A CaI<sub>2</sub>‐Based Electrolyte Enabled by Borate Ester Anion Receptors for Reversible Ca−Organic and Ca−Se Batteries
Abstract Passivating solid electrolyte interphases (SEIs) in Ca metal anodes constitute a long‐standing challenge, as they block Ca 2+ transport and inhibit reversible Ca deposition/stripping. Current solutions focus primarily on boron/aluminum‐based electrolytes to mitigate such interfacial issues by producing Ca 2+ ‐conductive species, yet the complex synthetic procedure of these salts restricts the widespread application. Moreover, whether any inorganic phases possess decent Ca 2+ conductivity within SEIs remains ambiguous. Herein, we report that a commercially available CaI 2 ‐dimethoxyethane electrolyte supports reversible Ca/Ca 2+ redox reactions via forming CaI 2 ‐involved SEI, inspired by our density functional theory calculations where CaI 2 species is predicted to possess the lowest Ca 2+ diffusion barrier among a range of inorganic phases. We further materialize this finding by introducing a serial of borate ester anion receptors, resulting in the formation of CaI 2 /borides hybrid SEIs with an enhanced Ca 2+ conductivity. Consequently, the resultant electrolytes realize a 7‐fold reduction in deposition/stripping overpotential compared to anion receptor‐free one, allowing for the construction of reversible Ca‐metal full cells with high‐capacity selenium and organic cathodes.
Authors
- Biao Zhang (ORCID: https://orcid.org/0000-0001-8687-8946)
- Zhen Hou (ORCID: https://orcid.org/0000-0002-0939-6115)
- Junwu Zhu (ORCID: https://orcid.org/0000-0002-7518-9683)
- Kai Liu (ORCID: https://orcid.org/0000-0001-8459-5184)
- Rui Zhou (ORCID: https://orcid.org/0000-0002-4297-8512)
Institutions
- Hong Kong Polytechnic University (HK)
- Nanjing University of Science and Technology (CN)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2024-09-20
- DOI
- https://doi.org/10.1002/ange.202413416
- Citations
- 1
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.21
Funders
- National Natural Science Foundation of China