Abstract

The notorious shuttling behaviors and sluggish conversion kinetics of the intermediate lithium polysulfides (LPS) are hindering the practical application of lithium sulfur (Li-S) batteries. Herein, an ultrafine, amorphous and oxygen-deficient niobium pentoxide nanocluster embedded in microporous carbon nanospheres (A-Nb2O5-x@MCS) was developed as multifunctional sulfur immobilizer and promoter toward superior shuttle inhibition and conversion catalyzation of LPS. The A-Nb2O5-x nanocluster implanted framework uniformizes sulfur distribution, exposes vast active interfaces and offers reduced ion/electron transportation pathway for expedited redox reaction. Moreover, the low crystallinity feature of A-Nb2O5-x manipulates the LPS chemical affinity while the defect chemistry enhances the intrinsic conductivity and catalytic activity for rapid electrochemical conversions. Attributed to these unique superiorities, A-Nb2O5-x@MCS enables remarkable Li-S battery performances, i.e., high areal capacity of 6.62 mAh cm-2 under high sulfur loading and low electrolyte/sulfur ratio, superb rate capability and outstanding cyclability over 1200 cycles with ultra-low capacity fading rate of 0.024 % per cycle. This work provides a synergistic regulation on crystallinity and oxygen-deficiency towards rapid and durable sulfur electrochemistry, holding a great promise in developing practically viable Li-S batteries and enlightening material engineering in related energy storage and conversion areas.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.