Interface-engineered metallic 1T-MoS2 nanosheet array induced via palladium doping enabling catalysis enhancement for lithium–oxygen battery
The phase structure conversion of 2H- to 1T- MoS2 was achieved by Pd interfacial engineering and the Pd-TMS/CT electrode was investigated in Li–O2 system for the first time. [Display omitted] •Phase transforming of MoS2 is induced by a spontaneous interfacial redox strategy.•Pd-doping induced metall...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-02, Vol.382, p.122854, Article 122854 |
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Sprache: | eng |
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Zusammenfassung: | The phase structure conversion of 2H- to 1T- MoS2 was achieved by Pd interfacial engineering and the Pd-TMS/CT electrode was investigated in Li–O2 system for the first time.
[Display omitted]
•Phase transforming of MoS2 is induced by a spontaneous interfacial redox strategy.•Pd-doping induced metallic 1T-MoS2 nanosheet array is investigated in Li–O2 battery.•Assembled 1T-MoS2-based battery leads to a striking improvement of Li–O2 batteries.•Fabricated flexible pouch-type battery can stably operate under vary conditions.
Lacking strategy to enhance the intrinsic catalytic activity and site density of hexagonal molybdenum disulfide (2H-MoS2) is restricting their further development as viable electrocatalysts for lithium–oxygen (Li–O2) battery. Here, palladium (Pd) induced metallic (1T) MoS2 nanosheet array supported on carbon textiles (Pd-TMS/CT) was deliberately fabricated as a high-efficient freestanding cathode of Li–O2 battery. Transforming semiconducting 2H phase to the stabilized metallic 1T phase of MoS2 was induced by doping Pd using a spontaneous interfacial redox strategy. This novel class of 1T-MoS2 nanosheet array with unique electronic structures enables the electrode with fast reaction kinetics, high electrical transport rate, and proliferated catalytic active sites, which lead to a striking improvement of their intrinsic catalytic behavior in Li–O2 battery. In addition, the synergistic effect with well-designed surface chemistry of MoS2 is favorable for the reversible formation and decomposition of products and the inhibition of side reactions on Pd-TMS/CT cathode. As a result, the battery with Pd-TMS/CT exhibits outstanding electrochemical behavior in terms of high discharge capacity of 7441 mA h g−1, low overpotential, and especially the excellent electrochemical stability for over 2488 h (622 cycles). Moreover, due to its flexibility superiority, the assembled pouch-type battery based on Pd-TMS/CT cathode can stably operate in real air atmosphere under different bending and twisting conditions, which opens up a variety of potential applications of flexible devices with high energy density. |
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ISSN: | 1385-8947 1873-3212 |
DOI: | 10.1016/j.cej.2019.122854 |