TY - JOUR
T1 - Mesoporous N-rich carbon nanospheres regulating high dispersion of red phosphorus for sodium-ion batteries
AU - Zhang, Hongyi
AU - Li, Wenda
AU - Luo, Hao
AU - Huang, Lingyan
AU - Wei, Facai
AU - Ke, Shanzhe
AU - Ma, Liguo
AU - Jing, Chengbin
AU - Cheng, Jiangong
AU - Liu, Shaohua
N1 - Publisher Copyright:
© 2025
PY - 2026/2
Y1 - 2026/2
N2 - The intrinsic insulation and drastic volume change of the red phosphorus during the 3-electron alloying process greatly limits its widespread applications in sodium-ion batteries. Here, we report a monomicelle-directed assembly approach for controllable synthesis of monodispersed mesoporous polypyrrole (PPy) nanospheres, which allows for the shape-preserving conversion into N-doped carbon with regular mesoscopic pore and high surface area, thus affording a high dispersion of red phosphorus during melt impregnation process due to the available diffusion apertures and strong molecular chemical anchoring. Moreover, the theoretical calculations further revealed that positively polarized pyridine N atoms in N-doped mesoporous carbon nanospheres can empower comprehensive regulation of red phosphorus adsorption by strong chemical binding. Benefitting from the above advantages, the resultant red phosphorus host for sodium-ion batteries delivered an outstanding reversible capacity of 856 mAh/g with a capacity fading rate of only 0.025 % per cycle during 1000 cycles at 1.0 A/g. This work provides an effective approach based on monomicelle-directed assembly engineering of carbon-based phosphorus hosts for advanced energy conversion and storage systems.
AB - The intrinsic insulation and drastic volume change of the red phosphorus during the 3-electron alloying process greatly limits its widespread applications in sodium-ion batteries. Here, we report a monomicelle-directed assembly approach for controllable synthesis of monodispersed mesoporous polypyrrole (PPy) nanospheres, which allows for the shape-preserving conversion into N-doped carbon with regular mesoscopic pore and high surface area, thus affording a high dispersion of red phosphorus during melt impregnation process due to the available diffusion apertures and strong molecular chemical anchoring. Moreover, the theoretical calculations further revealed that positively polarized pyridine N atoms in N-doped mesoporous carbon nanospheres can empower comprehensive regulation of red phosphorus adsorption by strong chemical binding. Benefitting from the above advantages, the resultant red phosphorus host for sodium-ion batteries delivered an outstanding reversible capacity of 856 mAh/g with a capacity fading rate of only 0.025 % per cycle during 1000 cycles at 1.0 A/g. This work provides an effective approach based on monomicelle-directed assembly engineering of carbon-based phosphorus hosts for advanced energy conversion and storage systems.
KW - Mesoporous materials
KW - Monomicelle-directed assembly
KW - N-doped carbon nanospheres
KW - Phosphorus hosts
KW - Sodium-ion batteries
UR - https://www.scopus.com/pages/publications/105022691258
U2 - 10.1016/j.cclet.2024.110605
DO - 10.1016/j.cclet.2024.110605
M3 - 文章
AN - SCOPUS:105022691258
SN - 1001-8417
VL - 37
JO - Chinese Chemical Letters
JF - Chinese Chemical Letters
IS - 2
M1 - 110605
ER -