Solid-State Reaction Heterogeneity During Calcination of Lithium-Ion Battery Cathode

被引:28
|
作者
Jo, Sugeun [1 ]
Han, Jeongwoo [1 ]
Seo, Sungjae [1 ]
Kwon, Oh-Sung [2 ]
Choi, Subin [1 ]
Zhang, Jin [3 ]
Hyun, Hyejeong [1 ]
Oh, Juhyun [1 ,4 ,5 ]
Kim, Juwon [1 ]
Chung, Jinkyu [1 ]
Kim, Hwiho [1 ]
Wang, Jian [6 ]
Bae, Junho [1 ]
Moon, Junyeob [1 ]
Park, Yoon-Cheol [7 ]
Hong, Moon-Hi [7 ]
Kim, Miyoung [4 ,5 ]
Liu, Yijin [3 ]
Sohn, Il [2 ]
Jung, Keeyoung [7 ]
Lim, Jongwoo [1 ]
机构
[1] Seoul Natl Univ, Dept Chem, 1 Gwanak Ro, Seoul 08826, Seoul, South Korea
[2] Yonsei Univ, Dept Mat Sci & Engn, Seoul 120749, South Korea
[3] SLAC Natl Accelerator Lab, Stanford Synchrot Radiat Lightsource, Menlo Pk, CA 94025 USA
[4] Seoul Natl Univ, Res Inst Adv Mat RIAM, Dept Mat Sci & Engn, 1 Gwanak-ro, Seoul 08826, South Korea
[5] Seoul Natl University, Res Inst Adv Mat RIAM, 1 Gwanak Ro, Seoul 08826, South Korea
[6] City Univ Hong Kong, Sch Energy & Environm, Hong Kong, Peoples R China
[7] Res Inst Ind Sci & Technol RIST, Mat Res Div, Pohang 37673, South Korea
基金
新加坡国家研究基金会;
关键词
Li-ion batteries; nickel-rich cathodes; phase transitions with solid-state reaction; spatial distribution of local chemical compositions within the particles; synthesis during calcination; THERMAL-STABILITY; OXIDE; LIXNI1-XO; SURFACE; CHARGE; MN; INTERCALATION; HYDROXIDES; MECHANISM; KINETICS;
D O I
10.1002/adma.202207076
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
During solid-state calcination, with increasing temperature, materials undergo complex phase transitions with heterogeneous solid-state reactions and mass transport. Precise control of the calcination chemistry is therefore crucial for synthesizing state-of-the-art Ni-rich layered oxides (LiNi1-x-yCoxMnyO2, NRNCM) as cathode materials for lithium-ion batteries. Although the battery performance depends on the chemical heterogeneity during NRNCM calcination, it has not yet been elucidated. Herein, through synchrotron-based X-ray, mass spectrometry microscopy, and structural analyses, it is revealed that the temperature-dependent reaction kinetics, the diffusivity of solid-state lithium sources, and the ambient oxygen control the local chemical compositions of the reaction intermediates within a calcined particle. Additionally, it is found that the variations in the reducing power of the transition metals (i.e., Ni, Co, and Mn) determine the local structures at the nanoscale. The investigation of the reaction mechanism via imaging analysis provides valuable information for tuning the calcination chemistry and developing high-energy/power density lithium-ion batteries.
引用
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页数:13
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