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The tremendous improvement in performance and cost of lithium-ion batteries (LIBs) have made them the technology of choice for electrical energy storage. While established battery chemistries and cell architectures for Li-ion batteries achieve good power and energy density, LIBs are unlikely to meet all the performance, cost, and scaling targets required for energy storage, in particular, in large-scale applications such as electrified transportation and grids. The demand to further reduce cost and/or increase energy density, as well as the growing concern related to natural resource needs for Li-ion have accelerated the investigation of so-called "beyond Li-ion" technologies. In this review, we will discuss the recent achievements, challenges, and opportunities of four important "beyond Li-ion" technologies: Na-ion batteries, K-ion batteries, all-solid-state batteries, and multivalent batteries. The fundamental science behind the challenges, and potential solutions toward the goals of a low-cost and/or high-energy-density future, are discussed in detail for each technology. While it is unlikely that any given new technology will fully replace Li-ion in the near future, "beyond Li-ion" technologies should be thought of as opportunities for energy storage to grow into mid/large-scale applications.
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http://dx.doi.org/10.1021/acs.chemrev.0c00767 | DOI Listing |
ACS Appl Energy Mater
August 2025
Centre for Cooperative Research on Alternative Energies (CIC energiGUNE), Basque Research and Technology Alliance (BRTA), Alava Technology Park, Albert Einstein 48, Vitoria-Gasteiz 01510 , Spain.
LiGaZrCl (LGZC) halides with high ionic conductivity (>0.4 mS/cm at 25 °C) are considered promising solid electrolytes for beyond Li-ion batteries. However, they suffer from low stability against the Li metal, forming a solid electrolyte interphase (SEI) that causes continuous degradation and limits their long-term cyclability.
View Article and Find Full Text PDFACS Appl Nano Mater
April 2025
Materials Electrochemistry Group, Department of Materials Science and Engineering, Drexel University, Philadelphia, Pennsylvania 19104, United States.
Bilayered vanadium oxides (BVOs) are promising cathode materials for beyond-Li-ion batteries due to their tunable chemistries and high theoretical capacities. However, the large size of beyond-Li ions limits electrochemical cycling and rate capability of BVO electrodes. Recent reports of MXene-derived BVOs with nanoscale flower-like morphology have shown improved electrochemical stability at high rates up to 5C in nonaqueous lithium-ion batteries.
View Article and Find Full Text PDFACS Appl Mater Interfaces
October 2024
Department of Chemical Sciences and Bernal Institute, University of Limerick, Limerick V94 T9PX, Ireland.
Magnesium-ion batteries (MIBs) are a "beyond Li-ion" technology that are hampered by Mg metal reactivity, which motivates the development of anode materials such as tin (Sn) with high theoretical capacity (903 mAh g). However, pure Sn is inactive for Mg storage. Herein, Mg alloying with Sn is enabled within dual-phase Bi-Sn anodes, where the optimal composition (BiSn) outperformed single-phase Bi and Sn electrodes to deliver high specific capacity (462 mAh g at 100 mA g), good cycle life (84% after 200 cycles), and significantly improved rate capability (403 mAh g at 1000 mA g).
View Article and Find Full Text PDFNanotechnology
September 2024
School of Mechanical and IT Engineering, Yeungnam University, Gyeongsan 38541, Republic of Korea.
Li-ion battery is currently considered to be the most proven technology for energy storage systems when it comes to the overall combination of energy, power, cyclability and cost. However, there are continuous expectations for cost reduction in large-scale applications, especially in electric vehicles and grids, alongside growing concerns over safety, availability of natural resources for lithium, and environmental remediation. Therefore, industry and academia have consequently shifted their focus towards 'beyond Li-ion technologies'.
View Article and Find Full Text PDFJ Am Chem Soc
June 2024
Department of Chemistry, Virginia Tech, Blacksburg, Virginia 24061, United States.
Traditional Li-ion intercalation chemistry into graphite anodes exclusively utilizes the cointercalation-free or cointercalation mechanism. The latter mechanism is based on ternary graphite intercalation compounds (t-GICs), where glyme solvents were explored and proved to deliver unsatisfactory cyclability in LIBs. Herein, we report a novel intercalation mechanism, that is, in situ synthesis of t-GIC in the tetrahydrofuran (THF) electrolyte via a spontaneous, controllable reaction between binary-GIC (b-GIC) and free THF molecules during initial graphite lithiation.
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