Yu Xinxin, Wu Zhuangzhuang, Zhao Yuzhen, Wang Weina, Li Yongpeng, Sui Zhuyin, Xiao Juanxiu, Tian Xinlong, Chen Qi
State Key Laboratory of Marine Resource Utilization in South China Sea, School of Marine Science and Engineering, Hainan University, Haikou 570228, PR China.
School of Chemistry & Chemical Engineering, Yantai University, Yantai 264005, PR China.
J Colloid Interface Sci. 2024 May 15;662:333-341. doi: 10.1016/j.jcis.2024.02.029. Epub 2024 Feb 7.
It is significant to tailor multifunctional electrode materials for storing sustainable energy in lithium-sulfur (Li-S) batteries and converting intermittent solar energy into H, facilitated by electricity. In this context, COF-1@CNT obtained through interfacial interaction fulfilled both requisites via post-functionalization. Upon integrating COF-1@CNT with S as the cathode for Li-S batteries, the system exhibited an initial discharge capacity of 1360 mAh g. Subsequently, it maintained a sustained actual capacity even after undergoing 200 charge-discharge cycles at 0.5C. The performance improvement was attributed to the optimized conductivity due to the addition of carbon nanotubes (CNTs). Furthermore, the synergistic interaction between the nitrogen of COF-1 and lithium mitigated the shuttle effect in Li-S batteries. In the modified three-electrode electrolytic cell system, COF-1@CNT-Ru produced by COF-1@CNT with RuCl showed better electrochemical reactivity for photothermal-assisted hydrogen evolution reaction (HER). This effect was demonstrated by reducing the overpotential to 140 mV relative to the no-photothermal condition (180 mV) at a current density of 10 mA cm. This study marked the first simultaneous application of covalent organic frameworks (COFs) based materials in Li-S batteries and photothermal-assisted electrocatalysts. The modified electrocatalytic system held promise as a novel avenue for exploring solar thermal energy utilization.
定制多功能电极材料对于在锂硫(Li-S)电池中存储可持续能源以及借助电力将间歇性太阳能转化为氢气而言具有重要意义。在此背景下,通过界面相互作用获得的COF-1@CNT通过后功能化满足了这两个要求。将COF-1@CNT与硫整合作为Li-S电池的阴极时,该系统的初始放电容量为1360 mAh g。随后,即使在0.5C下经历200次充放电循环后,它仍保持持续的实际容量。性能的提升归因于添加碳纳米管(CNT)后优化的导电性。此外,COF-1中的氮与锂之间的协同相互作用减轻了Li-S电池中的穿梭效应。在改进的三电极电解池系统中,由COF-1@CNT与RuCl制备的COF-1@CNT-Ru对光热辅助析氢反应(HER)表现出更好的电化学反应活性。在电流密度为10 mA cm时,相对于无光热条件(180 mV),过电位降低至140 mV,证明了这种效果。这项研究标志着基于共价有机框架(COF)的材料首次同时应用于Li-S电池和光热辅助电催化剂。改进后的电催化系统有望成为探索太阳能热利用的新途径。