Reviving Cost‐Effective Organic Cathodes in Halide‐Based All‐Solid‐State Lithium Batteries
Yingjie Gao, Jiamin Fu, Yang Hu, Feipeng Zhao, W.S. Li, Sixu Deng, Yipeng Sun, Xiaoge Hao, Jinjin Ma, Xiaoting Lin, Changhong Wang, Ruying Li, Xueliang Sun
Abstract
Abstract The evolution of inorganic solid electrolytes has revolutionized the field of sustainable organic cathode materials, particularly by addressing the dissolution problems in traditional liquid electrolytes. However, current sulfide‐based all‐solid‐state lithium‐organic batteries still face challenges such as high working temperatures, high costs, and low voltages. Here, we design an all‐solid‐state lithium battery based on a cost‐effective organic cathode material phenanthrenequinone (PQ) and a halide solid electrolyte Li 2 ZrCl 6 . Thanks to the good compatibility between PQ and Li 2 ZrCl 6 , the PQ cathode achieved a high specific capacity of 248 mAh g −1 (96 % of the theoretical capacity), a high average discharge voltage of 2.74 V (vs. Li + /Li), and a good capacity retention of 95 % after 100 cycles at room temperature (25 °C). Furthermore, the interactions between the high‐voltage carbonyl PQ cathode and both sulfide and halide solid electrolytes, as well as the redox mechanism of the PQ cathode in all‐solid‐state batteries, were carefully studied by a variety of advanced characterizations. We believe such a design and the corresponding investigations into the underlying chemistry give insights for the further development of practical all‐solid‐state lithium‐organic batteries.