A layered Prussian blue analogue as fast-charging negative electrode material for lithium-ion batteries
Chongwei Gao,
Ming Chen,
Jiantao Li,
Sungsik Lee,
Tian Sun,
Xunan Wang,
Shuhua Zhang,
Guang Feng (),
Dengyun Zhai () and
Feiyu Kang ()
Additional contact information
Chongwei Gao: Tsinghua University, Shenzhen Geim Graphene Center, Institute of Materials Research, Tsinghua Shenzhen International Graduate School
Ming Chen: Huazhong University of Science and Technology, State Key Laboratory of Coal Combustion and School of Energy and Power Engineering
Jiantao Li: Argonne National Laboratory, Chemical Sciences and Engineering Division
Sungsik Lee: Argonne National Laboratory, X-ray Science Division, Advanced Photon Source
Tian Sun: Huazhong University of Science and Technology, State Key Laboratory of Coal Combustion and School of Energy and Power Engineering
Xunan Wang: Tsinghua University, Shenzhen Geim Graphene Center, Institute of Materials Research, Tsinghua Shenzhen International Graduate School
Shuhua Zhang: Tsinghua University, Shenzhen Geim Graphene Center, Institute of Materials Research, Tsinghua Shenzhen International Graduate School
Guang Feng: Huazhong University of Science and Technology, State Key Laboratory of Coal Combustion and School of Energy and Power Engineering
Dengyun Zhai: Tsinghua University, Shenzhen Geim Graphene Center, Institute of Materials Research, Tsinghua Shenzhen International Graduate School
Feiyu Kang: Tsinghua University, Shenzhen Geim Graphene Center, Institute of Materials Research, Tsinghua Shenzhen International Graduate School
Nature Communications, 2025, vol. 16, issue 1, 1-13
Abstract:
Abstract The simultaneous achievement of fast-charging and high specific capacity remains a critical challenge for lithium-ion battery negative electrodes. Here we report a layered manganese-based Prussian blue analogue, synthesized through vacancy control and subsequent thermal transformation. As a conversion-type negative electrode, this material exhibits high-rate performance, delivering a specific capacity of 510 mAh g−1 at a specific current of 8 A g−1, and operates at a moderate average voltage of approximately 1.2 V vs. Li/Li+, which mitigates lithium plating risks. This high-rate capability stems from the analogue’s specific linkage configurations, which facilitate a high content of active transition metal and strong Li+ adsorption at nitrogen sites. The high transition metal content enables a high reversible capacity, while strong Li+ adsorption promotes an efficient initial crystalline-to-amorphous transformation. This process induces dynamically reversible component migration during subsequent cycling, thereby enhancing conversion reaction kinetics. Our findings provide insights into the application of Prussian blue analogues as fast-charging negative electrode materials.
Date: 2025
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DOI: 10.1038/s41467-025-65250-9
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