Abundant Cu<sub>3</sub>P/Co<sub>2</sub>P/CoP@NC Heterostructures Boost Charge Transfer Toward Fast and Durable Sodium Storage

ABSTRACT Heterogeneous structure and carbon coating are important ways to enhance the reaction kinetics and cycling stability of metal phosphides as anode materials for sodium‐ion batteries. Therefore, nitrogen‐doped carbon‐capped triphasic heterostructure Cu 3 P/Co 2 P/CoP@NC stands for nitrogen doped carbon nanorods were designed and synthesized through a combination of phosphide and carbonization. Kinetic analyses (cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic intermittent titration technique) and density functional theory calculations show that the three‐phase heterostructure and carbon layer effectively improve Na adsorption and migration as well as the electrochemical reactivity of the electrode. Based on this, Cu 3 P/Co 2 P/CoP@NC demonstrated excellent rate performance (305.9 mAh g −1 at 0.3 A g −1 and 202.8 mAh g −1 even at 10 A g −1 ) and cycling stability (the capacity decay rate is only 0.12% from the 5th to 300th cycle) when it is used for sodium‐ion battery anodes. The in situ X‐ray diffraction, ex situ X‐ray photoelectron spectroscopy, and high‐resolution transmission electron microscopy tests showed that Cu 3 P/Co 2 P/CoP@NC is based on a conversion reaction mechanism for sodium‐ion storage. In addition, the NVP@reduced graphene oxide (rGO)//Cu 3 P/Co 2 P/CoP@NC full‐cell delivers a high capacity of 210.2 mAh g −1 after 50 cycles at 0.3 A g −1 . This work can provide a reference for the design of high‐performance sodium electrode anode materials.

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Publication Details

Journal
Carbon Energy
Published
2025-03-26
DOI
https://doi.org/10.1002/cey2.721
Citations
25
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
18.26
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Abundant Cu3P/Co2P/CoP@NC Heterostructures Boost Charge Transfer Toward Fast and Durable Sodium Storage

Zhongchao Bai, Yanjun Zhai, Yunxiu Wang, Shi Xue Dou et al.
25 citations
Carbon Energy
Advancements in Battery Materials
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article

Abundant Cu3P/Co2P/CoP@NC Heterostructures Boost Charge Transfer Toward Fast and Durable Sodium Storage

Zhongchao Bai, Yanjun Zhai, Yunxiu Wang, Shi Xue Dou, Zhenhua Yan, Ming Yue Wang, Fuyi Jiang, Wei Du, Nana Wang, Yifan Zhang, Yuzhang Zhou, Caifu Dong
article en
25 citations

Abstract

ABSTRACT Heterogeneous structure and carbon coating are important ways to enhance the reaction kinetics and cycling stability of metal phosphides as anode materials for sodium‐ion batteries. Therefore, nitrogen‐doped carbon‐capped triphasic heterostructure Cu 3 P/Co 2 P/CoP@NC stands for nitrogen doped carbon nanorods were designed and synthesized through a combination of phosphide and carbonization. Kinetic analyses (cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic intermittent titration technique) and density functional theory calculations show that the three‐phase heterostructure and carbon layer effectively improve Na adsorption and migration as well as the electrochemical reactivity of the electrode. Based on this, Cu 3 P/Co 2 P/CoP@NC demonstrated excellent rate performance (305.9 mAh g −1 at 0.3 A g −1 and 202.8 mAh g −1 even at 10 A g −1 ) and cycling stability (the capacity decay rate is only 0.12% from the 5th to 300th cycle) when it is used for sodium‐ion battery anodes. The in situ X‐ray diffraction, ex situ X‐ray photoelectron spectroscopy, and high‐resolution transmission electron microscopy tests showed that Cu 3 P/Co 2 P/CoP@NC is based on a conversion reaction mechanism for sodium‐ion storage. In addition, the NVP@reduced graphene oxide (rGO)//Cu 3 P/Co 2 P/CoP@NC full‐cell delivers a high capacity of 210.2 mAh g −1 after 50 cycles at 0.3 A g −1 . This work can provide a reference for the design of high‐performance sodium electrode anode materials.

Carbon EnergyVol. 7(6)
University of Shanghai for Science and Technology (CN), Yantai University (CN), Liaocheng University (CN), University of Wollongong (AU), Nankai University (CN)
Openalex Percentile: Top 1%
Advancements in Battery Materials
18.26
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