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New insights into the modification mechanism of Li-rich Li1.2Mn0.6Ni0.2O2 coated by Li2ZrO3

Lithium-rich Mn-based layered cathode materials have attracted wide attention due to their high specific capacity for lithium-ion batteries. However, some critical issues i.e. poor rate capability and voltage fade have limited their practical applications. Herein, we propose a synchronous lithiation...

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Published in:Physical chemistry chemical physics : PCCP 2016-05, Vol.18 (19), p.13322-13331
Main Authors: Zhang, Jicheng, Zhang, Heng, Gao, Rui, Li, Zhengyao, Hu, Zhongbo, Liu, Xiangfeng
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Zhang, Heng
Gao, Rui
Li, Zhengyao
Hu, Zhongbo
Liu, Xiangfeng
description Lithium-rich Mn-based layered cathode materials have attracted wide attention due to their high specific capacity for lithium-ion batteries. However, some critical issues i.e. poor rate capability and voltage fade have limited their practical applications. Herein, we propose a synchronous lithiation strategy to coat Li-rich Li 1.2 Mn 0.6 Ni 0.2 O 2 (LMNO) with a thin layer of Li + -conductive Li 2 ZrO 3 . The obtained syn-Li 2 ZrO 3 @LMNO integrates the advantages of the Li 2 ZrO 3 coating and Zr 4+ doping, and shows a much higher rate capability and cycling stability than those of the counterpart post-Li 2 ZrO 3 @LMNO fabricated by a post-coating method. More importantly, the average voltage of syn-Li 2 ZrO 3 @LMNO has been enhanced by 0.15 V and the voltage decay has also been mitigated. New insights into the synergetic modification mechanism of the Li 2 ZrO 3 coating and Zr 4+ doping have been proposed. The coating layer of Li + -conductive Li 2 ZrO 3 alleviates the surface side reactions, suppresses the transition metal dissolution and enhances the Li-ion conductivity. Meanwhile, the doping and incorporation of Zr 4+ into the host structure accompanied by the Li 2 ZrO 3 coating expands the interplanar spacing and decreases Li/Ni mixing which facilitates Li + diffusion. In addition, the integration of the Li 2 ZrO 3 coating and Zr 4+ doping also further enhances the layered structure stability and mitigates the voltage fade during lithiation/delithiation cycles. Moreover, the proposed synchronous lithiation coating route avoids the duplicated high-temperature calcinations and can also be widely used to modify some other cathode materials. The synergetic modification mechanism in Li 2 ZrO 3 -coated Li-rich Li 1.2 Mn 0.6 Ni 0.2 O 2 via a synchronous lithiation strategy has been proposed.
doi_str_mv 10.1039/c6cp01366j
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However, some critical issues i.e. poor rate capability and voltage fade have limited their practical applications. Herein, we propose a synchronous lithiation strategy to coat Li-rich Li 1.2 Mn 0.6 Ni 0.2 O 2 (LMNO) with a thin layer of Li + -conductive Li 2 ZrO 3 . The obtained syn-Li 2 ZrO 3 @LMNO integrates the advantages of the Li 2 ZrO 3 coating and Zr 4+ doping, and shows a much higher rate capability and cycling stability than those of the counterpart post-Li 2 ZrO 3 @LMNO fabricated by a post-coating method. More importantly, the average voltage of syn-Li 2 ZrO 3 @LMNO has been enhanced by 0.15 V and the voltage decay has also been mitigated. New insights into the synergetic modification mechanism of the Li 2 ZrO 3 coating and Zr 4+ doping have been proposed. The coating layer of Li + -conductive Li 2 ZrO 3 alleviates the surface side reactions, suppresses the transition metal dissolution and enhances the Li-ion conductivity. Meanwhile, the doping and incorporation of Zr 4+ into the host structure accompanied by the Li 2 ZrO 3 coating expands the interplanar spacing and decreases Li/Ni mixing which facilitates Li + diffusion. In addition, the integration of the Li 2 ZrO 3 coating and Zr 4+ doping also further enhances the layered structure stability and mitigates the voltage fade during lithiation/delithiation cycles. Moreover, the proposed synchronous lithiation coating route avoids the duplicated high-temperature calcinations and can also be widely used to modify some other cathode materials. 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title New insights into the modification mechanism of Li-rich Li1.2Mn0.6Ni0.2O2 coated by Li2ZrO3
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