High-Energy-Density Hydrogen-Ion-Rocking-Chair Hybrid Supercapacitors Based on Ti3C2Tx MXene and Carbon Nanotubes Mediated by Redox Active Molecule

超级电容器 MXenes公司 材料科学 电容 阳极 阴极 电解质 碳纳米管 纳米技术 光电子学 电极 化学 物理化学
作者
Minmin Hu,Cong Cui,Chao Shi,Zhong‐Shuai Wu,Jinxing Yang,Renfei Cheng,Tianjia Guang,Qiang Cai,Hongxia Lu,Xiaohui Wang
出处
期刊:ACS Nano [American Chemical Society]
卷期号:13 (6): 6899-6905 被引量:136
标识
DOI:10.1021/acsnano.9b01762
摘要

MXenes have emerged as promising high-volumetric-capacitance supercapacitor electrode materials, whereas their voltage windows are not wide. This disadvantage prevents MXenes from being made into aqueous symmetric supercapacitors with high energy density. To attain high energy density, constructing asymmetric supercapacitors is a reliable design choice. Here, we propose a strategy to achieve high energy density of hydrogen ion aqueous-based hybrid supercapacitors by integrating a negative electrode of Ti3C2Tx MXene and a positive electrode of redox-active hydroquinone (HQ)/carbon nanotubes. The two electrodes are separated by a Nafion film that is proton permeable in H2SO4 electrolyte. Upon charging/discharging, hydrogen ions shuttle back and forth between the cathode and anode for charge compensation. The proton-induced high capacitance of MXene and HQ, along with complementary working voltage windows, simultaneously enhance the electrochemical performance of the device. Specifically, the hybrid supercapacitors operate in a 1.6 V voltage window and deliver a high energy density of 62 Wh kg–1, which substantially exceeds those of the state-of-the-art aqueous asymmetric supercapacitors reported so far. Additionally, the device exhibits excellent cycling stability and the all-solid-state planar hybrid supercapacitor displays exceptional flexibility and integration for bipolar cells to boost the capacitance and voltage output. These encouraging results provide the possibility of designing high-energy-density noble-metal-free asymmetric supercapacitors for practical applications.
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