Evaluation of P3-Type Layered Oxides as K-Ion Battery Cathodes

化学 电化学 密度泛函理论 插层(化学) 过渡金属 八面体 电池(电) 阴极 离子 电压 蜂巢 结构稳定性 硅烯 电极 计算化学 无机化学 物理化学 热力学 几何学 生物化学 功率(物理) 物理 有机化学 量子力学 数学 结构工程 工程类 催化作用
作者
Pawan Kumar Jha,Sanyam Nitin Totade,Prabeer Barpanda,Gopalakrishnan Sai Gautam
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:62 (37): 14971-14979
标识
DOI:10.1021/acs.inorgchem.3c01686
摘要

Given the increasing energy storage demands and limited natural resources of Li, K-ion batteries (KIBs) could be promising next-generation systems having natural abundance, similar chemistry, and energy density. Here, we have investigated the P3-type K0.5TMO2 (where TM = Ti, V, Cr, Mn, Co, or Ni) systems using density functional theory calculations as potential positive intercalation electrodes (or cathodes) for KIBs. Specifically, we have identified ground-state configurations and calculated the average topotactic voltages, electronic structures, on-site magnetic moments, and thermodynamic stabilities of all P3-K0.5TMO2 compositions and their corresponding depotassiated P3-TMO2 frameworks. Additionally, we evaluated the dynamic stability and K-mobility in select P3 structures. We find that K adopts the honeycomb or zig-zag configuration within each K-layer of all P3 structures considered, irrespective of the transition-metal (TM). In terms of voltages, we find the Co- and Ti-based compositions to exhibit the highest (4.59 V vs. K) and lowest (2.24 V) voltages, respectively, with the TM contributing to the redox behavior upon K (de-)intercalation. We observe all P3-K0.5TMO2 to be (meta)stable and hence experimentally synthesizable according to our 0 K convex hull calculations, while all depotassiated P3-TMO2 configurations are unstable and may appear during electrochemical cycling. Also, we verified the stability of the prismatic coordination environment of K compared to octahedral coordination at the K0.5TMO2 compositions using Rouxel and cationic potential models. Finally, combining our voltage and stability calculations, we find P3-KxCoO2 to be the most promising cathode composition, while P3-KxNiO2 is worth exploring. We also find P3-KxMnO2 to be worth pursuing given its dynamic stability and facile migration of K+ at both potassiated and depotassiated compositions. Our work should contribute to the exploration of strategies and materials required to make practical KIBs.
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