Zhidong Ye, Yaxiong He, Huasheng Gao, Heming Hu, Tao Chen and Qi Jiang
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Experimental and theoretical results reveal that P incorporation adjusts the V d-band center, simultaneously improving LiPS chemisorption and catalyzing sulfur species conversion. This unique interfacial design facilitated bidirectional polysulfide conversion kinetics and significantly improved the nucleation and decomposition processes of Li<small><sub>2</sub></small>S. Electrochemical tests confirmed that the VP<small><sub>2</sub></small>@VS<small><sub>2</sub></small>-based cathode delivered a coulombic efficiency approaching 100% at 2C and retained a reversible capacity of 828 mAh g<small><sup>−1</sup></small> after 1000 cycles, with a minimal capacity decay rate of 0.012% per cycle. Even under a high sulfur loading of 5.5 mg cm<small><sup>−2</sup></small>, the battery exhibited exceptional cycling stability. This work proposes a novel heterointerface engineering strategy with bidirectional catalytic functionality for high-performance Li–S batteries, while offering valuable insights into interface design for other energy storage systems. Furthermore, by optimizing interfacial catalytic activity and material stability, this design significantly enhances the energy efficiency and cycling durability of batteries, thereby reducing resource consumption and environmental impact. The proposed strategy establishes a new paradigm for developing energy storage materials that combine high performance with green sustainability, advancing the practical application of clean energy technologies.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 36","pages":" 11230-11247"},"PeriodicalIF":9.2000,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"An in situ phosphorization constructed VP2@VS2 nanoflower heterostructure with a modulated d-band center of V for efficient polysulfide adsorption and conversion in lithium–sulfur batteries\",\"authors\":\"Zhidong Ye, Yaxiong He, Huasheng Gao, Heming Hu, Tao Chen and Qi Jiang\",\"doi\":\"10.1039/D5GC03028E\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Lithium–sulfur (Li–S) batteries, owing to their low cost, high theoretical energy density and environmental benignity, are regarded as one of the most promising candidates for next-generation green energy storage systems. However, their practical implementation faces significant challenges, particularly the shuttle effect of soluble lithium polysulfides (LiPSs) and the kinetic hysteresis during Li<small><sub>2</sub></small>S deposition/dissociation, which severely compromise cycling stability. To address these issues, this study employs chemical vapor deposition to <em>in situ</em> construct a VP<small><sub>2</sub></small>@VS<small><sub>2</sub></small> heterostructure with optimized interfacial characteristics on a VS<small><sub>2</sub></small> substrate. Experimental and theoretical results reveal that P incorporation adjusts the V d-band center, simultaneously improving LiPS chemisorption and catalyzing sulfur species conversion. This unique interfacial design facilitated bidirectional polysulfide conversion kinetics and significantly improved the nucleation and decomposition processes of Li<small><sub>2</sub></small>S. 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引用次数: 0
摘要
锂硫电池(li -硫电池)因其成本低、理论能量密度高、环境友好等优点,被认为是下一代绿色储能系统最有前途的候选材料之一。然而,它们的实际应用面临着重大挑战,特别是可溶性多硫化锂(LiPSs)的穿梭效应和Li2S沉积/解离过程中的动力学滞后,严重影响了循环稳定性。为了解决这些问题,本研究采用化学气相沉积技术在VS2衬底上原位构建具有优化界面特性的VP2@VS2异质结构。实验和理论结果表明,P的掺入调节了V -波段中心,同时改善了LiPS的化学吸附并催化了硫的转化。这种独特的界面设计促进了多硫化物的双向转化动力学,显著改善了Li2S的成核和分解过程。电化学测试证实,VP2@VS2-based阴极在2C下的库仑效率接近100%,在1000次循环后仍保持828 mAh g - 1的可逆容量,每循环的最小容量衰减率为0.012%。即使在5.5 mg cm−2的高硫负荷下,电池也表现出优异的循环稳定性。这项工作提出了一种具有双向催化功能的高性能Li-S电池的新型异质界面工程策略,同时为其他储能系统的界面设计提供了有价值的见解。此外,通过优化界面催化活性和材料稳定性,该设计显著提高了电池的能源效率和循环耐久性,从而减少了资源消耗和对环境的影响。提出的战略为开发将高性能与绿色可持续性相结合的储能材料建立了新的范例,推动了清洁能源技术的实际应用。
An in situ phosphorization constructed VP2@VS2 nanoflower heterostructure with a modulated d-band center of V for efficient polysulfide adsorption and conversion in lithium–sulfur batteries
Lithium–sulfur (Li–S) batteries, owing to their low cost, high theoretical energy density and environmental benignity, are regarded as one of the most promising candidates for next-generation green energy storage systems. However, their practical implementation faces significant challenges, particularly the shuttle effect of soluble lithium polysulfides (LiPSs) and the kinetic hysteresis during Li2S deposition/dissociation, which severely compromise cycling stability. To address these issues, this study employs chemical vapor deposition to in situ construct a VP2@VS2 heterostructure with optimized interfacial characteristics on a VS2 substrate. Experimental and theoretical results reveal that P incorporation adjusts the V d-band center, simultaneously improving LiPS chemisorption and catalyzing sulfur species conversion. This unique interfacial design facilitated bidirectional polysulfide conversion kinetics and significantly improved the nucleation and decomposition processes of Li2S. Electrochemical tests confirmed that the VP2@VS2-based cathode delivered a coulombic efficiency approaching 100% at 2C and retained a reversible capacity of 828 mAh g−1 after 1000 cycles, with a minimal capacity decay rate of 0.012% per cycle. Even under a high sulfur loading of 5.5 mg cm−2, the battery exhibited exceptional cycling stability. This work proposes a novel heterointerface engineering strategy with bidirectional catalytic functionality for high-performance Li–S batteries, while offering valuable insights into interface design for other energy storage systems. Furthermore, by optimizing interfacial catalytic activity and material stability, this design significantly enhances the energy efficiency and cycling durability of batteries, thereby reducing resource consumption and environmental impact. The proposed strategy establishes a new paradigm for developing energy storage materials that combine high performance with green sustainability, advancing the practical application of clean energy technologies.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.