Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 355, P. 124189 - 124189
Published: May 11, 2024
Language: Английский
Applied Catalysis B Environment and Energy, Journal Year: 2024, Volume and Issue: 355, P. 124189 - 124189
Published: May 11, 2024
Language: Английский
Applied Catalysis B Environment and Energy, Journal Year: 2022, Volume and Issue: 315, P. 121523 - 121523
Published: May 18, 2022
Language: Английский
Citations
145Proceedings of the National Academy of Sciences, Journal Year: 2023, Volume and Issue: 120(29)
Published: July 10, 2023
Single-atom catalysts (SACs) are a promising area in environmental catalysis. We report on bimetallic Co–Mo SAC that shows excellent performance activating peroxymonosulfate (PMS) for sustainable degradation of organic pollutants with high ionization potential (IP > 8.5 eV). Density Functional Theory (DFT) calculations and experimental tests demonstrate the Mo sites – Co SACs play critical role conducting electrons from to sites, leading 19.4-fold increase rate phenol compared CoCl 2 PMS group. The exhibit catalytic even under extreme conditions show long-term activation 10-d experiments, efficiently degrading 600 mg/L phenol. Moreover, catalyst has negligible toxicity toward MDA-MB-231, Hela, MCF-7 cells, making it an environmentally friendly option water treatment. Our findings have important implications design efficient remediation other applications biology medicine.
Language: Английский
Citations
134Environmental Science & Technology, Journal Year: 2023, Volume and Issue: 57(7), P. 2907 - 2917
Published: Feb. 7, 2023
The heterogeneous electro-Fenton (hetero-e-Fenton)-coupled electrocatalytic oxygen reduction reaction (ORR) is regarded as a promising strategy for ·OH production by simultaneously driving two-electron ORR toward H2O2 and stepped activating the as-generated to ·OH. However, high-efficiency electrogeneration of remains challengeable, it difficult synchronously obtain efficient catalysis both steps above on one catalytic site. In this work, we propose dual-atomic-site catalyst (CoFe DAC) cooperatively catalyze electrogeneration, where atomically dispersed Co sites are assigned enhance O2 intermediates Fe responsible activation CoFe DAC delivers higher rate 2.4 mmol L-1 min-1 gcat-1 than single-site Co-NC (0.8 gcat-1) Fe-NC (1.0 gcat-1). Significantly, hetero-e-Fenton process demonstrated be more energy-efficient actual coking wastewater treatment with an energy consumption 19.0 kWh kg-1 COD-1 other electrochemical technologies that reported values 29.7∼68.0 kW h COD-1. This study shows attractive advantages efficiency sustainability which should have fresh inspiration development new-generation technology.
Language: Английский
Citations
108Coordination Chemistry Reviews, Journal Year: 2022, Volume and Issue: 475, P. 214874 - 214874
Published: Oct. 15, 2022
Language: Английский
Citations
97Chemical Engineering Journal, Journal Year: 2022, Volume and Issue: 452, P. 139446 - 139446
Published: Sept. 27, 2022
Language: Английский
Citations
74Angewandte Chemie International Edition, Journal Year: 2023, Volume and Issue: 62(22)
Published: March 9, 2023
Efficient molecular oxygen activation (MOA) is the key to environmentally friendly catalytic oxidation reactions. In last decade, single-atomic-site catalysts (SASCs) with nearly 100 % atomic utilization and unique electronic structure have been widely investigated for MOA. However, single active site makes effect unsatisfactory difficult deal complex Recently, dual-atomic-site (DASCs) provided a new idea effective of (O2 ) due more diverse sites synergetic interactions among adjacent atoms. this review, we systematically summarized recent research progress DASCs MOA in heterogeneous thermo- electrocatalysis. Finally, look forward challenges application prospects construction
Language: Английский
Citations
52ACS Catalysis, Journal Year: 2024, Volume and Issue: 14(4), P. 2134 - 2143
Published: Jan. 25, 2024
The waste of carbon sources and greenhouse gas production during wastewater treatment have become extremely important environmental issues. Herein, the BiOBr/BiVO4 compounds with defect-induced frustrated Lewis acid–base pairs (DFLPs) internal charge transfer were fabricated to convert organic pollutants into CO nearly 100% selectivity. oxygen vacancy (Ov) induced built-in electric field in create directional from BiOBr BiVO4. Density functional theory (DFT) calculations prove that Ov combines its adjacent hydroxyls form DFLP active sites can additionally capture activate CO2. Meanwhile, reduce formation-free energy COOH* intermediates, which is key rate-limiting step CO2 high This system has achieved selective conversion value-added chemicals pollutant degradation provides a theoretical basis for actual recycling sources.
Language: Английский
Citations
29Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 486, P. 150217 - 150217
Published: March 7, 2024
Language: Английский
Citations
21Journal of Hazardous Materials, Journal Year: 2024, Volume and Issue: 467, P. 133756 - 133756
Published: Feb. 13, 2024
Language: Английский
Citations
20Environmental Science & Technology, Journal Year: 2024, Volume and Issue: unknown
Published: Feb. 7, 2024
Catalyzed reduction processes have been recognized as important and supplementary technologies for water treatment, with the specific aims of resource recovery, enhancement bio/chemical-treatability persistent organic pollutants, safe handling oxygenate ions. Palladium (Pd) has widely used a catalyst/electrocatalyst in these processes. However, due to limited reserves high cost Pd, it is essential gain better understanding Pd-catalyzed decontamination process design affordable sustainable Pd catalysts. This review provides systematic summary recent advances reductive designing Pd-based nanocatalysts treatment water-borne special focus on interactions transformation mechanisms pollutant molecules catalysts at atomic scale. The discussion begins by examining adsorption pollutants onto sites from thermodynamic viewpoint. followed an explanation molecular-level reaction mechanism, demonstrating how electron-donors participate pollutants. Next, influence reactive site structure catalytic performance explored. Additionally, facilitating oxidation briefly discussed. longevity catalysts, crucial factor determining their practicality, also examined. Finally, we argue increased attention mechanism study, well precise construction under batch synthesis conditions, use catalysts/electrocatalysts concentrated facilitate recovery.
Language: Английский
Citations
18