Xuyao Qiao , Shuguang Ning , Hongyao Zhao , Ruiting Ni , Wanyu Zhang , Yangping Zhang , Linzhi Zhai , Danhong Shang , Yanyun Wang , Tongyi Yang , Mengnan Wang , Fu Yang
{"title":"将光fenton -like Fe3O4/CdS-O模块集成到海绵基凝胶太阳能蒸发器中,协同水再生和污染物降解","authors":"Xuyao Qiao , Shuguang Ning , Hongyao Zhao , Ruiting Ni , Wanyu Zhang , Yangping Zhang , Linzhi Zhai , Danhong Shang , Yanyun Wang , Tongyi Yang , Mengnan Wang , Fu Yang","doi":"10.1016/j.jece.2025.117247","DOIUrl":null,"url":null,"abstract":"<div><div>Addressing the dual challenges of freshwater scarcity and pollution elimination requires innovative technologies that rationally integrate multiple functions. This study developed a representative dual-functional solar evaporator by coupling photothermal Fe₃O₄ nanospheres with oxygen-doped CdS (CdS-O) within a sponge-based hydrogel matrix, achieving concurrent high-efficiency solar-driven water regeneration and pollutant degradation. The design leverages the unique roles of two unique components, wherein, Fe₃O₄ endows the evaporator with broadband solar absorption (300–800 nm) and an superior photothermal conversion efficiency of 80 %, while oxygen doping CdS-O narrows its bandgap (from 2.31 eV to 2.29 eV), enhancing visible-light harvesting and charge separation. Crucially, the synergistic interplay between Fe₃O₄ and CdS-O establishes a self-sustained photo-Fenton-like mechanism. CdS-O generates H₂O₂ via photogenerated electron reduction of O₂, and Fe₃O₄ acts as an electron acceptor to accelerate Fe<sup>3 +</sup>/Fe<sup>2+</sup> cycling, Fe²⁺ ions react with H₂O₂ via a Fenton-like process to produce ·OH radicals for pollutant mineralization. Simultaneously, the hydrogel-sponge architecture ensures rapid water transport and localized heat confinement, enabling an evaporation rate of 1.55 kg·m<sup>−2</sup>·h<sup>−1</sup> under 1 sun irradiation. The system demonstrates remarkable dual-functionality: 86.9 % tetracycline degradation in lake water within 240 minutes and 89 % photocatalytic activity retention after six cycles. This work overcomes the limitations of conventional single-function systems by unifying photothermal evaporation and photocatalytic oxidation into a scalable platform, offering a sustainable solution for simultaneous water production and purification through material synergy and energy-efficient design.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":"13 4","pages":"Article 117247"},"PeriodicalIF":7.4000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Integrating photo-Fenton-like Fe3O4/CdS-O modules into sponge-based gel solar evaporator for synergistic water regeneration and pollutant degradation\",\"authors\":\"Xuyao Qiao , Shuguang Ning , Hongyao Zhao , Ruiting Ni , Wanyu Zhang , Yangping Zhang , Linzhi Zhai , Danhong Shang , Yanyun Wang , Tongyi Yang , Mengnan Wang , Fu Yang\",\"doi\":\"10.1016/j.jece.2025.117247\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Addressing the dual challenges of freshwater scarcity and pollution elimination requires innovative technologies that rationally integrate multiple functions. This study developed a representative dual-functional solar evaporator by coupling photothermal Fe₃O₄ nanospheres with oxygen-doped CdS (CdS-O) within a sponge-based hydrogel matrix, achieving concurrent high-efficiency solar-driven water regeneration and pollutant degradation. The design leverages the unique roles of two unique components, wherein, Fe₃O₄ endows the evaporator with broadband solar absorption (300–800 nm) and an superior photothermal conversion efficiency of 80 %, while oxygen doping CdS-O narrows its bandgap (from 2.31 eV to 2.29 eV), enhancing visible-light harvesting and charge separation. Crucially, the synergistic interplay between Fe₃O₄ and CdS-O establishes a self-sustained photo-Fenton-like mechanism. CdS-O generates H₂O₂ via photogenerated electron reduction of O₂, and Fe₃O₄ acts as an electron acceptor to accelerate Fe<sup>3 +</sup>/Fe<sup>2+</sup> cycling, Fe²⁺ ions react with H₂O₂ via a Fenton-like process to produce ·OH radicals for pollutant mineralization. Simultaneously, the hydrogel-sponge architecture ensures rapid water transport and localized heat confinement, enabling an evaporation rate of 1.55 kg·m<sup>−2</sup>·h<sup>−1</sup> under 1 sun irradiation. The system demonstrates remarkable dual-functionality: 86.9 % tetracycline degradation in lake water within 240 minutes and 89 % photocatalytic activity retention after six cycles. 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Integrating photo-Fenton-like Fe3O4/CdS-O modules into sponge-based gel solar evaporator for synergistic water regeneration and pollutant degradation
Addressing the dual challenges of freshwater scarcity and pollution elimination requires innovative technologies that rationally integrate multiple functions. This study developed a representative dual-functional solar evaporator by coupling photothermal Fe₃O₄ nanospheres with oxygen-doped CdS (CdS-O) within a sponge-based hydrogel matrix, achieving concurrent high-efficiency solar-driven water regeneration and pollutant degradation. The design leverages the unique roles of two unique components, wherein, Fe₃O₄ endows the evaporator with broadband solar absorption (300–800 nm) and an superior photothermal conversion efficiency of 80 %, while oxygen doping CdS-O narrows its bandgap (from 2.31 eV to 2.29 eV), enhancing visible-light harvesting and charge separation. Crucially, the synergistic interplay between Fe₃O₄ and CdS-O establishes a self-sustained photo-Fenton-like mechanism. CdS-O generates H₂O₂ via photogenerated electron reduction of O₂, and Fe₃O₄ acts as an electron acceptor to accelerate Fe3 +/Fe2+ cycling, Fe²⁺ ions react with H₂O₂ via a Fenton-like process to produce ·OH radicals for pollutant mineralization. Simultaneously, the hydrogel-sponge architecture ensures rapid water transport and localized heat confinement, enabling an evaporation rate of 1.55 kg·m−2·h−1 under 1 sun irradiation. The system demonstrates remarkable dual-functionality: 86.9 % tetracycline degradation in lake water within 240 minutes and 89 % photocatalytic activity retention after six cycles. This work overcomes the limitations of conventional single-function systems by unifying photothermal evaporation and photocatalytic oxidation into a scalable platform, offering a sustainable solution for simultaneous water production and purification through material synergy and energy-efficient design.
期刊介绍:
The Journal of Environmental Chemical Engineering (JECE) serves as a platform for the dissemination of original and innovative research focusing on the advancement of environmentally-friendly, sustainable technologies. JECE emphasizes the transition towards a carbon-neutral circular economy and a self-sufficient bio-based economy. Topics covered include soil, water, wastewater, and air decontamination; pollution monitoring, prevention, and control; advanced analytics, sensors, impact and risk assessment methodologies in environmental chemical engineering; resource recovery (water, nutrients, materials, energy); industrial ecology; valorization of waste streams; waste management (including e-waste); climate-water-energy-food nexus; novel materials for environmental, chemical, and energy applications; sustainability and environmental safety; water digitalization, water data science, and machine learning; process integration and intensification; recent developments in green chemistry for synthesis, catalysis, and energy; and original research on contaminants of emerging concern, persistent chemicals, and priority substances, including microplastics, nanoplastics, nanomaterials, micropollutants, antimicrobial resistance genes, and emerging pathogens (viruses, bacteria, parasites) of environmental significance.