1. School of Materials Science & Engineering, Central South University, Changsha 410083, China;2. Key Laboratory of Electronic Packaging and Advanced Functional Materials of Hunan Province, Central South University, Changsha 410083, China;3. College of Chemistry and Chemical Engineering, Jishou University, Jishou 416000, Hunan Province, China
Abstract:
Because of the advantages of high safety, environment-friendliness, affordability, and ease of processing, aqueous rechargeable zinc batteries (ARZBs) are promising candidates for next-generation large-scale energy storage systems. In recent years, various cathode materials based on vanadium/manganese/cobalt oxides, Prussian blue analogs, and organic compounds have been reported. Among them, manganese dioxide (MnO2) is widely used in ARZBs due to their outstanding advantages of low toxicity, eco-friendliness, and high capacity (616 mAh∙g−1 based on two-electron transfer). However, the diversity of the crystal structures of MnO2 and the unpredictability of the electrochemical reaction make it difficult to investigate the specific internal storage mechanism, which impedes further development of the optimal modification strategies. To date, the main recognized energy storage mechanisms are (de)intercalation and dissolution-deposition mechanisms. In the traditional (de)intercalation mechanism, the predominant issues related to MnO2 during the cycling process include Mn dissolution, irreversible phase transformation, structural collapse, and sluggish ion diffusion kinetics. On the other hand, the detailed reaction path for the dissolution-deposition mechanism, which was developed in recent years, remains controversial. In addition, the incomplete dissolution-deposition of MnO2 and the highly acidic environment inevitably leads to corrosion and hydrogen evolution of the zinc anode, as well as low Coulombic efficiency. Accordingly, optimization strategies for different reaction mechanisms have been proposed to make zinc-manganese batteries more competitive. For the (de)intercalation mechanism, modification of composite materials and nanostructure optimization strategies can be adopted to inhibit the dissolution of MnO2 and increase the number of highly active reaction sites, thus enhancing the electrochemical performance. Moreover, the guest pre-intercalation strategy can help optimize the crystal structure of MnO2, preventing the collapse of the internal structure during cycling. Besides, defect engineering and element doping strategies focus on regulating the distribution of the electronic structure for affecting the properties of MnO2, resulting in lowering the energy barrier of zinc insertion. For the dissolution-deposition mechanism, the introduction of a neutral acetate and a halide mediator can effectively facilitate the dissolution-deposition of MnO2. Meanwhile, metal element catalysis can accelerate the reaction kinetics of the MnO2 dissolution-deposition, so that high-rate performance can be achieved. Furthermore, the decoupling battery system can separate the cathodic and anodic electrolytes to restrain the hydrogen and oxygen evolution reactions and enhance the potential difference. The flow battery system can effectively eliminate the influence of concentration polarization and stabilize the ion concentration in the electrolytes, thus leading to a large capacity (> 100 mAh). Undoubtedly, MnO2 as a high-capacity, high-voltage cathode material has broad development prospects for ARZBs. Here, we systematically summarize the crystal structures and reaction mechanisms of MnO2. We also discuss the optimization strategies toward advanced MnO2 cathode materials for resolving the highlighted issues in zinc-manganese batteries, which are expected to provide research directions for the design and development of high-performance ARZBs.
