Physikalisch-Chemisches Institut, Justus-Liebig-Universität Giessen , Heinrich-Buff-Ring 17, 35392 Giessen, Germany.
Center for Materials Research, Justus Liebig University Giessen , Heinrich-Buff-Ring 16, 35392 Giessen, Germany.
ACS Appl Mater Interfaces. 2017 Oct 18;9(41):35888-35896. doi: 10.1021/acsami.7b11530. Epub 2017 Oct 3.
All-solid-state batteries (SSBs) have recently attracted much attention due to their potential application in electric vehicles. One key issue that is central to improve the function of SSBs is to gain a better understanding of the interfaces between the material components toward enhancing the electrochemical performance. In this work, the interfacial properties of a carbon-containing cathode composite, employing LiGePS as the solid electrolyte, are investigated. A large interfacial charge-transfer resistance builds up upon the inclusion of carbon in the composite, which is detrimental to the resulting cycle life. Analysis by X-ray photoelectron spectroscopy reveals that carbon facilitates faster electrochemical decomposition of the thiophosphate solid electrolyte at the cathode/solid electrolyte interface-by transferring the low chemical potential of lithium in the charged state deeper into the solid electrolyte and extending the decomposition region. The occurring accumulation of highly oxidized sulfur species at the interface is likely responsible for the large interfacial resistances and aggravated capacity fading observed.
全固态电池(SSBs)由于在电动汽车中的潜在应用而受到了广泛关注。提高 SSBs 性能的一个关键问题是更好地理解材料组件之间的界面,以提高电化学性能。在这项工作中,研究了采用 LiGePS 作为固体电解质的含碳正极复合材料的界面特性。在复合材料中加入碳会导致界面电荷转移电阻显著增大,从而对循环寿命产生不利影响。X 射线光电子能谱分析表明,碳通过将充电态下锂的低化学势更深地转移到固体电解质中,并扩展其分解区域,促进了硫代磷酸盐固体电解质在正极/固体电解质界面处的电化学更快分解。界面处高度氧化的硫物种的积累很可能是导致观察到的大界面电阻和加剧的容量衰减的原因。