4.8 Article

Morphology Dynamics of Single-Layered Ni(OH)2/NiOOH Nanosheets and Subsequent Fe Incorporation Studied by &ITin Situ&IT Electrochemical Atomic Force Microscopy

期刊

NANO LETTERS
卷 17, 期 11, 页码 6922-6926

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.7b03313

关键词

Ni(OH)(2); EC-AFM; supercapacitor; oxygen evolution reaction; Fe incorporation

资金

  1. Zhejiang University
  2. National Key R&D Program of China [2016YFA0202900]
  3. National Natural Science Foundation of China [21622308]
  4. NSF Major Research Instrumentation Program [DMR-1532225]
  5. W. M. Keck Foundation
  6. M. J. Murdock Charitable Trust
  7. ONAMI
  8. Air Force Research Laboratory
  9. National Science Foundation
  10. University of Oregon
  11. National Science Foundation Chemical Catalysis program [CHE-1566348]
  12. Direct For Mathematical & Physical Scien
  13. Division Of Chemistry [1566348] Funding Source: National Science Foundation
  14. Direct For Mathematical & Physical Scien
  15. Division Of Materials Research [1532225] Funding Source: National Science Foundation

向作者/读者索取更多资源

Nickel (oxy)hydroxide-based (NiOxHy) materials are widely used for energy storage and conversion devices. Understanding dynamic processes at the solid-liquid interface of nickel (oxy)hydroxide is important to improve reaction kinetics and efficiencies. In this study, in situ electrochemical atomic force microscopy (EC-AFM) was used to directly investigate dynamic changes of single-layered Ni(OH)(2) nanosheets during electrochemistry measurements. Reconstruction of Ni(OH)(2) nanosheets, along with insertion of ions from the electrolyte, results in an increase of the volume by 56% and redox capacity by 300%. We also directly observe Fe cations adsorb and integrate heterogeneously into or onto the nanosheets as a function of applied potential, further increasing apparent volume. Our findings are important for the fundamental understanding of NiOxHy-based supercapacitors and oxygen-evolution catalysts, illustrating the dynamic nature of Ni-based nanostructures under electrochemical conditions.

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