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Nanosized Chevrel phases for dendrite-free zinc-ion based energy storage: unraveling the phase transformations.
Elgendy, Amr; Papaderakis, Athanasios A; Ejigu, Andinet; Helmbrecht, Katharina; Spencer, Ben F; Groß, Axel; Walton, Alex S; Lewis, David J; Dryfe, Robert A W.
Affiliation
  • Elgendy A; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK. robert.dryfe@manchester.ac.uk.
  • Papaderakis AA; Henry Royce Institute, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Ejigu A; Egyptian Petroleum Research Institute, 11727, Cairo, Egypt.
  • Helmbrecht K; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK. robert.dryfe@manchester.ac.uk.
  • Spencer BF; Henry Royce Institute, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Groß A; Department of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL, UK. robert.dryfe@manchester.ac.uk.
  • Walton AS; Henry Royce Institute, University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
  • Lewis DJ; Institute of Theoretical Chemistry, Ulm University, Albert-Einstein-Allee 11, 89081 Ulm, Germany.
  • Dryfe RAW; Helmholtz Institute Ulm (HIU) for Electrochemical Energy Storage, Helmholtzstraße 11, 89081 Ulm, Germany.
Nanoscale ; 16(28): 13597-13612, 2024 Jul 18.
Article de En | MEDLINE | ID: mdl-38958552
ABSTRACT
The nanoscale form of the Chevrel phase, Mo6S8, is demonstrated to be a highly efficient zinc-free anode in aqueous zinc ion hybrid supercapacitors (ZIHSCs). The unique morphological characteristics of the material when its dimensions approach the nanoscale result in fast zinc intercalation kinetics that surpass the ion transport rate reported for some of the most promising materials, such as TiS2 and TiSe2. In situ Raman spectroscopy, post-mortem X-ray diffraction, Hard X-ray photoelectron spectroscopy, and density functional theory (DFT) calculations were combined to understand the overall mechanism of the zinc ion (de)intercalation process. The previously unknown formation of the sulfur-deficient Zn2.9Mo15S19 (Zn1.6Mo6S7.6) phase is identified, leading to a re-evaluation of the mechanism of the (de)intercalation process. A full cell comprised of an activated carbon (YEC-8A) positive electrode delivers a cell capacity of 38 mA h g-1 and an energy density of 43.8 W h kg-1 at a specific current density of 0.2 A g-1. The excellent cycling stability of the device is demonstrated for up to 8000 cycles at 3 A g-1 with a coulombic efficiency close to 100%. Post-mortem microscopic studies reveal the absence of dendrite formation at the nanosized Mo6S8 anode, in stark contrast to the state-of-the-art zinc electrode.

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nanoscale Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nanoscale Année: 2024 Type de document: Article Pays d'affiliation: Royaume-Uni