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

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. % Ni<sub>2</sub>FeCo doping in Mo<sub>2</sub>C, significantly surpassing the thermodynamic equilibrium limit of <3 at. %. The supersaturation ensures more catalytically active NiFeCo doping and sufficient interaction with Mo<sub>2</sub>C, 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<sup>-2</sup> and stable for 700 h, while individual Ni<sub>2</sub>FeCo and Mo<sub>2</sub>C only last less than 70 and 10 h (completely dissolved), respectively. In particular, the SD-Mo<sub>2</sub>C catalyst also exhibits excellent durability at 100 mA cm<sup>-2</sup> 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 Mo<sub>2</sub>C 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 cm<sup>2</sup>) 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 Ni<sub>2</sub>FeCo-doped TiC, NbC, and W<sub>2</sub>C, thus unlocking the potential of maximized or adjustable MSI for diverse catalytic applications.

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Publication Details

Journal
ACS Nano
Published
2024-10-14
DOI
https://doi.org/10.1021/acsnano.4c09249
Citations
25
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
2.56

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article

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

Wenhui Shi, Yifei Yuan, Bao Yu Xia, Anmin Nie et al.
25 citations
ACS Nano
Electrocatalysts for Energy Conversion
2.56
article

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

Wenhui Shi, Yifei Yuan, Bao Yu Xia, Anmin Nie, Yunjie Mei, Qi Wang, Jinli Chen, Yonggang Yao, Yi Rao, Yaqing Guo, Hanwen Liu, Lin Cheng, Shijing Liu
article en
25 citations

Abstract

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. % Ni<sub>2</sub>FeCo doping in Mo<sub>2</sub>C, significantly surpassing the thermodynamic equilibrium limit of <3 at. %. The supersaturation ensures more catalytically active NiFeCo doping and sufficient interaction with Mo<sub>2</sub>C, 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<sup>-2</sup> and stable for 700 h, while individual Ni<sub>2</sub>FeCo and Mo<sub>2</sub>C only last less than 70 and 10 h (completely dissolved), respectively. In particular, the SD-Mo<sub>2</sub>C catalyst also exhibits excellent durability at 100 mA cm<sup>-2</sup> 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 Mo<sub>2</sub>C 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 cm<sup>2</sup>) 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 Ni<sub>2</sub>FeCo-doped TiC, NbC, and W<sub>2</sub>C, thus unlocking the potential of maximized or adjustable MSI for diverse catalytic applications.

ACS NanoVol. 18(43)
Wenzhou University (CN), Yanshan University (CN), Ministry of Education (RO), Division of Materials Science and Engineering (AU), Science and Technology on Surface Physics and Chemistry Laboratory (CN), Center for High Pressure Science and Technology Advanced Research (CN), State Key Laboratory of Materials Processing and Die & Mould Technology (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, Huazhong University of Science and Technology, Shenzhen International Cooperation Research Project, National Key Research and Development Program of China
Openalex Percentile: Top 10%
Electrocatalysts for Energy Conversion
2.56
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