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Journal of materials chemistry. A, Materials for energy and sustainability, 2021-08, Vol.9 (31), p.16917-16927
2021
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Autor(en) / Beteiligte
Titel
An EPR investigation of defect structure and electron transfer mechanism in mixed-conductive LiBO2–V2O5 glasses
Ist Teil von
  • Journal of materials chemistry. A, Materials for energy and sustainability, 2021-08, Vol.9 (31), p.16917-16927
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2021
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Continuous Wave (CW) Electron Paramagnetic Resonance (EPR) spectroscopy was used to study the defect structure and electron transfer mechanism in a series of LiBO2–V2O5 mixed conductive glasses of varying V2O5 content. These glassy materials are attracting growing interest for energy storage devices. At low V2O5 content (VLB1), an isolated S = ½ vanadium defect centre is found at a network modifying position within the LiBO2 matrix. The observed spin Hamiltonian parameters are consistent with a V4+ centre possessing a distorted octahedral configuration and dxy orbital ground state. At high V2O5 content (VLB3), the vanadium hyperfine structure is absent indicative of a distinct exchange-narrowed signal. A model was developed to analyse the linewidth and g-tensor component of the EPR signals, revealing a marked temperature dependent behaviour, consistent with a polaron hopping mechanism of electron transfer and inter-electronic exchange along the g3 direction, coincident with the electron transfer axis. The activation energy (Ea) was estimated to be 0.081 eV, consistent with other conducting glasses. A relaxation-dominated line broadening mechanism was further supported by multi-frequency EPR measurements, which also identified unresolved features at high frequencies due to unaccounted for anisotropic exchange/speciation within the disordered network. This analysis provides a straight-forward method for the use of EPR to investigate solid-state glassy materials.
Sprache
Englisch
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/d1ta02352g
Titel-ID: cdi_proquest_journals_2559642646

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