Sun Tianjiang, Zhang Weijia, Nian Qingshun, Tao Zhanliang
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), College of Chemistry, Haihe Laboratory of Sustainable Chemical Transformations, Renewable Energy Conversion and Storage Center, Nankai University, Tianjin, 300071, People's Republic of China.
CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, Hefei National Laboratory for Physical Science at the Microscale, University of Science and Technology of China Hefei, Hefei, 230026, Anhui, People's Republic of China.
Nanomicro Lett. 2023 Jan 13;15(1):36. doi: 10.1007/s40820-022-01009-x.
Novel small sulfur heterocyclic quinones (6a,16a-dihydrobenzo[b]naphtho[2',3':5,6][1,4]dithiino[2,3-i]thianthrene-5,7,9,14,16,18-hexaone (4S6Q) and benzo[b]naphtho[2',3':5,6][1,4]dithiino[2,3-i]thianthrene-5,9,14,18-tetraone (4S4Q)) are developed by molecule structural design method and as cathode for aqueous zinc-organic batteries. The conjugated thioether (-S-) bonds as connected units not only improve the conductivity of compounds but also inhibit their dissolution by both extended π-conjugated plane and constructed flexible molecular skeleton. Hence, the Zn//4S6Q and Zn//4S4Q batteries exhibit satisfactory electrochemical performance based on 3.5 mol L (M) Zn(ClO) electrolyte. For instance, the Zn//4S6Q battery obtains 240 and 208.6 mAh g of discharge capacity at 150 mA g and 30 A g, respectively. The excellent rate capability is ascribed to the fast reaction kinetics. This system displays a superlong life of 20,000 cycles with no capacity fading at 3 A g. Additionally, the H-storage mechanism of the 4S6Q compound is demonstrated by ex situ analyses and density functional theory calculations. Impressively, the battery can normally work at - 60 °C benefiting from the anti-freezing electrolyte and maintain a high discharge capacity of 201.7 mAh g, which is 86.2% of discharge capacity at 25 °C. The cutting-edge electrochemical performances of these novel compounds make them alternative electrode materials for Zn-organic batteries.
通过分子结构设计方法开发了新型小硫杂环醌(6a,16a-二氢苯并[b]萘并[2',3':5,6][1,4]二硫代并[2,3-i]噻蒽-5,7,9,14,16,18-六酮(4S6Q)和苯并[b]萘并[2',3':5,6][1,4]二硫代并[2,3-i]噻蒽-5,9,14,18-四酮(4S4Q)),并将其用作水系锌有机电池的阴极。作为连接单元的共轭硫醚(-S-)键不仅提高了化合物的导电性,还通过扩展的π共轭平面和构建的柔性分子骨架抑制了它们的溶解。因此,基于3.5 mol L(M)Zn(ClO)电解液的Zn//4S6Q和Zn//4S4Q电池表现出令人满意的电化学性能。例如,Zn//4S6Q电池在150 mA g和30 A g下的放电容量分别为240和208.6 mAh g。优异的倍率性能归因于快速的反应动力学。该体系在3 A g下具有20000次循环的超长寿命且无容量衰减。此外,通过非原位分析和密度泛函理论计算证明了4S6Q化合物的储氢机理。令人印象深刻的是,受益于抗冻电解液,该电池在-60°C时仍能正常工作,并保持201.7 mAh g的高放电容量,这是25°C时放电容量的86.2%。这些新型化合物的前沿电化学性能使其成为锌有机电池的替代电极材料。