Preparation and Electrochemical Characteristics of the Co-Doped Li7La3Zr2O12 Solid Electrolyte with Fe3+ and Bi3+

Solid-state electrolytes (SSEs) have emerged as the most promising alternative to liquid electrolytes in batteries due to their enhanced stability and safety. Among these, the garnet-type Li<sub>7</sub>La<sub>3</sub>Zr<sub>2</sub>O<sub>12</sub> (LLZO) solid electrolyte has attracted significant research interest due to its wide electrochemical stability window and good air stability. However, the ionic conductivity of LLZO is lower due to its high sintering temperature and unstable phase structure. In this study, Li<sub>6.4+x</sub>Fe<sub>0.2</sub>La<sub>3</sub>Zr<sub>2-x</sub>Bi<sub>x</sub>O<sub>12</sub> (x = 0, 0.05, 0.1, 0.15) solid electrolytes were synthesized using a conventional solid-state reaction method by co-doping LLZO with Fe<sup>3+</sup> and Bi<sup>3+</sup> ions. Compared with pure LLZO, doping with Fe<sup>3+</sup> effectively stabilizes the cubic phase, thereby enhancing the ionic conductivity. Moreover, Bi<sup>3+</sup> doping significantly lowers the sintering temperature of the electrolyte, which in turn reduces energy consumption during the processing. The co-doping of Fe<sup>3+</sup> and Bi<sup>3+</sup> not only improves the density of the LLZO electrolyte, achieving a relative density of up to 95%, but also increases the ionic conductivity, with a maximum value of 7.57 × 10<sup>-4</sup> S·cm<sup>-1</sup> observed at the optimal composition (Li<sub>6.4+x</sub>Fe<sub>0.2</sub>La<sub>3</sub>Zr<sub>2-x</sub>Bi<sub>x</sub>O<sub>12</sub>, x = 0.1).

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Publication Details

Journal
Molecules
Published
2025-05-02
DOI
https://doi.org/10.3390/molecules30092028
Citations
2
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
1.46
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article

Preparation and Electrochemical Characteristics of the Co-Doped Li7La3Zr2O12 Solid Electrolyte with Fe3+ and Bi3+

Ke Xue, Xingyu Duan, Jiuhui Qu, Shengli An
2 citations
Molecules
Advanced Battery Materials and Technologies
1.46
article

Preparation and Electrochemical Characteristics of the Co-Doped Li7La3Zr2O12 Solid Electrolyte with Fe3+ and Bi3+

Ke Xue, Xingyu Duan, Jiuhui Qu, Shengli An
article en
2 citations

Abstract

Solid-state electrolytes (SSEs) have emerged as the most promising alternative to liquid electrolytes in batteries due to their enhanced stability and safety. Among these, the garnet-type Li<sub>7</sub>La<sub>3</sub>Zr<sub>2</sub>O<sub>12</sub> (LLZO) solid electrolyte has attracted significant research interest due to its wide electrochemical stability window and good air stability. However, the ionic conductivity of LLZO is lower due to its high sintering temperature and unstable phase structure. In this study, Li<sub>6.4+x</sub>Fe<sub>0.2</sub>La<sub>3</sub>Zr<sub>2-x</sub>Bi<sub>x</sub>O<sub>12</sub> (x = 0, 0.05, 0.1, 0.15) solid electrolytes were synthesized using a conventional solid-state reaction method by co-doping LLZO with Fe<sup>3+</sup> and Bi<sup>3+</sup> ions. Compared with pure LLZO, doping with Fe<sup>3+</sup> effectively stabilizes the cubic phase, thereby enhancing the ionic conductivity. Moreover, Bi<sup>3+</sup> doping significantly lowers the sintering temperature of the electrolyte, which in turn reduces energy consumption during the processing. The co-doping of Fe<sup>3+</sup> and Bi<sup>3+</sup> not only improves the density of the LLZO electrolyte, achieving a relative density of up to 95%, but also increases the ionic conductivity, with a maximum value of 7.57 × 10<sup>-4</sup> S·cm<sup>-1</sup> observed at the optimal composition (Li<sub>6.4+x</sub>Fe<sub>0.2</sub>La<sub>3</sub>Zr<sub>2-x</sub>Bi<sub>x</sub>O<sub>12</sub>, x = 0.1).

MoleculesVol. 30(9)
Guizhou University (CN), Inner Mongolia University of Science and Technology (CN)
Affordable and clean energy
Openalex Percentile: Top 18%
Advanced Battery Materials and Technologies
1.46
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Preparation and Electrochemical Characteristics of the Co-Doped Li7La3Zr2O12 Solid Electrolyte with Fe3+ and Bi3+ — Ke Xue, Xingyu Duan, et al. · Molecules (2025) | TGRS Research Map | TGRS