h (completely dissolved), respectively. In particular, the SD-Mo2C catalyst also exhibits excellent durability at 100 mA cm–2 for up to 400 h in 7 M KOH. Such a significantly improved stability is attributed to the supersaturated doping that led to each Mo atom strongly binding with adjacent heteroatoms, thus elevating the dissolution potential and corrosion resistance of Mo2C at a high current density. Additionally, the highly dispersed NiFeCo also facilitates the formation of dense oxyhydroxide coating during reconstruction, further protecting the integrated catalysts for durable operation. Furthermore, the synthesis has been successfully scaled up to fabricate large (16 cm2) electrodes and is adaptable to nickel foam substrates, indicating promising industrial applications. Our strategy allows the general and versatile production of various highly doped transition-metal carbides, such as Ni2FeCo-doped TiC, NbC, and W2C, thus unlocking the potential of maximized or adjustable MSI for diverse catalytic applications.
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