Concentration Gradient Induced Delithiation Failure of MoO3 for Li-Ion Batteries

被引:16
作者
Jang, Jihyun [1 ]
Kim, Hyun-seung [2 ]
Moon, San [3 ]
Chae, Oh B. [1 ]
Ahn, Sung-Jin [4 ]
Jung, Heechul [5 ]
Choi, Junghyun [6 ]
Oh, Seung M. [1 ]
Ryu, Ji Heon [7 ]
Yoon, Taeho [8 ]
机构
[1] Seoul Natl Univ, Dept Chem & Biol Engn, Seoul 08826, South Korea
[2] Korea Elect Technol Inst, Adv Batteries Res Ctr, Seongnam 13509, South Korea
[3] Korea Res Inst Chem Technol, Energy Mat Res Ctr, Daejeon 34114, South Korea
[4] Samsung Adv Inst Technol, Suwon 16678, South Korea
[5] Dong A Univ, Energy & Mineral Resources Engn, Busan 49315, South Korea
[6] Korea Inst Ceram Engn & Technol, Energy Storage Mat Ctr, Energy & Environm Div, Jinju 52852, South Korea
[7] Korea Polytech Univ, Grad Sch Knowledge Based Technol & Energy, Shihung 15073, South Korea
[8] Yeungnam Univ, Sch Chem Engn, Gyongsan 38541, South Korea
基金
新加坡国家研究基金会;
关键词
Li-ion batteries; transition metal oxides; molybdenum oxides; conversion reactions; concentration gradients; ELECTRODE MATERIALS; LITHIUM; INTERCALATION; REACTIVITY;
D O I
10.1021/acs.nanolett.1c04290
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electric vehicle manufacturers worldwide are demanding superior lithium-ion batteries, with high energy and power densities, compared to gasoline engines. Although conversion-type metal oxides are promising candidates for high-capacity anodes, low initial Coulombic efficiency (ICE) and poor capacity retention have hindered research on their applications. In this study, the ICE of conversion-type MoO3 is investigated, with a particular focus on the delithiation failure. A computational modeling predicts the concentration gradient of Li+ in MoO3 particles. The highly delithiated outer region of the particle forms a layer with low electronic conductivity, which impedes further delithiation. A comparative study using various sizes of MoO3 particles demonstrated that the electrode failure during delithiation is governed by the concentration gradient and the subsequent formation of a resistive shell. The proposed failure mechanism provides critical guidance for the development of conversion-type anode materials with improved electrochemical reversibility.
引用
收藏
页码:761 / 767
页数:7
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