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1.
Angew Chem Int Ed Engl ; : e202409179, 2024 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-39004946

RESUMO

Crystalline red phosphorus(CRP), known for its promising photocatalytic properties, faces challenges in photocatalytic hydrogen evolution(PHE) due to undesired inherent charge deep trapping and recombination effects induced by defects. This study overcomes these limitations through an innovative strategy in integrating ruthenium single atoms(Ru1) within CRP to simultaneously repair the intrinsic undesired vacancy defects and serve as the uniformly distributed anchoring sites for a controllable growth into ruthenium nanoparticles(RuNP). Hence, a highly functionalized CRP with Ru1 and RuNP(Ru1-NP/CRP) with concerted effects in regulating electronic structures and promoting interfacial charge transfer has been achieved. Advanced characterizations unveil the pioneering dual role of pre-anchored Ru1 in transforming CRP photocatalysis. The regulations of vacancy defects on the surface of CRP minimize the detrimental deep charge trapping, resulting in the prolonged lifetime of charges. With the well-distributed in-situ growth of RuNP on Ru1 sites, the constructed robust "bridge" that connects CRP and RuNP facilitates constructive interfacial charge transfer. Ultimately, the synergistic effect induced by the pre-anchored Ru1 endows Ru1-NP/CRP with an exceptional PHE rate of 3175µmolh-1g-1, positioning it as one of the most efficient elemental-based photocatalysts. This breakthrough underscores the crucial role of pre-anchoring metal single atoms at defect sites of catalysts in enhancing hydrogen production.

2.
ACS Nano ; 18(27): 17939-17949, 2024 Jul 09.
Artigo em Inglês | MEDLINE | ID: mdl-38918079

RESUMO

How to simultaneously utilize photogenerated electrons and holes still remains a critical challenge in the field of artificial photosynthesis, especially in the process of photocatalytic hydrogen (H2) evolution coupled with biomass oxidation to value-added chemicals. Herein, a series-parallel photocatalyst (Cu NPs/CdS/In2O3) that can intrinsically regulate the transfer of photogenerated carriers is ingeniously designed for photocatalytic H2 evolution synergized with furfural alcohol (FFA) selective oxidation to furfural (FF). Accordingly, the desired H2 and FF evolution rates with near 100% selectivity toward FF are achieved on Cu NPs/CdS/In2O3 in a sealed atmospheric system. Experimental and theoretical analyses confirm that the localized surface plasmon resonance (LSPR) effect induced by Cu NPs accelerates the reduction of protons (H+) to H2 efficiently, while the photogenerated holes from In2O3 preferentially activate the α-C-H bond of FFA adsorbed on Lewis acid sites to generate FF. This work provides a reference for regulating the transfer of photogenerated carriers for H2 evolution coupled with FF synthesis.

3.
Nanomaterials (Basel) ; 14(11)2024 May 24.
Artigo em Inglês | MEDLINE | ID: mdl-38869548

RESUMO

Creating oxygen vacancy in tungsten trioxide (WO3) has been considered as an effective strategy to improve the photocatalytic performance for degrading organic pollutants. In this study, oxygen vacancies were introduced into WO3 by thermal treatment under Ar atmosphere and their proportion was changed by setting different treatment times. WO3-x samples show better photoelectric properties and photocatalytic degradation performance for carbamazepine (CBZ) than an oxygen-vacancy-free sample, and WO3-x with the optimal proportion of oxygen vacancies is obtained by thermal treatment for 3 h in 550 °C. Furthermore, it discovers that the surface oxygen vacancies on WO3-x would be recovered when it is exposed to air, resulting in a bulk oxygen vacancy dominating WO3-x (bulk-WO3-x). The bulk-WO3-x exhibited much higher degradation efficiency for CBZ than WO3-x with both surface and bulk oxygen vacancies. The mechanism study shows bulk-WO3-x mainly degrades the CBZ by producing OH radicals and superoxide radicals, while oxygen-vacancy-free sample mainly oxidizes the CBZ by the photoexcited hole, which requires the CBZ to be adsorbed on the surface for degradation. The radical generated by bulk-WO3-x exhibits stronger oxidizing capacity by migrating to the solution for CBZ degradation. In summary, the influence of oxygen vacancy on photocatalytic degradation performance depends on both the proportion and location distribution and could lie in the optimization of the photodegradation mechanism. The results of this study could potentially broaden our understanding of the role of oxygen vacancies and provide optimal directions and methods for oxygen vacancy regulation for photocatalysts.

