Enhanced alkali-metal ion storage performance of bimetallic selenide/ N-doped carbon core-shell anodes

被引:1
作者
Kim, Hongjung [1 ,2 ]
Song, Yuna [1 ]
Kim, Minkyu [1 ]
Jeong, Yunji [1 ]
Kim, Moonsu [1 ]
Lee, Gibaek [1 ]
机构
[1] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
[2] Pohang Univ Sci & Technol POSTECH, Chem Engn, Pohang 37673, Gyeongbuk, South Korea
基金
新加坡国家研究基金会;
关键词
Transition metal selenide; N -doped carbon; Heterojunction; Lithium-ion battery; Potassium-ion battery; SOLID-ELECTROLYTE INTERPHASE; REDUCED GRAPHENE OXIDE; HIGH-CAPACITY; ORGANIC FRAMEWORK; FLUOROETHYLENE CARBONATE; ENERGY-STORAGE; LITHIUM; BATTERY; NANOPARTICLES; COMPOSITES;
D O I
10.1016/j.cej.2024.158750
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this research, we developed a ZnSe@Co0.85Se heterojunction embedded in N-doped carbon (NC), derived from a zeolitic imidazolate framework (ZIF), for use in lithium-ion batteries (LIBs). The material, ZnSeNC@Co0.85SeNC, exhibited excellent cycling and rate performance, achieving capacities of 944.1 mAh g-1 at 1.0 A g-1 and 277.6 mAh g-1 at 10 A g-1. Full-cell tests demonstrated its effectiveness, with a specific capacity of approximately 80 mAh/g, coulombic efficiency near 99 %, and capacity retention of 64 %, corresponding to power and energy densities of 97.2 W kg- 1 and 224 Wh kg- 1, respectively. We explored the capacity enhancement mechanisms, identifying factors such as activation of crystalline Se, formation of a Se-rich solid-electrolyte interface, and capacitive contributions from reduced metal particles. Computational studies indicated that these improvements were linked to the heterojunction interface of ZnSe, Co0.85Se, and NC. Additionally, the material's potential for potassium-ion battery (PIB) applications was assessed, delivering 274.8 mAh g-1 at 1.0 A g-1. This work not only advances our understanding of transition-metal selenides (TMSe) in battery applications but also proposes design strategies for TMSe-based materials for both LIB and PIB anodes.
引用
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页数:16
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