阴极
三元运算
电化学
过渡金属
快离子导体
材料科学
离子
结晶学
物理化学
化学
电解质
电极
计算机科学
催化作用
有机化学
生物化学
程序设计语言
作者
Biplab Patra,Keshav Kumar,Subham Ghosh,Madhulika Mazumder,Swapan K. Pati,Premkumar Senguttuvan
标识
DOI:10.1021/acs.chemmater.3c02345
摘要
Sodium superionic conductor (NASICON)-type cathodes are considered promising candidates for long-cycle-life and high-power Na-ion batteries due to their excellent structural stability and Na-ion mobility. While their electrochemical performances have been improved by carbon-coating, particle nanosizing, and chemical tuning strategies, the fundamental understanding of the impact of chemical substitutions is still elusive, which hinders their further development. Herein, we explore a series of micron-sized NASICON-Na(9–2x–3y–4z)MnxVyZrz(PO4)3 [0 ≤ (x, y, z) ≤ 1 and (x + y + z) = 2] cathodes tailored through combinatorial chemical substitutions. Our combined structural and density functional theory studies reveal the complex evolution of (local) crystal and electronic structures, which affects electronic and Na-ion conductivities. Consequently, the Na/V-rich cathodes deliver higher capacities, cycling stabilities, and rate performances compared to those of Na/Mn-rich compositions. More specifically, the micron-sized Na3.5Mn0.75VZr0.25(PO4)3 cathode displays excellent capacity retention and rate capabilities (91.6% retention after 200 cycles and 65 mAh g–1 at 5C). This study highlights the importance of tuning the transition metal substitutions to attain high-performance NASICON cathodes.
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