Carbon-encapsulated ultrathin MoS2 nanosheets epitaxially grown on porous metallic TiNb2O6 microspheres with unsaturated oxygen atoms for superior potassium storage

Rechargeable potassium-ion batteries (KIBs) have emerged as promising alternatives to lithium-ion batteries (LIBs) in large-scale applications due to the abundant and low-cost potassium resources. To date, only a few suitable potassium storage materials have been reported due to the large-sized pota...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (10), p.5760-5768
Hauptverfasser: Xing, Lidong, Yu, Qiyao, Jiang, Bo, Chu, Jianhua, Cheng-Yen Lao, Wang, Min, Han, Kun, Liu, Zhiwei, Bao, Yanping, Wei (Alex) Wang
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Sprache:eng
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Zusammenfassung:Rechargeable potassium-ion batteries (KIBs) have emerged as promising alternatives to lithium-ion batteries (LIBs) in large-scale applications due to the abundant and low-cost potassium resources. To date, only a few suitable potassium storage materials have been reported due to the large-sized potassium ions and sluggish kinetics. Herein, we design a three-layered heterostructure with porous metallic TiNb2O6 as the core and carbon-encapsulated MoS2 nanosheets as the shell (denoted as TiNb2O6@MoS2/C) as an advanced anode for KIBs. This hybrid configuration can significantly enhance the electronic conductivity from the interior to the exterior by virtue of the oxygen-atom-unsaturated metallic TiNb2O6 core. Furthermore, the amorphous carbon shell plays a crucial role to inhibit the particle agglomeration, accommodate the volume expansion and protect the active material from pulverization because of the three-layered heterostructure. As a result, impressive electrochemical behavior with high capacity (424 mA h g−1 at 0.1 A g−1 after 50 cycles) and high cycling stability (175 mA h g−1 at 1.0 A g−1 after 300 cycles) is achieved. This work opens the door for designing highly conductive heterostructures for energy storage devices.
ISSN:2050-7488
2050-7496
DOI:10.1039/c8ta12497c