Vanadium-based materials have been extensively studied as promising cathode materials for zinc-ion batteries because of their multiple valences and adjustable ion-diffusion channels. However, the sluggish kinetics of Zn-ion intercalation and less stable layered structure remain bottlenecks that limit their further development. The present work introduces potassium ions to partially substitute ammonium ions in ammonium vanadate, leading to a subtle shrinkage of lattice distance and the increased oxygen vacancies. The resulting potassium ammonium vanadate exhibits a high discharge capacity (464 mAh g at 0.1 A g) and excellent cycling stability (90% retention over 3000 cycles at 5 A g). The excellent electrochemical properties and battery performances are attributed to the rich oxygen vacancies. The introduction of K to partially replace NH appears to alleviate the irreversible deammoniation to prevent structural collapse during ion insertion/extraction. Density functional theory calculations show that potassium ammonium vanadate has a modulated electron structure and a better zinc-ion diffusion path with a lower migration barrier.
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http://dx.doi.org/10.1021/acsnano.1c11169 | DOI Listing |
Materials (Basel)
December 2024
School of Metallurgy, Northeastern University, Shenyang 110819, China.
Vanadium precipitation is the key step in producing vanadium products from vanadium solution. The sustainable development of the vanadium industry requires new environmentally friendly processes for vanadium precipitation. In this study, NaVO solution was pretreated with manganese salt to preliminarily separate the vanadium and sodium components.
View Article and Find Full Text PDFJ Hazard Mater
November 2024
Department of Chemical Engineering (Integrated Engineering Program), Kyung Hee University, Yongin 17104, South Korea; KHU-KIST Department of Converging Science and Technology, Kyung Hee University, Seoul 02447, South Korea. Electronic address:
PO guests anchored on metal vanadate hosts are as vital as SO/SO analogues in wide exploitation for expediting acidic/redox SCR cycles or ABS pyrolysis at low temperatures. This is due to their multiple roles as a provider of Brönsted acidic bonds (BA-H) and as a dictator of the traits for labile/mobile oxygens (O/O) and oxygen vacancies (O). However, the relationships of BA (P-O)/BA-H (P-O-H)/O/O/O feature for the host versus its mono-/bi-dentate PO binding mode ( [Formula: see text] / [Formula: see text] ) has never been examined to-date.
View Article and Find Full Text PDFMolecules
October 2024
Laboratory of Synthetic and Natural Medicinal Compounds Chemistry, A.B. Bekturov Institute of Chemical Sciences, 106 Sh. Ualikhanov St., Almaty 050010, Kazakhstan.
The synthesized compound, 1-(2-ethoxyethyl)-4-(pent-1-yn-1-yl)piperidin-4-yl propionate (), and its 1:1 complex with β-cyclodextrin () have been characterized for the first time through a comprehensive suite of analytical methods. This study explores the therapeutic potential of in modulating immune responses and accelerating the resolution of septic inflammation induced by chromium and vanadium ions in outbred male rats. The research highlights the significant impact of on the dynamics of regulatory T lymphocytes (Tregs), notably causing a reduction in the CD4CD25 fractions at the onset of inflammation.
View Article and Find Full Text PDFiScience
October 2024
Guangxi Key Laboratory of Information Materials, Guangxi Collaborative Innovation Center of Structure and Property for New Energy Materials, Guilin University of Electronic Technology, Guilin 541004, P.R. China.
In the past decade, vanadates have attracted one's attention as the electrode materials for aqueous zinc ion batteries (AZIBs). Nevertheless, their structural instability and sluggish ion/electron dynamics lead to an inevitable decline in the electrochemical performance. To address these issues, we introduce oxygen vacancies into NHVO nanosheets to improve the ion transport rate during the electrochemical reaction.
View Article and Find Full Text PDFAppl Spectrosc
September 2024
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
A combination of a highly efficient 213 nm Rayleigh rejection filter (RRF) and a miniaturized 213 nm neodymium-doped vanadate laser enables portable deep ultraviolet (UV) Raman spectrometers. We demonstrate the high efficiency of 213 nm RRF manufactured by Green Optics Co., Ltd by utilizing our compact 213 nm vanadate laser to measure high signal-to-noise ratio UV Raman spectra of Teflon and UV resonance Raman (UVRR) spectra of solid ammonium nitrate.
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