Electron Beam Irradiation-Induced Defects Enhance Pt-TiO2 Photothermal Catalytic Degradation in PAEs: A Performance and Mechanism Study DOI Creative Commons
Fukun Bi,

Yaofei Zhang,

Zhuoxuan Zhou

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(3), P. 697 - 697

Published: Feb. 5, 2025

Phthalic acid esters (PAEs), ubiquitous semi-volatile organic compounds (SVOCs) in indoor environments, pose adverse effects on human health. However, their degradation mechanisms and pathways remain unclear. Herein, we developed an efficient photothermal catalyst by introducing defects (oxygen vacancies, OVs) TiO2 (P25) surfaces via electron beam irradiation technology with different doses (100, 300, 500, 700 kGy). The was employed as a support to prepare Pt-TiO2 catalysts for the of di (2-ethylhexyl) phthalate (DEMP) dimethyl (DMP), two representative PAEs. pre-treated 300 kGy dose supported Pt (Pt-Ti-P-300) presented optimal catalytic performance DEMP DMP degradation. Characterization results confirmed that OVs were successfully introduced catalysts. Meanwhile, induced expanded light absorption range improved generation separation photogenerated carriers, which significantly enhanced activity PAE Importantly, mechanism pathway further explored using situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) gas chromatography–mass spectrometry (GC-MS). These findings provide important insights into irradiation-mediated regulation removal PAEs environments.

Language: Английский

Durable Ru Nanocrystal with HfO2 Modification for Acidic Overall Water Splitting DOI Creative Commons
Xiangkai Kong, Jie Xu,

Zhicheng Ju

et al.

Nano-Micro Letters, Journal Year: 2024, Volume and Issue: 16(1)

Published: April 30, 2024

Durable and efficient bi-functional catalyst, that is capable of both oxygen evolution reaction hydrogen under acidic condition, are highly desired for the commercialization proton exchange membrane water electrolysis. Herein, we report a robust L-Ru/HfO

Language: Английский

Citations

18

Boosting hydrogen evolution reaction activity of Ru anchored binary oxyhydroxide by F-doping in alkaline seawater DOI
Jiawei Zhu,

Jing‐Qi Chi,

Xuanyi Wang

et al.

Nano Energy, Journal Year: 2024, Volume and Issue: 121, P. 109249 - 109249

Published: Jan. 3, 2024

Language: Английский

Citations

17

In situ construction of layered transition metal phosphides/sulfides heterostructures for efficient hydrogen evolution in acidic and alkaline media DOI

Yongteng Qian,

Yue Sun,

Fangfang Zhang

et al.

Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 490, P. 151693 - 151693

Published: April 26, 2024

Language: Английский

Citations

16

Synergistic Atomic Environment Optimization of Nickel–Iron Dual Sites by Co Doping and Cr Vacancy for Electrocatalytic Oxygen Evolution DOI

Hua‐Jie Niu,

Nian Ran,

Wei Zhou

et al.

Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 8, 2025

The dual-site synergistic catalytic mechanism on NiFeOOH suggests weak adsorption of Ni sites and strong Fe limited its activity toward alkaline oxygen evolution reaction (OER). Large-scale density functional theory (DFT) calculations confirm that Co doping can increase adsorption, while the metal vacancy reduce adsorption. combined two factors further modulate atomic environment optimize free energy oxygen-containing intermediates, thus enhancing OER activity. Accordingly, we used Cr vacancies to fabricate an amorphous catalyst VCr,Co-NiFeOOH. It provides overpotential 239 mV at 100 mA cm–2 high stability over 500 h with a ∼98% potential retention. resulting water electrolyzer based anion exchange membrane (AEM) exhibits remarkable performance 1 A 1.68 V in M KOH. XPS, soft-XAS, XANES Bader charge analysis results reveal regulation local microenvironment valence state by doping, improving sites. alleviate DFT effect redistribute Ni/Fe sites, d-band center Fe, endow Ni–Fe dual barrier rate-determining step.

Language: Английский

Citations

9

Electron Beam Irradiation-Induced Defects Enhance Pt-TiO2 Photothermal Catalytic Degradation in PAEs: A Performance and Mechanism Study DOI Creative Commons
Fukun Bi,

Yaofei Zhang,

Zhuoxuan Zhou

et al.

Molecules, Journal Year: 2025, Volume and Issue: 30(3), P. 697 - 697

Published: Feb. 5, 2025

Phthalic acid esters (PAEs), ubiquitous semi-volatile organic compounds (SVOCs) in indoor environments, pose adverse effects on human health. However, their degradation mechanisms and pathways remain unclear. Herein, we developed an efficient photothermal catalyst by introducing defects (oxygen vacancies, OVs) TiO2 (P25) surfaces via electron beam irradiation technology with different doses (100, 300, 500, 700 kGy). The was employed as a support to prepare Pt-TiO2 catalysts for the of di (2-ethylhexyl) phthalate (DEMP) dimethyl (DMP), two representative PAEs. pre-treated 300 kGy dose supported Pt (Pt-Ti-P-300) presented optimal catalytic performance DEMP DMP degradation. Characterization results confirmed that OVs were successfully introduced catalysts. Meanwhile, induced expanded light absorption range improved generation separation photogenerated carriers, which significantly enhanced activity PAE Importantly, mechanism pathway further explored using situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) gas chromatography–mass spectrometry (GC-MS). These findings provide important insights into irradiation-mediated regulation removal PAEs environments.

Language: Английский

Citations

2