Zhao Xing-He, Wu Xue-Yan, Hao Qian-Qian, Liu Yu-Si, Wang Kai-Xue, Chen Jie-Sheng
Shanghai Electrochemical Energy Devices Research Center, School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Research Center for Carbon Capture and Utilization, College of Smart Energy, Shanghai Jiao Tong University, Shanghai 200240, China.
ACS Appl Mater Interfaces. 2024 Nov 20;16(46):63647-63654. doi: 10.1021/acsami.4c15270. Epub 2024 Nov 5.
Lithium-sulfur (Li-S) batteries (LSBs) with energy density (2600 Wh/kg) much higher than typical Li-ion batteries (150-300 Wh/kg) have received considerable attention. However, the insulation nature of solid sulfur species and the high activation barrier of lithium polysulfides (LiPSs) lead to slow sulfur redox kinetics. By the introduction of catalytic materials, the effective adsorption of LiPSs, and significantly reduced conversion, energy barriers are expected to be achieved, thereby sharpening electrochemical reaction kinetics and fundamentally addressing these challenges. In this work, a multifunctional catalyst consisting of highly dispersed heterostructure Fe-FeO nanoparticles was synthesized and introduced to the LSB. Experimental and theoretical analyses revealed that the spontaneous interfacial charge redistribution, resulting in moderate polysulfide adsorption, facilitates the transfer of polysulfides and diffusion of electrons at heterogeneous interfaces. This catalyst achieves sequential catalytic processes on polysulfides with different components. Furthermore, the reduced conversion energy barriers enhanced the catalytic activity of Fe/FeO-NG for expediting LiPS conversion. Consequently, the battery exhibited long-term stability for 300 cycles with 0.03% capacity decay per cycle at 5C. This work provides in-depth insight into the fundamental design principles of effective catalysts for LSBs.
锂硫(Li-S)电池的能量密度(2600瓦时/千克)远高于典型的锂离子电池(150-300瓦时/千克),因此受到了广泛关注。然而,固态硫物种的绝缘性质和多硫化锂(LiPSs)的高活化能垒导致硫氧化还原动力学缓慢。通过引入催化材料,有望实现对LiPSs的有效吸附并显著降低转化能垒,从而加快电化学反应动力学并从根本上解决这些挑战。在这项工作中,合成了一种由高度分散的异质结构Fe-FeO纳米颗粒组成的多功能催化剂,并将其引入到锂硫电池中。实验和理论分析表明,自发的界面电荷重新分布导致适度的多硫化物吸附,促进了多硫化物在异质界面处的转移和电子扩散。这种催化剂对不同成分的多硫化物实现了连续催化过程。此外,降低的转化能垒增强了Fe/FeO-NG促进LiPS转化的催化活性。因此,该电池在5C下循环300次,容量衰减率为每循环0.03%,表现出长期稳定性。这项工作深入洞察了锂硫电池有效催化剂的基本设计原则。