Lithium-sulfur batteries (LSBs) are still limited by some issues such as polysulfides shuttle and lithium dendrites. Recently, the concept "high-entropy" has been considered as the research hotspot and international frontier. Herein, a high entropy MXene (TiVCrMoCT, HE-MXene) doped graphene is designed as the modified coating on commercial separators for LSBs. The HE-MXene affords multiple metal active sites, fast Li diffusion rate, and efficient adsorption toward polysulfide intermediates. Furthermore, strong lithophilic property is favorable for uniform Li deposition. The combination of in situ characterizations confirms TiVCrMoCT effectively promotes the LiS nucleation/dissolution kinetics, reduces the Li diffusion barrier, and exhibits favorable lithium uniform deposition behavior. This TiVCrMoCT/G@PP provides a high-capacity retention rate after 1000 cycles at 1 C and 2 C, with a capacity decay rate of merely 0.021% and 0.022% per cycle. Surprisingly, the cell operates at a low potential of 48 mV while maintaining at 5 mA cm/5 mAh cm for 4000 h. Furthermore, it still maintains a high-capacity retention rate under a high sulfur loading of 4.8/6.4 mg cm and a low E/S ratio of 8.6/7.5 µg mL. This work reveals a technical roadmap for simultaneously addressing the cathode and anode challenge, thus achieving potential commercially viable LSBs.
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http://dx.doi.org/10.1002/smll.202402344 | DOI Listing |
J Colloid Interface Sci
March 2023
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China. Electronic address:
Because of its high theoretical capacity and energy density, the lithium-sulfur (Li-S) battery is a desirable next-generation energy storage technology. However, the shuttle effect of lithium polysulfide and the slow sulfur reaction kinetics remain significant barriers to Li-S battery application. In this work, tantalum trisulfide (TaS) and selective manganese-doped tantalum trisulfide (Mn-TaS) nanocomposites on reduced graphene oxide surface were developed via a one-step hydrothermal method for the first time and introduced as a novel multifunctional mediator in the Li-S battery.
View Article and Find Full Text PDFSmall Methods
October 2021
State Key Laboratory of Chem/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.
The sulfur redox conversion with catalytically improved kinetics is promising to mitigate the polysulfides shuttling. While the size of electrocatalyst always brings different catalytic behaviors for various heterogeneous catalytic reactions, it is yet to be explored for Li-S batteries. Herein, a systematical study of size-dependent catalytic activity toward polysulfides conversion and the relevance to electrochemical performance are reported, by constructing Co catalysts with different atomic scales from single atoms, atomic clusters to nanoparticles.
View Article and Find Full Text PDFACS Appl Mater Interfaces
July 2021
State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.
Accelerating the redox reaction of polysulfides catalysis is an effective way to suppress the shuttling effect in lithium-sulfur (Li-S) cells. However, recent studies have mainly focused on the singular function of the catalyst, , either oxidation or reduction of polysulfides. As such, the goal of rapid cycling of sulfur species remains to be highly desired.
View Article and Find Full Text PDFSmall
October 2019
State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Science, Changchun, 130022, Jilin, China.
Lithium-sulfur (Li-S) batteries have been disclosed as one of the most promising energy storage systems. However, the low utilization of sulfur, the detrimental shuttling behavior of polysulfides, and the sluggish kinetics in electrochemical processes, severely impede their application. Herein, 3D hierarchical nitrogen-doped carbon nanosheets/molybdenum phosphide nanocrystal hollow nanospheres (MoP@C/N HCSs) are introduced to Li-S batteries via decorating commercial separators to inhibit polysulfides diffusion.
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