4.6 Article

Manipulating Interfacial Dissolution-Redeposition Dynamics to Resynthesize Electrode Surface Chemistry

期刊

ACS ENERGY LETTERS
卷 7, 期 8, 页码 2588-2594

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.2c01186

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资金

  1. National Science Foundation [CBET 1912876, CBET 1912885]
  2. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-76SF00515]
  3. Walter Ahlstrom Foundation
  4. European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie Grant [841621]
  5. DOE Office of Science [DE-AC02-06CH11357]
  6. U.S. Department of Energy Office of Science User Facility, at Brookhaven National Laboratory [DE-SC0012704]
  7. Virginia Tech's Institute for Critical Technology and Applied Science
  8. Marie Curie Actions (MSCA) [841621] Funding Source: Marie Curie Actions (MSCA)

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This study investigates the reactive environment of the solid-liquid electrochemical interface and demonstrates that the dissolution and redeposition kinetics of transition metal cations can be manipulated to regulate the chemical composition and crystal structure of the electrode surface, as well as the overall electrochemical performance.
The solid-liquid electrochemical interface offers a reactive environment for interfacial reactions to tailor electrode surface chemistry under operating conditions. Herein, we demonstrate that the dissolution and redeposition kinetics of transition metal cations, a ubiquitous phenomenon at the electrochemical interface, can be manipulated to regulate the chemical composition and crystal structure of the electrode surface, as well as the overall electrochemical performance. Foreign cations (e.g., Ti4+) either added as electrolyte additives or dissolved from surface coatings, can rapidly participate in the electrode dissolution-redeposition process and facilitate the establishment of the dissolution-redeposition equilibrium. Our work expands the control over the electrochemical reactions at the solid-liquid interface and provides new insights into interfacial studies in electrochemistry and surface science.

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