A synergistic Ti3C2Tx/PPy bilayer electrochemical actuator

被引:11
|
作者
Pang, Di [1 ]
Wang, Xiaotong [1 ]
Liu, Chuanfang [1 ]
Xu, Huajun [1 ]
Chen, Gang [1 ,2 ]
Du, Fei [1 ,2 ]
Dall' Agnese, Yohan [3 ]
Gao, Yu [1 ]
机构
[1] Jilin Univ, Coll Phys, Key Lab Phys & Technol Adv Batteries Minist Educ, Changchun 130012, Peoples R China
[2] Jilin Univ, Coll Phys, State Key Lab Superhard Mat, Changchun 130012, PR, Peoples R China
[3] UCL, Inst Mat Discovery, London WC1E 7JE, England
关键词
Electrochemical actuators; MXene; PPy; Ti(3)C2T(x)/PPy bilayer film; GRAPHENE; MXENE;
D O I
10.1016/j.apsusc.2021.152403
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Electrochemical actuators are devices that directly convert electrical energy into mechanical energy and have a wide range of applications. MXenes have high energy density, excellent rate performance, high electronic conductivity, strong mechanical strength, and can store ions through fast intercalation mechanism, making it a promising material for actuator applications. However, the restacking of MXenes layers limits ion percolation and thus limits the actuation performance. Polypyrrole (PPy) has a large volume deformation during its redox reaction process, but its low electrical conductivity and weak mechanical strength limit its practical application. Here, we logically designed an electrochemical actuator with Ti3C2Tx/PPy bilayer film as the electrode, and the Ti3C2Tx layer effectively improved the electrical conductivity of Ti3C2Tx/PPy and acted as the same time as current collector, co-actuation, and conductive additive, effectively accelerating the redox reaction rate of the PPy layer and increasing the performance. The curvature change of Ti3C2Tx/PPy bilayer film was improved by 57% (at 5 mV/s) in aqueous 1 M LiClO4 compared to the pure PPy film. After 10,000 cycles, 69.2% of the initial actuation performance can still be maintained. This research proves that this electrode structure design is feasible to improve the performance of actuators.
引用
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页数:6
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