Synthetic heterostructure enhances specific capacity in lithium-ion and sodium-ion batteries, indicating promising performance.
Transition metal selenides have emerged as attractive negative electrode candidates for rechargeable lithium‐/sodium‐ion batteries (LIBs/SIBs) thanks to their superior theoretical energy storage capability. Unfortunately, their practical application faces significant challenges due to low conductivity, structural degradation from volume changes, and sluggish ion diffusion kinetics. Herein, a nitrogen‐doped carbon (NC) coated Cu 2 Se‐CoSe 2 heterostructure, which is embedded in reduced graphene oxide (rGO) sheets (Cu 2 Se‐CoSe 2 @NC@rGO), is synthesized. Cu 2 Se‐CoSe 2 @NC@rGO nanospheres possess a high specific surface area of 207.02 m 2 g −1 , which provides ample active sites for ion reactions. The heterojunction between Cu 2 Se and CoSe 2 creates a built‐in electric field, which is conducive to ion and electron transport. Additionally, NC shell and rGO matrix work synergistically to suppress volume expansion and enhance structural stability. In LIBs, it has a considerable specific capacity (1161.6 mA h g −1 after 200 cycles at 0.2 A g −1 ) and good cycling stability (1261.1 mA h g −1 after 500 cycles at 1 A g −1 ). In SIBs, it maintains 422.4 mA h g −1 under 0.1 A g −1 after 200 cycles. These advancements demonstrate the promise of Cu 2 Se‐CoSe 2 @NC@rGO as a promising anode in LIBs and SIBs.
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Zhang et al. (2025) studied this question.
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