Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/121686
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: A 2.0 V capacitive device derived from shape-preserved metal nitride nanorods
Author: Zhu, C.
Sun, Y.
Chao, D.
Wang, X.
Yang, P.
Zhang, X.
Huang, H.
Zhang, H.
Fan, H.J.
Citation: Nano Energy, 2016; 26:1-6
Publisher: Elsevier
Issue Date: 2016
ISSN: 2211-2855
2211-3282
Statement of
Responsibility: 
Changrong Zhu, Yanfeng Sun, Dongliang Chao, Xinghui Wang, Peihua Yang, Xiao Zhang, Hui Huang, Hua Zhang, Hong Jin Fan
Abstract: A high working voltage and fast charging/discharging capability are important to a supercapacitor device in order to achieve decent energy densities with high power. In this work, we report 2.0 V quasi-solid-state symmetric capacitive device based on Fe2N-Ti2N (FTN) core-shell nanorod array electrodes. Through a surface protection by a thin and ultra-stable Ti2N shell, Fe2N converted from its oxyhydroxide precursor inhibits the original nanorod structure. Due to advantageous features of these core-shell metal nitride electrodes (e.g., high conductivity, structure stability, direct current path), the symmetric device permits ultrahigh scan rates (up to 50 V s−1) and delivers fairly stable capacitance in long-term cycles (~82 F g−1 with ~99% capacitance retention in 20,000 cycles). As a result, the supercapacitor exhibits an impressive energy density of ~48.5 W h kg−1 at the power of 2700 W kg−1. These results demonstrate the potentialities of metal nitride nanorods array for high energy density capacitive device.
Keywords: Symmetric supercapacitor; high working voltage; metal nitride; electrochemical capacitor; atomic layer deposition
Rights: © 2016 Elsevier Ltd. All rights reserved.
DOI: 10.1016/j.nanoen.2016.04.056
Published version: http://dx.doi.org/10.1016/j.nanoen.2016.04.056
Appears in Collections:Aurora harvest 8
Chemical Engineering publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.