过电位
化学
碳纳米管
电催化剂
共价有机骨架
锂(药物)
共价键
光热治疗
纳米技术
阴极
化学工程
背景(考古学)
有机化学
电化学
材料科学
电极
物理化学
古生物学
内分泌学
工程类
生物
医学
作者
Xinxin Yu,Zhuangzhuang Wu,Yuzhen Zhao,Weina Wang,Yongpeng Li,Zhuyin Sui,Juanxiu Xiao,Xinlong Tian,Qi Chen
标识
DOI:10.1016/j.jcis.2024.02.029
摘要
It is significant to tailor multifunctional electrode materials for storing sustainable energy in lithium-sulfur (Li-S) batteries and converting intermittent solar energy into H2, 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−1. 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 RuCl3 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−2. 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.
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