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High-Mass-Loading Anode-Free Lithium–Sulfur Batteries Enabled by a Binary Binder with Fast Lithium-Ion Transport AITranslate

The University of Texas at Austin; The University of Texas at Austin; The University of Texas at Austin
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Publisher: ACS
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Abstract AITranslate

To realize the practical viability of lithium–sulfur batteries (LSBs), it is crucial to develop advanced electrode materials that enable high-mass-loading cells with limited lithium and a lean electrolyte. We present here the design of a binary binder by combining poly(ethylene oxide) (PEO) with a cross-linked quadripolymer, which exhibits high mechanical strength and electrochemical stability. The tightly interwoven binder network enhances the structural reliability of PEO in ether-based electrolytes and the resilience of the electrode to accommodate volume changes during cycling. Moreover, the anode–electrolyte interfacial chemistry and the sulfur redox kinetics are ameliorated by this binder due to its strong polysulfide adsorbability and the multiple lithium-ion transport channels in the PEO matrix and quadripolymer skeleton. With this binder, anode-free full cells with a Li2S loading of 5.4 mg cm–2 and a low electrolyte/sulfur ratio of 7 μL mg–1 display a significantly improved capacity retention of 79% after 100 cycles.

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DOI:https://doi.org/10.1021/acsenergylett.3c01395

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Citation Information:

To realize the practical viability of lithium–sulfur batteries (LSBs), it is crucial to develop advanced electrode materials that enable high-mass-loading cells with limited lithium and a lean electrolyte. We present here the design of a binary binder by combining poly(ethylene oxide) (PEO) with a cross-linked quadripolymer, which exhibits high mechanical strength and electrochemical stability. The tightly interwoven binder network enhances the structural reliability of PEO in ether-based electrolytes and the resilience of the electrode to accommodate volume changes during cycling. Moreover, the anode–electrolyte interfacial chemistry and the sulfur redox kinetics are ameliorated by this binder due to its strong polysulfide adsorbability and the multiple lithium-ion transport channels in the PEO matrix and quadripolymer skeleton. With this binder, anode-free full cells with a Li2S loading of 5.4 mg cm–2 and a low electrolyte/sulfur ratio of 7 μL mg–1 display a significantly improved capacity retention of 79% after 100 cycles.

quote

GB/T 7714-2015 [1] Biyu Jin, Tianxing Lai, Arumugam Manthiram. ACS Energy Letters, 2023(8). DOI:10.1021/acsenergylett.3c01395.
MLA [1] Biyu Jin, et al., ACS Energy Letters, no. 8, 2023, https://doi.org/10.1021/acsenergylett.3c01395.
APA [1] Biyu Jin, Tianxing Lai, & Arumugam Manthiram. (2023). ACS Energy Letters(8). https://doi.org/10.1021/acsenergylett.3c01395
IEEE [1] Biyu Jin, Tianxing Lai, and Arumugam Manthiram, ACS Energy Letters, no. 8, 2023, doi: 10.1021/acsenergylett.3c01395.