Resilient and Reversible Phosphotungstic Acid Passivated Zinc Anode

Aqueous zinc ion batteries (ZIBs) present a compelling solution for grid-scale energy storage, which is crucial for integrating renewable energy resources into the electric infrastructure. The cycling stability of ZIBs hinges on the electrochemical reversibility of the zinc anode, which is often compromised by corrosion and dendritic zinc deposition. Here, we present a straightforward surface passivation strategy that significantly enhances the cycling stability of zinc anodes. By immersing zinc in a solution of phosphotungstic acid, we promoted the dominance of the 002 plane of zinc's hexagonal structure. This process facilitates the creation of a uniform nucleation and protective layer on the native zinc surface, resulting in a more uniform plating-stripping process and increased corrosion resistance. In symmetric cells, the passivated zinc exhibits a capacity retention of 68.7% after 1000 cycles at a current density of 1.0 Ag<sup>1-</sup>, whereas untreated zinc anodes retain only 7.4% of capacity under identical conditions. In full cell zinc iodine batteries employing the passivated zinc anode, over 1000 stable charge-discharge cycles were achieved at a current density of 20 mA cm<sup>-2</sup>, with approximately 96% Coulombic efficiency (CE), 86% voltage efficiency (VE), and 82% energy efficiency (EE). This study demonstrates a promising pathway for the construction and upscaling of flow batteries with high capacity and low cost.

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Publication Details

Journal
Langmuir
Published
2024-08-05
DOI
https://doi.org/10.1021/acs.langmuir.4c01674
Citations
2
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
0.42

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article

Resilient and Reversible Phosphotungstic Acid Passivated Zinc Anode

Devendra Y. Nikumbe, Priyanka P. Bavdane, Rajaram Krishna Nagarale, Dimple K. Bora et al.
2 citations
Langmuir
Advanced battery technologies research
0.42
article

Resilient and Reversible Phosphotungstic Acid Passivated Zinc Anode

Devendra Y. Nikumbe, Priyanka P. Bavdane, Rajaram Krishna Nagarale, Dimple K. Bora, Pooja Madiyan
article en
2 citations

Abstract

Aqueous zinc ion batteries (ZIBs) present a compelling solution for grid-scale energy storage, which is crucial for integrating renewable energy resources into the electric infrastructure. The cycling stability of ZIBs hinges on the electrochemical reversibility of the zinc anode, which is often compromised by corrosion and dendritic zinc deposition. Here, we present a straightforward surface passivation strategy that significantly enhances the cycling stability of zinc anodes. By immersing zinc in a solution of phosphotungstic acid, we promoted the dominance of the 002 plane of zinc's hexagonal structure. This process facilitates the creation of a uniform nucleation and protective layer on the native zinc surface, resulting in a more uniform plating-stripping process and increased corrosion resistance. In symmetric cells, the passivated zinc exhibits a capacity retention of 68.7% after 1000 cycles at a current density of 1.0 Ag<sup>1-</sup>, whereas untreated zinc anodes retain only 7.4% of capacity under identical conditions. In full cell zinc iodine batteries employing the passivated zinc anode, over 1000 stable charge-discharge cycles were achieved at a current density of 20 mA cm<sup>-2</sup>, with approximately 96% Coulombic efficiency (CE), 86% voltage efficiency (VE), and 82% energy efficiency (EE). This study demonstrates a promising pathway for the construction and upscaling of flow batteries with high capacity and low cost.

LangmuirVol. 40(33)
Central Salt and Marine Chemicals Research Institute (IN), Academy of Scientific and Innovative Research (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Council of Scientific and Industrial Research, India
Openalex Percentile: Top 39%
Advanced battery technologies research
0.42
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Resilient and Reversible Phosphotungstic Acid Passivated Zinc Anode — Devendra Y. Nikumbe, Priyanka P. Bavdane, et al. · Langmuir (2024) | TGRS Research Map | TGRS