Direct Synthesis of Dual Mo-Based Functional Materials Derived from Molybdenite by Molten Salt Paired Electrolysis

A facile synthesis process that facilitates the industrial-scale production of catalysts is the prerequisite of the hydrogen evolution reaction (HER) industry. Molybdenum-based catalysts are ideal alternatives for precious-metal-based HER materials; however, they remain challenging in scale-up preparation due to the costly and complex Mo sources. Herein, we propose a molten salt paired electrolysis approach to synthesize transition-metal-doped Mo<sub>2</sub>C catalysts directly from molybdenite (mainly consisting of micrometer-scale MoS<sub>2</sub> bulks), an earth-abundant natural Mo ore. Unlike Fe-doped Mo<sub>2</sub>C in which those transition metal dopants are inclined to diffuse into inner planes of Mo<sub>2</sub>C, this unique synthesis approach leverages the differences in transition metal diffusion energy barriers, ultimately leading to the development of Ni-doped Mo<sub>2</sub>C catalytic materials with specific Ni-enriched interfaces. Owing to the unique design and structures of the catalyst, the interfacially Ni-enriched Ni-doped Mo<sub>2</sub>C exhibited promising HER performance and long-term stability. Very interestingly, MoS<sub>2</sub> nanoflakes, as side products, can be collected at the anode side while interfacially Ni-enriched Mo<sub>2</sub>C was concurrently obtained at the cathode side during the electrolytic synthesis process. This work not only deepens our knowledge on constructing active-site-enriched interfaces that are beneficial to HER but also gives clues to upcycling raw materials.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2025-03-28
DOI
https://doi.org/10.1021/acsami.4c19822
Citations
1
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
0.36

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article

Direct Synthesis of Dual Mo-Based Functional Materials Derived from Molybdenite by Molten Salt Paired Electrolysis

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1 citations
ACS Applied Materials & Interfaces
Electrocatalysts for Energy Conversion
0.36
article

Direct Synthesis of Dual Mo-Based Functional Materials Derived from Molybdenite by Molten Salt Paired Electrolysis

Dihua Wang, Liangyou Hu, Rui Jiang, Yanwei Wen, Pi Liu, Bowen Deng, Xuhui Mao, Huijun Liu, Xinyu Li, Wen Lei
article en
1 citations

Abstract

A facile synthesis process that facilitates the industrial-scale production of catalysts is the prerequisite of the hydrogen evolution reaction (HER) industry. Molybdenum-based catalysts are ideal alternatives for precious-metal-based HER materials; however, they remain challenging in scale-up preparation due to the costly and complex Mo sources. Herein, we propose a molten salt paired electrolysis approach to synthesize transition-metal-doped Mo<sub>2</sub>C catalysts directly from molybdenite (mainly consisting of micrometer-scale MoS<sub>2</sub> bulks), an earth-abundant natural Mo ore. Unlike Fe-doped Mo<sub>2</sub>C in which those transition metal dopants are inclined to diffuse into inner planes of Mo<sub>2</sub>C, this unique synthesis approach leverages the differences in transition metal diffusion energy barriers, ultimately leading to the development of Ni-doped Mo<sub>2</sub>C catalytic materials with specific Ni-enriched interfaces. Owing to the unique design and structures of the catalyst, the interfacially Ni-enriched Ni-doped Mo<sub>2</sub>C exhibited promising HER performance and long-term stability. Very interestingly, MoS<sub>2</sub> nanoflakes, as side products, can be collected at the anode side while interfacially Ni-enriched Mo<sub>2</sub>C was concurrently obtained at the cathode side during the electrolytic synthesis process. This work not only deepens our knowledge on constructing active-site-enriched interfaces that are beneficial to HER but also gives clues to upcycling raw materials.

ACS Applied Materials & InterfacesVol. 17(14)
Wuhan University (CN), China International Science and Technology Cooperation (CN)
National Natural Science Foundation of China
Affordable and clean energy
Openalex Percentile: Top 45%
Electrocatalysts for Energy Conversion
0.36
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