Redox-active benzoquinone-intercalated layered vanadate for high performance zinc-ion battery: Phenol-keto conversion and the anchoring effect of V-O-V host framework

•(o-BQ)0.25V2O5·0·5H2O and (p-BQ)0.25V2O5·0·5H2O (BQ = benzoquinone) were synthesized.•Rietveld refinements and HAADF-STEM reveal the successful intercalation of BQ into V2O5.•(p-BQ)0.25V2O5·0·5H2O shows an excellent rate performance and an ultralong cycle life.•The sandwiched BQ in layered V2O5 can...

Full description

Saved in:
Bibliographic Details
Published inElectrochimica acta Vol. 436; p. 141447
Main Authors Liu, Chang Lin, Cao, Tong, Wang, Zhao Peng, Li, Kai, Gong, Yun, Zhang, Da Liang
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 20.12.2022
Subjects
Online AccessGet full text
ISSN0013-4686
1873-3859
DOI10.1016/j.electacta.2022.141447

Cover

More Information
Summary:•(o-BQ)0.25V2O5·0·5H2O and (p-BQ)0.25V2O5·0·5H2O (BQ = benzoquinone) were synthesized.•Rietveld refinements and HAADF-STEM reveal the successful intercalation of BQ into V2O5.•(p-BQ)0.25V2O5·0·5H2O shows an excellent rate performance and an ultralong cycle life.•The sandwiched BQ in layered V2O5 can be prevented from leaching into the electrolyte.•DFT calculations disclose a small Zn2+-migration barrier in (p-BQ)0.25V2O5·xH2O. Utilizing a facile one-step hydrothermal technique, oxygen-deficient (o-BQ)-VO and (p-BQ)-VO nanosheets were synthesized, which were formulated as (o-BQ)0.25V2O5·0·5H2O and (p-BQ)0.25V2O5·0·5H2O (BQ = benzoquinone), respectively. Rietveld refinements and high-angle annular dark-field (HAADF)-scanning transmission election microscope (STEM) reveal the successful intercalation of o-BQ or p-BQ into the layered V2O5 with large interlayer spacings of ∼ 13.7 Å, in which all the V centers are coordinatively unsaturated due to the elongation of V-O bonds. (p-BQ)-VO shows an excellent rate performance of 487/446/405/371/333/280 mAh g−1 at 0.1 ∼ 5 A g−1 and an ultralong cycle life with a capacity retention of 96.0% after 4000 discharge/charge cycles at 5 A g−1, which is due to the dual redox-activity from BQ and vanadium oxide. The phenol-keto conversion of BQ can provide extra capacity. Furthermore, the sandwiched BQ in layered V2O5 can be prevented from leaching into the electrolyte. On the other hand, (p-BQ)-VO shows better electrochemical performance than (o-BQ)-VO, indicating that the redox property of quinone is associated with the para- or ortho-position of keto-group and their possible coordination modes with Zn2+. Density functional theory (DFT) calculations disclose that the deep intercalation of Zn2+ on certain site in (p-BQ)-VO can improve electron conductivity, giving rise to enhanced electrochemical behavior. And the Zn2+-migration along b axis of the (p-BQ)-VO cell shows a small energy barrier of 0.80 eV, thus leading to the outstanding rate and cycling performances. Redox-active benzoquinone (BQ)-intercalated layered vanadate (p-BQ)0.25V2O5·0·5H2O exhibits excellent rate performance and ultralong cycle life in zinc-ion battery, which is due to the dual redox-activity from BQ and vanadium oxide. Furthermore, the sandwiched BQ in layered V2O5 can be prevented from leaching into the electrolyte. DFT calculations disclose a small Zn2+-migration barrier of 0.80 eV. [Display omitted]
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2022.141447