TY - JOUR
T1 - Topological Insulator Heterojunction with Electric Dipole Domain to Boost Polysulfide Conversion in Lithium-Sulfur Batteries
AU - Chen, Hedong
AU - Qiu, Yecheng
AU - Cai, Zhiyuan
AU - Liang, Wenhao
AU - Liu, Lin
AU - Li, Manman
AU - Hou, Xianhua
AU - Chen, Fuming
AU - Zhou, Xunzhu
AU - Cheng, Tengfei
AU - He, Liqing
AU - Wang, Jiazhao
AU - Zhang, Xiao
AU - Dou, Shixue
AU - Li, Lin
N1 - Publisher Copyright:
© 2025 Wiley-VCH GmbH.
PY - 2025/3/24
Y1 - 2025/3/24
N2 - The heterojunction materials are considered as promising electrocatalyst candidates that empower advanced lithium-sulfur (Li−S) batteries. However, the detailed functional mechanism of heterojunction materials to boost the sulfur redox reaction kinetics remains unclear. Herein, we construct a multifunctional potential well-type Bi2Te3/TiO2 topological insulator (TI) heterojunction with electric dipole domain to elucidate the synergistic mechanism, which facilitates rapid mass transport, strengthens polysulfide capture ability and accelerates polysulfide conversion. Therefore, the Li−S battery with Bi2Te3/TiO2 TI heterojunction modified separator achieves high utilization of sulfur cathode, delivering a high reversible specific capacity of 1375 mAh g−1 at 0.2 C and long cycling capability with a negligible capacity decay of 0.022 % per cycle over 1000 cycles at 1 C. Even with the high sulfur loading of 13.2 mg cm−2 and low E/S ratio of 3.8 μL mg−1, a high area capacity of 11.2 mAh cm−2 and acceptable cycling stability can be obtained. This work provides guidance for designing high-efficiency TI heterojunctions to promote the practical application of Li−S batteries.
AB - The heterojunction materials are considered as promising electrocatalyst candidates that empower advanced lithium-sulfur (Li−S) batteries. However, the detailed functional mechanism of heterojunction materials to boost the sulfur redox reaction kinetics remains unclear. Herein, we construct a multifunctional potential well-type Bi2Te3/TiO2 topological insulator (TI) heterojunction with electric dipole domain to elucidate the synergistic mechanism, which facilitates rapid mass transport, strengthens polysulfide capture ability and accelerates polysulfide conversion. Therefore, the Li−S battery with Bi2Te3/TiO2 TI heterojunction modified separator achieves high utilization of sulfur cathode, delivering a high reversible specific capacity of 1375 mAh g−1 at 0.2 C and long cycling capability with a negligible capacity decay of 0.022 % per cycle over 1000 cycles at 1 C. Even with the high sulfur loading of 13.2 mg cm−2 and low E/S ratio of 3.8 μL mg−1, a high area capacity of 11.2 mAh cm−2 and acceptable cycling stability can be obtained. This work provides guidance for designing high-efficiency TI heterojunctions to promote the practical application of Li−S batteries.
KW - electric dipole domain
KW - functional mechanism
KW - Lithium-sulfur battery
KW - polysulfide conversion
KW - topological insulator heterojunction
UR - https://www.scopus.com/pages/publications/105001087185
U2 - 10.1002/anie.202423357
DO - 10.1002/anie.202423357
M3 - Journal article
C2 - 39743867
AN - SCOPUS:105001087185
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 13
M1 - e202423357
ER -