Aqueous rechargeable zinc-sulfur (Zn-S) batteries are a promising, cost-effective, and high-capacity energy storage technology. Still, they are challenged by the poor reversibility of S cathodes, sluggish redox kinetics, low S utilization, and unsatisfactory areal capacity. This work develops a facile strategy to achieve an appealing high-areal-capacity (above 5 mAh cm) Zn-S battery by molecular-level regulation between S and high-electrical-conductivity tellurium (Te). The incorporation of Te as a dopant allows for manipulation of the Zn-S electrochemistry, resulting in accelerated redox conversion, and enhanced S utilization. Meanwhile, accompanied by the S-ZnS conversion, Te is converted to zinc telluride during the discharge process, as revealed by ex-situ characterizations. This additional redox reaction contributes to the S cathode's total excellent discharge capacity. With this unique cathode structure design, the carbon-confined TeS cathode (denoted as TeS/C) delivers a high reversible capacity of 1335.0 mAh g at 0.1 A g with a mass loading of 4.22 mg cm, corresponding to a remarkable areal capacity of 5.64 mAh cm. Notably, a hybrid electrolyte design uplifts discharge plateau, reduces overpotential, suppresses Zn dendrites growth, and extends the calendar life of Zn-TeS batteries. This study provides a rational S cathode structure to realize high-capacity Zn-S batteries for practical applications.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11187902 | PMC |
http://dx.doi.org/10.1002/advs.202308580 | DOI Listing |
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