Developing high-power Li||S batteries via transition metal/carbon nanocomposite electrocatalyst engineering.
Huan LiRongwei MengChao YeAnton TadichWuxing HuaQin-Fen GuBernt JohannessenXiao ChenKenneth DaveyShi-Zhang QiaoPublished in: Nature nanotechnology (2024)
The activity of electrocatalysts for the sulfur reduction reaction (SRR) can be represented using volcano plots, which describe specific thermodynamic trends. However, a kinetic trend that describes the SRR at high current rates is not yet available, limiting our understanding of kinetics variations and hindering the development of high-power Li||S batteries. Here, using Le Chatelier's principle as a guideline, we establish an SRR kinetic trend that correlates polysulfide concentrations with kinetic currents. Synchrotron X-ray adsorption spectroscopy measurements and molecular orbital computations reveal the role of orbital occupancy in transition metal-based catalysts in determining polysulfide concentrations and thus SRR kinetic predictions. Using the kinetic trend, we design a nanocomposite electrocatalyst that comprises a carbon material and CoZn clusters. When the electrocatalyst is used in a sulfur-based positive electrode (5 mg cm -2 of S loading), the corresponding Li||S coin cell (with an electrolyte:S mass ratio of 4.8) can be cycled for 1,000 cycles at 8 C (that is, 13.4 A g S -1 , based on the mass of sulfur) and 25 °C. This cell demonstrates a discharge capacity retention of about 75% (final discharge capacity of 500 mAh g S -1 ) corresponding to an initial specific power of 26,120 W kg S -1 and specific energy of 1,306 Wh kg S -1 .
Keyphrases
- transition metal
- solid state
- ion batteries
- single cell
- aqueous solution
- high resolution
- cell therapy
- carbon nanotubes
- metal organic framework
- magnetic resonance imaging
- reduced graphene oxide
- genome wide
- single molecule
- highly efficient
- gene expression
- magnetic resonance
- computed tomography
- bone marrow
- mass spectrometry
- dna methylation
- solid phase extraction