Abstract
Lithium-sulfur (Li-S) batteries are promising next-generation energy storage devices because of their high energy density of 2600 Wh kg-1. Efficient immobilization and fast conversion of soluble lithium polysulfide intermediates (LiPSs) are crucial to the electrochemical performance of Li-S batteries. Herein, we report a novel strategy to simultaneously achieve large capacity, high rate capability, and long cycle life by utilizing mesoporous niobium nitride microspheres/N-doped graphene nanosheets (NbN@NG) hybrids as multifunctional host materials for sulfur cathodes. The mesoporous NbN microspheres chemically immobilize LiPSs via Nb-S chemical bonding and catalytically promote conversion of LiPSs into insoluble Li2S resulting in enhanced redox reaction kinetics. Moreover, the highly conductive NbN and N-doped graphene nanosheets provide rapid electron transport and consequently, the S/NbN@NG cathode demonstrates a large capacity of 948 mAh g-1 at 1C (1C = 1650 mA g-1), high rate capability of 739 mAh g-1 at 5C, and excellent cycle stability with a capacity decay of 0.09% per cycle for over 400 cycles. The results described here provide insights into the design of multifunctional host materials for high-performance Li-S batteries.
| Original language | English |
|---|---|
| Journal | ACS Applied Materials and Interfaces |
| Volume | 11 |
| Issue number | 3 |
| Online published | 2 Jan 2019 |
| DOIs | |
| Publication status | Published - 23 Jan 2019 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 7 Affordable and Clean Energy
Research Keywords
- chemical absorption
- electrocatalytic conversion
- lithium-sulfur batteries
- niobium nitride
- polysulfide trapping
Fingerprint
Dive into the research topics of 'Conductive Mesoporous Niobium Nitride Microspheres/Nitrogen-Doped Graphene Hybrid with Efficient Polysulfide Anchoring and Catalytic Conversion for High-Performance Lithium-Sulfur Batteries'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver