Wu Heng-Liang, Huff Laura A, Esbenshade Jennifer L, Gewirth Andrew A
Department of Chemistry, University of Illinois at Urbana-Champaign , 600 S. Mathews Avenue, Urbana, Illinois 61801, United States.
ACS Appl Mater Interfaces. 2015 Sep 23;7(37):20820-8. doi: 10.1021/acsami.5b05955. Epub 2015 Sep 9.
In situ EQCM experiments were used to investigate the stability and roughness changes occurring in a sulfur-carbon cathode utilized for a Li-S battery during the charge-discharge process. Results show that the sulfur-carbon cathode gains mass during the first discharge plateau (∼2.4 V) due to the formation of the long chain polysulfides during the discharge (lithiation) process. However, further discharge to below 2.4 V yields an increase in the crystal resistance (Rc) suggesting the sulfur-carbon cathode becomes rougher. During the charge (delithiation) process, the roughness of the sulfur-carbon cathode decreases. Time dependent measurements show that the electrode surface becomes rougher with the deeper discharge, with the change occurring following a step to 1.5 V. The sulfur-carbon cathode exhibits stable Rc and frequency behavior initially, but then becomes rougher in subsequent following cycles.
采用原位电化学石英晶体微天平(EQCM)实验来研究用于锂硫电池的硫碳阴极在充放电过程中发生的稳定性和粗糙度变化。结果表明,在首次放电平台(约2.4 V)期间,硫碳阴极质量增加,这是由于在放电(锂化)过程中形成了长链多硫化物。然而,进一步放电至2.4 V以下会导致晶体电阻(Rc)增加,这表明硫碳阴极变得更粗糙。在充电(脱锂)过程中,硫碳阴极的粗糙度降低。随时间变化的测量结果表明,随着放电深度增加,电极表面变得更粗糙,这种变化在电压降至1.5 V时发生。硫碳阴极最初表现出稳定的Rc和频率行为,但在随后的循环中变得更粗糙。