State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University , Shanghai 200433, China.
Sustainable Energy Technologies Center, College of Engineering, King Saud University , Riyadh 11421, Kingdom of Saudi Arabia.
ACS Appl Mater Interfaces. 2017 May 10;9(18):15549-15556. doi: 10.1021/acsami.7b03687. Epub 2017 Apr 26.
Polymer cathode materials are promising alternatives to inorganic counterparts for both lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) due to their high theoretical capacity, adjustable molecular structure, and strong adaptability to different counterions in batteries, etc. However, they suffer from poor practical capacity and low rate capability because of their intrinsically poor conductivity. Herein, we report the synthesis of self-assembled graphene/poly(anthraquinonyl sufide) (PAQS) composite aerogel (GPA) with efficient integration of a three-dimensional (3D) graphene framework with electroactive PAQS particles via a novel dispersion-assembly strategy which can be used as a free-standing flexible cathode upon mechanical pressing. The entire GPA cathode can deliver the highest capacity of 156 mAh g at 0.1 C (1 C = 225 mAh g) with an ultrahigh utilization (94.9%) of PAQS and exhibits an excellent rate performance with 102 mAh g at 20 C in LIBs. Furthermore, the flexible GPA film was also tested as cathode for SIBs and demonstrated a high-rate capability with 72 mAh g at 5 C and an ultralong cycling stability (71.4% capacity retention after 1000 cycles at 0.5 C) which has rarely been achieved before. Such excellent electrochemical performance of GPA as cathode for both LIBs and SIBs could be ascribed to the fast redox kinetics and electron transportation within GPA, resulting from the interconnected conductive framework of graphene and the intimate interaction between graphene and PAQS through an efficient wrapping structure. This approach opens a universal way to develop cathode materials for powerful batteries with different metal-based counter electrodes.
高分子阴极材料由于其高理论容量、可调分子结构以及对电池中不同反离子的强适应性等优点,是锂离子电池(LIBs)和钠离子电池(SIBs)无机对应物的有前途的替代品。然而,由于其本身导电性差,它们的实际容量差且倍率性能低。在此,我们报告了通过一种新颖的分散-组装策略合成自组装的石墨烯/聚(蒽醌基硫化物)(PAQS)复合气凝胶(GPA),该策略可以有效地将具有三维(3D)石墨烯框架与电活性 PAQS 颗粒集成在一起,并且可以在机械压力下用作独立的柔性阴极。整个 GPA 阴极在 0.1 C(1 C = 225 mAh g)下可提供最高 156 mAh g 的容量,PAQS 的超高利用率(94.9%),并且在 LIBs 中具有出色的倍率性能,在 20 C 时可提供 102 mAh g 的容量。此外,柔性 GPA 薄膜也被测试为 SIBs 的阴极,并表现出高倍率性能,在 5 C 时具有 72 mAh g 的容量,在 0.5 C 时经过 1000 次循环后具有 71.4%的容量保持率,这在以前很少见。GPA 作为 LIBs 和 SIBs 的阴极的这种优异的电化学性能可归因于 GPA 内快速的氧化还原动力学和电子输运,这是由于石墨烯的互连导电框架和石墨烯与 PAQS 之间通过有效的包裹结构的紧密相互作用。这种方法为具有不同金属基对电极的强大电池开发阴极材料开辟了一条通用途径。