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

被引:7
|
作者
Jha, Pawan Kumar [1 ]
Totade, Sanyam Nitin [2 ]
Barpanda, Prabeer [1 ,3 ,4 ]
Sai Gautam, Gopalakrishnan [2 ]
机构
[1] Indian Inst Sci, Mat Res Ctr, Faraday Mat Lab FaMaL, Bangalore 560012, India
[2] Indian Inst Sci, Dept Mat Engn, Bengaluru 560012, Karnataka, India
[3] Helmholtz Inst Ulm HIU, Electrochem Energy Storage, D-89081 Ulm, Germany
[4] Karlsruhe Inst Technol KIT, Inst Nanotechnol, D-76021 Karlsruhe, Germany
关键词
TOTAL-ENERGY CALCULATIONS; TRANSITION-METAL OXIDE; X LESS-THAN; AB-INITIO; SOLID-SOLUTION; INTERCALATION; EVOLUTION; STORAGE; DESIGN; PHASES;
D O I
10.1021/acs.inorgchem.3c01686
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
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.
引用
收藏
页码:14971 / 14979
页数:9
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