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Visible-light-driven hydrogen generation from sanitation water using a bubble-like As2O3/Poly(2-chlorobenzeneamine) nanocomposite photocathode

delete2026-07-31
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PRE
AI
A
Amira Ben Gouider Trabelsi
F
Fatemah H. Alkallas
K
K. S. Almugren
A
Asmaa M. Elsayed *
M
Mohamed Rabia *
DOI:10.1007/s00289-026-06619-8delete
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Abstract

Abstract

En 中文
A novel arsenic(III) oxide/poly(2-chlorobenzeneamine) (As2O3/P2CBA) nanocomposite was synthesized via a one-pot chemical oxidative polymerization route using sodium arsenite (NaAsO2) and ammonium persulfate ((NH4)2S2O8) as oxidants. The resulting nanocomposite exhibited a distinctive bubble-like surface morphology and strong broadband optical absorption, accompanied by a narrow optical bandgap of 1.75 eV—underscoring its suitability for visible-light-driven photoelectrochemical applications. When employed as a photocathode, the As₂O₃/P2CBA nanocomposite achieved a current density in light (Jₚₕ) of − 0.018 mA cm⁻² under simulated solar irradiation. The hydrogen generation activity was further evaluated under incident photons with energies ranging from 1.7 to 3.6 eV, revealing pronounced photoresponsivity and energy-dependent current modulation. Remarkably, the hydrogen evolution reaction proceeded efficiently in tertiary-treated sanitation water without any additional supporting electrolyte, highlighting the material’s robustness in real-world water matrices. The synergistic combination of strong visible-light absorption, effective charge carrier separation, and electrolyte adaptability positions the As2O3/P2CBA nanocomposite as a promising platform for sustainable and scalable green hydrogen production. Its ability to harness non-conventional water sources further enhances its potential for deployment in decentralized and environmentally conscious energy systems.
Keywords:
As(III) oxide
Poly-2-chlorobenzeneamine
Hydrogen generation
Photocathode
Renewable energy

Journal

Polymer Bulletin cover
Polymer Bulletin
IF:
4
Papers:
8.5K
Citations:
1.5W

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college of science
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Faculty of Science
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