Wang Mingli, Zhang Hong, Zhang Wenli, Chen Qianwang, Lu Ke
Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Anhui Graphene Engineering Laboratory, Anhui University, Hefei, Anhui, 230601, P. R. China.
Hefei National Laboratory for Physical Science at Microscale, Hefei, Anhui, 230026, P. R. China.
Small Methods. 2022 Jul;6(7):e2200335. doi: 10.1002/smtd.202200335. Epub 2022 May 12.
Benefiting from the merits of natural abundance, low cost, and ultrahigh theoretical energy density, the room temperature sodium-sulfur (RT NaS) batteries are regarded as one of the promising candidates for the next-generation scalable energy storage devices. However, the uncontrollable sulfur speciation pathways severely hinder its practical applications. Recently, various strategies have been employed to tune the conversion pathways of sulfur, such as physical confinement, chemical inhibition, and electrocatalysis. Herein, the recent advances in electrocatalytic effects manipulate sulfur speciation pathways in advanced RT NaS electrochemistry are reviewed, including the promotion of the nearly full conversion of long-chain polysulfides, short-chain polysulfides, and small sulfur molecules. The underlying catalytic modulation mechanism that fundamentally tunes the electrochemical pathway of sulfur species is comprehensively summarized along with the design strategies for catalytic active centers. Furthermore, the challenge and potential solutions to realize the quasi-solid conversion of sulfur are proposed to accelerate the real application of RT NaS batteries.
得益于天然丰度高、成本低以及超高理论能量密度等优点,室温钠硫(RT NaS)电池被视为下一代可扩展储能设备的有前景的候选者之一。然而,不可控的硫形态转化途径严重阻碍了其实际应用。最近,人们采用了各种策略来调节硫的转化途径,如物理限制、化学抑制和电催化。在此,综述了电催化效应在先进的RT NaS电化学中操纵硫形态转化途径的最新进展,包括促进长链多硫化物、短链多硫化物和小分子硫的近乎完全转化。从根本上调节硫物种电化学途径的潜在催化调制机制以及催化活性中心的设计策略被全面总结。此外,还提出了实现硫的准固态转化的挑战和潜在解决方案,以加速RT NaS电池的实际应用。