The formation of crystalline lithium sulfide on electrocatalytic surfaces in lithium–sulfur batteries
| Autor: | Meng Zhao, Li-Peng Hou, Hong-Jie Peng, Chang-Xin Zhao, Yun-Wei Song, Bo-Quan Li, Yan-Qi Peng, Jin-Lei Qin |
|---|---|
| Rok vydání: | 2022 |
| Předmět: |
Battery (electricity)
Materials science Energy Engineering and Power Technology chemistry.chemical_element 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology Electrocatalyst 01 natural sciences Sulfur Redox 0104 chemical sciences Amorphous solid chemistry.chemical_compound Fuel Technology Lithium sulfide chemistry Chemical engineering Electrochemistry 0210 nano-technology Polysulfide Energy (miscellaneous) Sulfur utilization |
| Zdroj: | Journal of Energy Chemistry. 64:568-573 |
| ISSN: | 2095-4956 |
| DOI: | 10.1016/j.jechem.2021.05.023 |
| Popis: | Lithium–sulfur (Li–S) battery is highly regarded as a promising next-generation energy storage device but suffers from sluggish sulfur redox kinetics. Probing the behavior and mechanism of the sulfur species on electrocatalytic surface is the first step to rationally introduce polysulfide electrocatalysts for kinetic promotion in a working battery. Herein, crystalline lithium sulfide (Li2S) is exclusively observed on electrocatalytic surface with uniform spherical morphology while Li2S on non-electrocatalytic surface is amorphous and irregular. Further characterization indicates the crystalline Li2S preferentially participates in the discharge/charge process to render reduced interfacial resistance, high sulfur utilization, and activated sulfur redox reactions. Consequently, crystalline Li2S is proposed with thermodynamic and kinetic advantages to rationalize the superior performances of Li–S batteries. The evolution of solid Li2S on electrocatalytic surface not only addresses the polysulfide electrocatalysis strategy, but also inspires further investigation into the chemistry of energy-related processes. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect