| Literature DB >> 28566497 |
Chongyin Yang1, Liumin Suo1, Oleg Borodin2, Fei Wang1, Wei Sun1, Tao Gao1, Xiulin Fan1, Singyuk Hou1, Zhaohui Ma1, Khalil Amine3, Kang Xu4, Chunsheng Wang5.
Abstract
Leveraging the most recent success in expanding the electrochemical stability window of aqueous electrolytes, in this work we create a unique Li-ion/sulfur chemistry of both high energy density and safety. We show that in the superconcentrated aqueous electrolyte, lithiation of sulfur experiences phase change from a high-order polysulfide to low-order polysulfides through solid-liquid two-phase reaction pathway, where the liquid polysulfide phase in the sulfide electrode is thermodynamically phase-separated from the superconcentrated aqueous electrolyte. The sulfur with solid-liquid two-phase exhibits a reversible capacity of 1,327 mAh/(g of S), along with fast reaction kinetics and negligible polysulfide dissolution. By coupling a sulfur anode with different Li-ion cathode materials, the aqueous Li-ion/sulfur full cell delivers record-high energy densities up to 200 Wh/(kg of total electrode mass) for >1,000 cycles at ∼100% coulombic efficiency. These performances already approach that of commercial lithium-ion batteries (LIBs) using a nonaqueous electrolyte, along with intrinsic safety not possessed by the latter. The excellent performance of this aqueous battery chemistry significantly promotes the practical possibility of aqueous LIBs in large-format applications.Entities:
Keywords: aqueous sulfur battery; gel polymer electrolyte; phase separation; rechargeable aqueous battery; water-in-salt
Year: 2017 PMID: 28566497 PMCID: PMC5474818 DOI: 10.1073/pnas.1703937114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205