Slesinska Sylwia, Réty Bénédicte, Matei-Ghimbeu Camélia, Fic Krzysztof, Menzel Jakub
Institute of Chemistry and Technical Electrochemistry, Poznan University of Technology, Berdychowo 4, 60-965 Poznan, Poland.
Institut de Science des Matériaux de Mulhouse (IS2M), Université de Haute-Alsace, CNRS UMR 7361, F-68100 Mulhouse, France.
ACS Appl Energy Mater. 2025 Jan 10;8(2):810-820. doi: 10.1021/acsaem.4c01940. eCollection 2025 Jan 27.
This paper reports on several mechanisms of carbon aging in a hybrid lithium-ion capacitor operating with 1 mol L LiPF in an ethylene carbonate/dimethyl carbonate 1:1 vol/vol electrolyte. Carbon electrodes were subjected to a constant polarization protocol (i.e., floating) at various voltages and analyzed postmortem via several complementary techniques. The selected protocol was able to simulate the behavior of the real system. Due to the use of metallic lithium as the counter electrode, the influence of battery-like aging mechanisms was assumed to be limited. Our approach focused on the aging mechanisms related to the carbon electrode and determined the structural and chemical changes leading to energy fading in lithium-ion hybrid capacitors. It was shown that an increase in applied voltage not only results in faster system degradation but directs the aging chemistry to different pathways: at moderate voltage values, both capacitance loss and simultaneous increase in resistance predominate. This could be associated with the decrease in carbon surface area and possible pore clogging with by-products of electrolyte degradation and carbon oxidation disrupting the C sp network. When high voltage is applied, further oxidation of carbon occurs with an increase in measured resistance that leads to the relevant end-of-life criterion to be reached. Detailed postmortem analysis results attributed it to the formation of phenol and ether groups together with electrolyte decomposition products, higher oxidation levels, and structure degradation. It was evidenced that the decrease in the overall carbon conductivity and, in certain cases, modification of the textural properties ultimately aggravates the capacitor performance.
本文报道了在以碳酸乙烯酯/碳酸二甲酯1:1体积比为电解液、1 mol/L LiPF运行的混合锂离子电容器中碳老化的几种机制。碳电极在不同电压下进行恒极化程序(即浮充),并通过几种互补技术进行死后分析。所选程序能够模拟实际系统的行为。由于使用金属锂作为对电极,电池类老化机制的影响被认为是有限的。我们的方法侧重于与碳电极相关的老化机制,并确定导致锂离子混合电容器能量衰减的结构和化学变化。结果表明,施加电压的增加不仅会导致系统更快地退化,还会使老化化学过程转向不同的途径:在中等电压值下,电容损失和电阻同时增加占主导地位。这可能与碳表面积的减小以及电解质降解和碳氧化的副产物可能堵塞孔隙从而破坏C sp网络有关。当施加高电压时,碳会进一步氧化,测量电阻增加,导致达到相关的寿命终止标准。详细的死后分析结果将其归因于酚类和醚类基团的形成以及电解质分解产物、更高的氧化水平和结构降解。有证据表明,整体碳电导率的降低以及在某些情况下结构性质的改变最终会加剧电容器的性能