Enhanced electronic structure and electrochemical active area of ternary NiCoFe-LDH and Cu nanowire composites for superior energy storage

Authors
Eom, SubinJung, Moo YoungPark, JihyeSon, Ji-WonAhn, JeongHyeonKim, Sung WonYun, Yong JuJun, Yongseok
Issue Date
2026-01
Publisher
Elsevier BV
Citation
Journal of Energy Storage, v.144
Abstract
Climate change urgently necessitates the development of sustainable energy solutions alongside efficient energy storage devices. Among these, supercapacitors have emerged as promising candidates due to their fast charge/discharge capabilities and exceptional long-term cycle stability. In this study, NiCoFe-layered double hydroxide (NiCoFe-LDH) was successfully synthesized via electrodeposition onto copper nanowires (Cu NWs), which were prepared through electrochemical anodization followed by thermal reduction. The optimal Fe ratio in NiCoFe-LDH@Cu NW was determined through various electrochemical tests, with the 3-NiCoFe-LDH@Cu NW (Ni:Co:Fe = 5:3:3) exhibiting superior electrochemical performance, achieving a capacity of 130.20 μAh cm−2 at a current density of 3.0 mA cm−2. To evaluate practical applicability, an asymmetric supercapacitor (ASC) was fabricated using 3-NiCoFe-LDH@Cu NW as the positive electrode and 1-MXene@CuO NW as the negative electrode. The ASC demonstrated excellent energy storage performance, delivering an energy density of 1.69 mWh cm−2 at a power density of 19.27 mW cm−2, outperforming recently reported devices. Furthermore, the ASC retained 80.7 % of its initial capacity after 8000 cycles at 10 mA cm−2, with a coulombic efficiency of 102.9 %, highlighting its remarkable stability and efficiency.
Keywords
LAYERED DOUBLE HYDROXIDES; OXYGEN EVOLUTION; CHARGE STORAGE; PERFORMANCE; NI; CO; SUPERCAPACITORS; CARBON; Asymmetric supercapacitor; NiCoFe-LDH; Cu nanowire; MXene; Pseudocapacitor
ISSN
2352-152X
URI
https://pubs.kist.re.kr/handle/201004/154078
DOI
10.1016/j.est.2025.119690
Appears in Collections:
KIST Article > 2026
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

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

BROWSE