Wang Yuhan, Zhong Jinze, Liu Siqi, Chen Jinyan, Hou Jianhua, Duan Qian
School of Materials Science and Engineering, Changchun University of Science and Technology, Changchun 130022, P. R. China.
Engineering Research Center of Optoelectronic Functional Materials, Ministry of Education, Changchun 130022, P. R. China.
ACS Appl Mater Interfaces. 2025 Jul 2;17(26):38731-38743. doi: 10.1021/acsami.5c06874. Epub 2025 Jun 16.
The sluggish conversion kinetics of lithium polysulfide (LiPSs) and the notorious shuttle effect caused by the dissolution of highly soluble LiPSs in the electrolyte have become major obstacles to the practical application of lithium-sulfur batteries. Thus, searching for bifunctional catalyst materials that can effectively capture and convert LiPSs to inhibit their shuttling effect has become the key to developing efficient lithium-sulfur batteries. In this paper, the potential of a series of doped VS monolayers with nonmetallic atoms replacing S atoms as cathode catalytic materials for lithium-sulfur batteries is discussed through first-principles calculations. The nonmetallic doping system focused herein exhibits unique structural stability and intrinsic conductivity advantages compared to conventional metal doping strategies that may induce problems such as lattice distortion. The study results show that among a series of nonmetallic atoms doped VS monolayers, O-VS and Se-VS were considered the best candidates. The adsorption strength of soluble LiPSs on both the top and bottom surfaces of O-VS and Se-VS was sufficient to inhibit the shuttle effect, while the structure of LiPSs remained unchanged. This was necessary to decrease the capacity decay. The projected density of states (PDOS) calculation indicates that O-VS and Se-VS maintain the metallic properties of VS, even after the adsorption of LiPSs. Importantly, O-VS and Se-VS exhibit significant catalytic activity for sulfur reduction reactions (SRR) during discharge and for the decomposition of LiS during charging. The suitable d and p band center positions and the more charge accumulation by adsorbed LiPSs are responsible for the high redox kinetics of O-VS catalyzed polysulfide conversion. Furthermore, the energy barrier for Li ions diffusion on the Se-VS surface is smaller than that on the VS, and the energy barrier for diffusion on the O-VS surface is smaller than that on the graphene surface, which facilitates Li ions diffusion on the surface. Overall, O-VS and Se-VS can be considered an effective catalyst with strong adsorption behavior, enhanced electronic conductivity, and improved redox kinetics of polysulfides. This study provides new insights for the further development of high-performance lithium-sulfur batteries.
多硫化锂(LiPSs)缓慢的转化动力学以及高溶解性的LiPSs在电解液中溶解所导致的臭名昭著的穿梭效应,已成为锂硫电池实际应用的主要障碍。因此,寻找能够有效捕获和转化LiPSs以抑制其穿梭效应的双功能催化剂材料,已成为开发高效锂硫电池的关键。本文通过第一性原理计算,探讨了一系列用非金属原子取代S原子的掺杂VS单层作为锂硫电池阴极催化材料的潜力。与可能引发诸如晶格畸变等问题的传统金属掺杂策略相比,本文所关注的非金属掺杂体系展现出独特的结构稳定性和本征导电性优势。研究结果表明,在一系列非金属原子掺杂的VS单层中,O-VS和Se-VS被认为是最佳候选材料。可溶性LiPSs在O-VS和Se-VS的顶面和底面的吸附强度足以抑制穿梭效应,同时LiPSs的结构保持不变。这对于降低容量衰减是必要的。态密度投影(PDOS)计算表明,即使在吸附LiPSs之后,O-VS和Se-VS仍保持VS的金属特性。重要的是,O-VS和Se-VS在放电过程中对硫还原反应(SRR)以及充电过程中对LiS的分解表现出显著的催化活性。合适的d和p带中心位置以及被吸附的LiPSs积累的更多电荷,是O-VS催化多硫化物转化的高氧化还原动力学的原因。此外,锂离子在Se-VS表面扩散的能垒小于在VS表面的能垒,在O-VS表面扩散的能垒小于在石墨烯表面的能垒,这有利于锂离子在表面扩散。总体而言,O-VS和Se-VS可被视为具有强吸附行为、增强的电子导电性以及改善的多硫化物氧化还原动力学的有效催化剂。本研究为高性能锂硫电池的进一步发展提供了新的见解。