2019
DOI: 10.1039/c9ta01500k
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Perovskite-type La0.56Li0.33TiO3as an effective polysulfide promoter for stable lithium–sulfur batteries in lean electrolyte conditions

Abstract: Lithium–sulfur batteries (LSBs) are promising candidates for next-generation energy storage equipment due to their high theoretical energy density.

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Cited by 53 publications
(39 citation statements)
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“…Quick ion conductor La 0.56 Li 0.33 TiO 3 with perovskite structure reciprocates the excellent electrochemical performances of LSBs due to the favorable interfacial affinity of lithiophilic (O) and sulfiphilic (Ti) sites toward LiPSs as shown in Fig. 13(a) [124]. Besides, the excellent ionic conductivity of 2.94 Â 10 -4 S cm À1 and the outstanding electrocatalytic role for the redox conversion of polysulfides significantly suppress the shuttle effect, accelerate reaction kinetics, and reduce overpotential during charge/discharge process.…”
Section: Othersmentioning
confidence: 95%
See 1 more Smart Citation
“…Quick ion conductor La 0.56 Li 0.33 TiO 3 with perovskite structure reciprocates the excellent electrochemical performances of LSBs due to the favorable interfacial affinity of lithiophilic (O) and sulfiphilic (Ti) sites toward LiPSs as shown in Fig. 13(a) [124]. Besides, the excellent ionic conductivity of 2.94 Â 10 -4 S cm À1 and the outstanding electrocatalytic role for the redox conversion of polysulfides significantly suppress the shuttle effect, accelerate reaction kinetics, and reduce overpotential during charge/discharge process.…”
Section: Othersmentioning
confidence: 95%
“…In addition to the simple inorganic compounds, other binary inorganic or organic compounds, such as Perovskite-type structure [124][125][126], metal-organic framework (MOF) [127,128], and covalent organic framework (COF) [129], and MXene [130][131][132][133], have also been explored as effective polysulfide promoter for Li-S batteries.…”
Section: Othersmentioning
confidence: 99%
“…[3] Aiming at this issue, one of the most common approaches is to infiltrate sulfur into the porous nanostructure to mitigate LiPSs diffusion via physical confinement or chemical adsorption. [4][5][6][7][8][9][10][11][12] However, the weak trapping capability of nonpolar carbon nanostructure toward LiPSs still leads to the severe capacity decay and poor cycle life. In addition, the sluggish kinetics of Li 2 S 2 /Li 2 S nucleation brings about continuous accumulation of LiPSs in electrolytes, result-ing in large polarization and low sulfur utilization rate.…”
Section: Introductionmentioning
confidence: 99%
“…Among them, the shuttling of LiPSs between the cathode and anode is the main reason for inferior coulombic efficiency and low utilization of active materials [3] . Aiming at this issue, one of the most common approaches is to infiltrate sulfur into the porous nanostructure to mitigate LiPSs diffusion via physical confinement or chemical adsorption [4–12] . However, the weak trapping capability of nonpolar carbon nanostructure toward LiPSs still leads to the severe capacity decay and poor cycle life.…”
Section: Introductionmentioning
confidence: 99%
“…The polar inorganic materials with catalytic activity, such as metal‐based oxide/nitride/sulfide and their composites, were widely used to chemically trap LiPSs and synchronously speed up their interconversion. However, the poor electronic conductivity of these compounds leads to the sluggish redox reaction of LiPSs conversion . Hence, the metal catalyst with moderate conductivity and high polarity is highly demanded.…”
Section: Introductionmentioning
confidence: 99%