4.8 Article

2D High-Entropy Transition Metal Dichalcogenides for Carbon Dioxide Electrocatalysis

Journal

ADVANCED MATERIALS
Volume 33, Issue 31, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202100347

Keywords

2D materials; electrocatalysis; high entropy alloys; transition metal dichalcogenides

Funding

  1. National Science Foundation (NSF) [DMREF 1729420]
  2. NSF-CBET [1800357]
  3. NSF CBET [1729787]
  4. NSF [DMR-1806147, DMR-1809571, ACI-1548562]
  5. Office of Nuclear Energy, Fuel Cycle RD Program
  6. Nuclear Science User Facilities
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [1800357] Funding Source: National Science Foundation
  9. Div Of Chem, Bioeng, Env, & Transp Sys
  10. Directorate For Engineering [1729787] Funding Source: National Science Foundation

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The research reports the prediction, synthesis, and multiscale characterization of 2D high-entropy transition metal dichalcogenide alloys with four/five transition metals, with MoWVNbTaS-2 alloy showing excellent electrochemical performance in CO2 conversion to CO. First-principles calculations demonstrate that the superior CO2 electroreduction is due to multi-site catalysis optimizing the rate-limiting step of CO desorption.
High-entropy alloys combine multiple principal elements at a near equal fraction to form vast compositional spaces to achieve outstanding functionalities that are absent in alloys with one or two principal elements. Here, the prediction, synthesis, and multiscale characterization of 2D high-entropy transition metal dichalcogenide (TMDC) alloys with four/five transition metals is reported. Of these, the electrochemical performance of a five-component alloy with the highest configurational entropy, (MoWVNbTa)S-2, is investigated for CO2 conversion to CO, revealing an excellent current density of 0.51 A cm(-2) and a turnover frequency of 58.3 s(-1) at approximate to -0.8 V versus reversible hydrogen electrode. First-principles calculations show that the superior CO2 electroreduction is due to a multi-site catalysis wherein the atomic-scale disorder optimizes the rate-limiting step of CO desorption by facilitating isolated transition metal edge sites with weak CO binding. 2D high-entropy TMDC alloys provide a materials platform to design superior catalysts for many electrochemical systems.

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