Affiliation:
1. School of Chemical and Environmental Engineering Anyang Institute of Technology Anyang 455000 P. R. China
2. Shanghai Key Laboratory of D & A for Metal‐Functional Materials School of Materials Science and Engineering Tongji University Shanghai 200092 P. R. China
3. Henan Joint International Research Laboratory of Nanocomposite Sensing Materials School of Materials Science and Engineering Anyang Institute of Technology Anyang 455000 P. R. China
Abstract
AbstractThe intrinsic low conductivity, low tap density, and huge volume expansion during lithium storage severely restrict the practicality of micron‐silicon suboxide (m‐SiOx). Here, a carbon and MXene dual confinement and dense structural engineering strategy is proposed to construct m‐SiOx composites (m‐SiOx@C/MXene) through in situ carbon coating and electrostatic self‐assembly process. This integrated structural achieves a conductivity of 157 S cm−1 for m‐SiOx@C/MXene, which is 7 and 2 orders of magnitude higher than m‐SiOx (5.3 × 10−5 S cm−1) and m‐SiOx@C (2.9 S cm−1), respectively. The tap density of m‐SiOx@C/MXene reaches 1.35 g cm−3, significantly greater than that of m‐SiOx (0.82 g cm−3) and m‐SiOx@C (0.75 g cm−3). The 29% volume expansion of m‐SiOx@C/MXene during lithium storage is much lower than the 228% and 162% of m‐SiOx and m‐SiOx@C. The synergistic effect of the above advantages enables m‐SiOx@C/MXene to exhibit excellent rate performance and cycle stability. When assembled into a full cell with the LiFePO4 (LFP) cathode, it features high capacity retention and energy density of 99.1% and 380 Wh kg−1 after 100 cycles at 0.2 C. This work provides new reference for the stable structural design of m‐SiOx or other materials with huge volume expansion during energy storage.
Funder
Chongqing Municipal Key Laboratory of Institutions of Higher Education
Natural Science Foundation of Henan Province
National Natural Science Foundation of China