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Cu4SnS4-Functionalized Absorbent Pads-Derived Carbon as a Bifunctional Electrode for Supercapacitors and Hydrogen Evolution Reaction

delete2026-06-19
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OA
AI
R
Romiyo Justinabraham
A
Arulappan Durairaj
J
John H. T. Luong
S
Samuel Vasanthkumar *
M
Moorthy Maruthapandi *
DOI:10.3390/nano16120773delete
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Abstract

Abstract

En 中文
The conversion of bio-waste into functional energy materials provides a robust platform for addressing both environmental and energy challenges. In this paper, discarded absorbent pads are transformed into carbon-rich frameworks, which is followed by the fabrication of composites through the incorporation of Cu4SnS4 (CSS) for dual electrochemical applications. Integrating CSS into the waste-derived carbon matrix induces strong synergistic effects, improving electrical conductivity, increasing active-site availability, and accelerating charge-transfer kinetics. Comprehensive physicochemical analyses confirmed the successful formation of a well-integrated heterostructure composite with favorable structural and surface characteristics. Electrochemical evaluations further demonstrated that CSS-modified carbon exhibits superior bifunctional performance. In a two-electrode configuration, the composite delivers an energy density of 12.08 Wh kg−1 at a power density of 250 W kg−1 along with excellent cycling stability in supercapacitor applications. As an electrocatalyst, it achieves a low overpotential of 268 mV at −10 mA cm−2 and a small Tafel slope of 75 mV dec−1, reflecting efficient reaction kinetics. The strong durability observed in both systems underscores the structural integrity and long-term operational stability of the material. Overall, this paper advances a sustainable waste-to-resource strategy for fabricating multifunctional carbon-based composites, offering a promising platform for integrated energy-storage and hydrogen-generation technologies.
Keywords:
diaper waste
Cu<sub>4</sub>SnS<sub>4</sub>
energy storage
hydrogen evolution reaction

Journal

N
Nanomaterials
IF:
4.3
Papers:
2.2W
Citations:
8.1W

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Ariel University
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