N, P Codoped Hollow Carbon Nanospheres Decorated with MoSe2 Ultrathin Nanosheets for Efficient Potassium-Ion Storage

材料科学 阳极 电化学 电解质 杂原子 化学工程 纳米结构 离子 纳米技术 退火(玻璃) 电极 碳纤维 复合材料 戒指(化学) 化学 有机化学 物理化学 复合数 工程类
作者
Lifeng Cui,Zhide Wang,Shifei Kang,Yanyan Fang,Ya Chen,Weikang Gao,Zhiyuan Zhang,Xin Gao,Chunyu Song,Xiaodong Chen,Yonggang Wang,Guoxiu Wang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (10): 12551-12561 被引量:26
标识
DOI:10.1021/acsami.1c24989
摘要

Potassium-ion batteries (KIBs) are gradually being considered as an alternative for lithium-ion batteries because of their non-negligible advantages such as abundance and low expenditure of K, as well as higher electrochemical potential than another alternative─sodium-ion batteries. Nevertheless, when the electrode materials are inserted and extracted with large-sized K+ ions, the tremendous volume change will cause the collapse of the microstructures of electrodes and make the charging/discharging process irreversible, thus disapproving their extended application. In response to this, we put forward a feasible strategy to realize the in situ assembly of layered MoSe2 nanosheets onto N, P codoped hollow carbon nanospheres (MoSe2/NP-HCNSs) through thermal annealing and heteroatom doping strategies, and the resulting nanoengineered material can function well as an anode for KIBs. This cleverly designed nanostructure of MoSe2/NP-HCNS can broaden the interlayer spacing of MoSe2 to boost the efficiency of the insertion/extraction of K ions and also can accommodate large volume change-caused mechanical strain, facilitate electrolyte penetration, and prevent the aggregation of MoSe2 nanosheets. This synthetic method generates abundant defects to increase the amounts of active sites, as well as conductivity. The hierarchical nanostructure can effectively increase the proportion of pseudo-capacitance and promote interfacial electronic transfer and K+ diffusion, thus imparting great electrochemical performance. The MoSe2/NP-HCNS anode exhibits a high reversible capacity of 239.9 mA h g-1 at 0.1 A g-1 after 200 cycles and an ultralong cycling life of 161.1 mA h g-1 at 1 A g-1 for a long period of 1000 cycles. This nanoengineering method opens up new insights into the development of promising anode materials for KIBs.
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