Journal article
Ordered-vacancy-induced cation intercalation into layered double hydroxides: A general approach for high-performance supercapacitors
- Abstract:
- New types of cation storage materials would show tremendous potential in the development of high-performance rechargeable energy storage devices. Herein, we develop layered double hydroxides (LDHs) as promising cation supercapacitor materials in aqueous and neutral operation, via an effective electrochemical activation strategy, for a reversible intercalation of a wide range of metal cations. These activated LDH materials exhibit overwhelming metal-ion storage capacities in aqueous electrolytes as a result of the phase transformation of LDH (repulsive to cations) to hydrogen-vacancy-enriched LDH (LDH-HV, attractive to cations) induced by the electrochemical activation process. The activated LDH-HV phase provides a two-dimensional open channel with abundant active sites (HV) for a reversible intercalation of metal ions, accounting for the significantly enhanced energy storage performance. This vacancy-induced cation intercalation into LDHs builds up a general approach for developing earth-abundant transition-metal resources as a prospective energy storage material toward a large variety of cation supercapacitors.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 2.2MB, Terms of use)
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- Publisher copy:
- 10.1016/j.chempr.2018.06.007
Authors
- Publisher:
- Cell Press
- Journal:
- Chem More from this journal
- Volume:
- 4
- Issue:
- 9
- Pages:
- 2168-2179
- Publication date:
- 2018-07-05
- Acceptance date:
- 2018-06-15
- DOI:
- EISSN:
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2451-9294
- Keywords:
- Pubs id:
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pubs:867548
- UUID:
-
uuid:c645d0ea-88a2-4444-bc22-458a49b0cd01
- Local pid:
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pubs:867548
- Source identifiers:
-
867548
- Deposit date:
-
2018-10-29
- ARK identifier:
Terms of use
- Copyright holder:
- Elsevier Inc
- Copyright date:
- 2018
- Notes:
- Copyright © 2018 Elsevier Inc. This is the accepted manuscript version of the article. The final version is available online from Cell Press at: https://doi.org/10.1016/j.chempr.2018.06.007
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