Mo-substitution in V<sub>2</sub>O<sub>5</sub> tunes the structure towards three-dimensional connectivity and improves Li-ion battery cycling

Abstract The development of alternative energy sources is crucial for reducing reliance on fossil fuels, particularly for mobile applications such as personal electronics and transportation. This necessitates the advancement of battery materials based on abundant and inexpensive constituent elements. To achieve this requires investigating materials in a broader compositional and structural design space. Early transition metal oxides, including the intercalation electrode <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi>α</mml:mi> <mml:mo>−</mml:mo> </mml:mrow> </mml:math> V 2 O 5 , however, the performance of V 2 O 5 is hindered by phase transformations during battery cycling that lead to capacity fade and short device lifetimes. This study investigates the modification of V 2 O 5 through Mo substitution in a series of the form V <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:msub> <mml:mrow/> <mml:mrow> <mml:mn>2</mml:mn> <mml:mo>−</mml:mo> <mml:mi>x</mml:mi> </mml:mrow> </mml:msub> </mml:mrow> </mml:math> Mo x O 5 for x = 0.05, 0.1, 0.2, 0.4, 0.6, and 0.8. X-ray diffraction data reveal progressive structural changes with increasing Mo content, which in turn change the progression of phase transformations during the first discharge. The different product also results in different cycling profile shapes that indicate differences in the charge storage mechanism as a function of Mo content. As a result, samples with higher Mo-substitution, especially V 1.2 Mo 0.8 O 5 , have narrower hysteresis, higher capacity, and improved capacity retention. While there is a limited solubility of Mo in the V 2 O 5 structure, with secondary phases and defects at many compositions, we show that Mo substitution alters the cycling behavior of V 2 O 5 to deep discharge, which can inform the design of intercalation materials for energy storage applications.

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Publication Details

Journal
Journal of Physics Materials
Published
2025-04-01
DOI
https://doi.org/10.1088/2515-7639/adc83e
Citations
3
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
2.19

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article

Mo-substitution in V2O5 tunes the structure towards three-dimensional connectivity and improves Li-ion battery cycling

B. Gardner, Shornam Gandhi, Kathryn A. Pitton, Beth S. Guiton et al.
3 citations
Journal of Physics Materials
Advancements in Battery Materials
2.19
article

Mo-substitution in V2O5 tunes the structure towards three-dimensional connectivity and improves Li-ion battery cycling

B. Gardner, Shornam Gandhi, Kathryn A. Pitton, Beth S. Guiton, Kausturi Parui, Juan C. Nino, Megan M. Butala, Noah G. Caracuel, Emily Vidal-Torres
article en
3 citations

Abstract

Abstract The development of alternative energy sources is crucial for reducing reliance on fossil fuels, particularly for mobile applications such as personal electronics and transportation. This necessitates the advancement of battery materials based on abundant and inexpensive constituent elements. To achieve this requires investigating materials in a broader compositional and structural design space. Early transition metal oxides, including the intercalation electrode <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:mi>α</mml:mi> <mml:mo>−</mml:mo> </mml:mrow> </mml:math> V 2 O 5 , however, the performance of V 2 O 5 is hindered by phase transformations during battery cycling that lead to capacity fade and short device lifetimes. This study investigates the modification of V 2 O 5 through Mo substitution in a series of the form V <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" overflow="scroll"> <mml:mrow> <mml:msub> <mml:mrow/> <mml:mrow> <mml:mn>2</mml:mn> <mml:mo>−</mml:mo> <mml:mi>x</mml:mi> </mml:mrow> </mml:msub> </mml:mrow> </mml:math> Mo x O 5 for x = 0.05, 0.1, 0.2, 0.4, 0.6, and 0.8. X-ray diffraction data reveal progressive structural changes with increasing Mo content, which in turn change the progression of phase transformations during the first discharge. The different product also results in different cycling profile shapes that indicate differences in the charge storage mechanism as a function of Mo content. As a result, samples with higher Mo-substitution, especially V 1.2 Mo 0.8 O 5 , have narrower hysteresis, higher capacity, and improved capacity retention. While there is a limited solubility of Mo in the V 2 O 5 structure, with secondary phases and defects at many compositions, we show that Mo substitution alters the cycling behavior of V 2 O 5 to deep discharge, which can inform the design of intercalation materials for energy storage applications.

Journal of Physics MaterialsVol. 8(2)
University of Kentucky (US), University of Florida (US), Michigan State University (US)
Division of Materials Research
Openalex Percentile: Top 13%
Advancements in Battery Materials
2.19
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