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Innovative mechanical exfoliation process of screen-printed CNT-integrated Fe2NiSi-NiSi electrocatalyst for efficient water-splittingopen access

Authors
Abbas, Sayed ZafarVikraman, DhanasekaranSheikh, Zulfqar AliMehdi, Syed Muhammad ZainHussain, IftikharGoak, Jeung ChoonKim, Hyun-SeokJung, JongwanHussain, SajjadLee, Naesung
Issue Date
Feb-2026
Publisher
Elsevier Ltd
Keywords
CNT; HER; Mechanical exfoliation; OER; Screen-printing; Transition metal silicide; Vacuum annealing
Citation
Renewable Energy, v.258, pp 1 - 13
Pages
13
Indexed
SCIE
SCOPUS
Journal Title
Renewable Energy
Volume
258
Start Page
1
End Page
13
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/62584
DOI
10.1016/j.renene.2025.124927
ISSN
0960-1481
1879-0682
Abstract
Synthesis of cost-effective, high-performance electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) remains challenging. Herein, we report a novel approach to the synthesis of efficient electrocatalyst using silicon (Si), nickel (Ni), and carbon nanotube (CNT) on a Kovar (nickel-cobalt ferrous alloy) substrate via screen-printing and vacuum annealing. Initially, Si nanoparticles were screen-printed on a Kovar substrate. Subsequent vacuum annealing induces a solid-state diffusion reaction between Si and substrate, resulting in the formation of an Fe<inf>2</inf>NiSi Heusler phase that enriched catalytically active Fe and Ni metals. To further enhance catalytic activity, the unreacted Si was eliminated by introducing Ni nanoparticles, converting Si to an electrically conductive NiSi phase. Furthermore, these phases agglomerate at high temperatures, resulting in poor catalytic activities. The incorporation of CNT suppressed agglomeration, improved conductivity, and enhanced surface area. Additionally, the mechanical exfoliation strategy which is the key innovation of this study offers high exposure to active sites by protruding buried catalytic sites. The resulting CNT-Integrated Fe<inf>2</inf>NiSi-NiSi electrocatalyst demonstrated low overpotentials of 57 mV for HER and 200 mV for OER at 10 mA cm−2. As a bifunctional catalyst, it delivered an electrolyzer cell voltage of 1.491 V, comparable to conventional electrode systems. © 2025 Elsevier Ltd
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