4.
Angew Chem Int Ed Engl ; 63(33): e202407090, 2024 Aug 12.
Artigo em Inglês | MEDLINE | ID: mdl-38840270

RESUMO

Low *CO coverage on the active sites is a major hurdle in the tandem electrocatalysis, resulting in unsatisfied C2H4 production efficiencies. In this work, we developed a synergetic-tandem strategy to construct a copper-based composite catalyst for the electroreduction of CO2 to C2H4, which was constructed via the template-directed polymerization of ultrathin Cu(II) porphyrin organic framework incorporating atomically isolated Cu(II) porphyrin and Cu(II) bipyridine sites on a carbon nanotube (CNT) scaffold, and then Cu2O nanoparticles were uniformly dispersed on the CNT scaffold. The presence of dual active sites within the Cu(II) porphyrin organic framework create a synergetic effect, leading to an increase in local *CO availability to enhance the C-C coupling step implemented on the adjacent Cu2O nanoparticles for further C2H4 production. Accordingly, the resultant catalyst affords an exceptional CO2-to-C2H4 Faradaic efficiency (FEC2H4) of 71.0 % at -1.1 V vs reversible hydrogen electrode (RHE), making it one of the most effective copper-based tandem catalysts reported to date. The superior performance of the catalyst is further confirmed through operando infrared spectroscopy and theoretic calculations.

5.
Environ Sci Technol ; 58(9): 4404-4414, 2024 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-38310571

RESUMO

Photocatalytic oxidation has gained great interest in environmental remediation, but it is still limited by its low efficiency and catalytic deactivation in the degradation of aromatic VOCs. In this study, we concurrently regulated the surface hydroxyl and oxygen vacancies by introducing Al into ZnSn layered double hydroxide (LDH). The presence of distorted Al species induced local charge redistribution, leading to the remarkable formation of oxygen vacancies. These oxygen vacancies subsequently increased the amount of surface hydroxyl and elongated its bond length. The synergistic effects of surface hydroxyl and oxygen vacancies greatly enhanced reactant adsorption-activation and facilitated charge transfer to generate •OH, •O2-, and 1O2, resulting in highly efficient oxidation and ring-opening of various aromatic VOCs. Compared with commercial TiO2, the optimized ZnSnAl-50 catalyst exhibited about 2-fold activity for the toluene and styrene degradation and 10-fold activity for the chlorobenzene degradation. Moreover, ZnSnAl-50 demonstrated exceptional stability in the photocatalytic oxidation of toluene under a wide humidity range of 0-75%. This work marvelously improves the photocatalytic efficiency, stability, and adaptability through a novel strategy of surface hydroxyl and oxygen vacancies engineering.


Assuntos
Radical Hidroxila , Oxigênio , Adsorção , Oxirredução , Tolueno
6.
J Hazard Mater ; 466: 133611, 2024 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-38290338

RESUMO

Singlet oxygen (1O2) is a highly effective reactive species in selectively oxidizing organic pollutants. However, it is still challenging to rationally design robust catalysts for the selective generation of 1O2. Herein, the coordination and engineering architecture of the foam board-like CoSe2 alloy were facilely constructed through a green solvent-free method and displayed almost 100% 1O2 production selectivity. The CoSe2 alloy showed excellent catalytic ability for the efficient and fast removal of organic pollutants via peroxymonosulfate (PMS) activation compared with previously reported cobalt-based catalysts. The CoSe2/PMS system exhibited strong resistance for a broad pH range (3.0-11.0) and various coexisting inorganic ions owing to the advantage of the strong bonding of Co-Se in CoSe2 alloy. Mechanism studies revealed that 1O2 was the only reactive oxygen species in the CoSe2/PMS system. Theoretical calculations demonstrated that Co was the dominant adsorption site for PMS in CoSe2, and the production pathway of 1O2 was PMS* â†’ *OH → *O → 1O2. In addition, it was proved that *OH and *O served as the rate-determining steps for the formation of 1O2 by PMS activation on CoSe2 alloy. These findings provide a rational strategy for preparing a series of low-cost transition metal-based alloy catalysts for PMS activation to achieve high-efficiency 1O2 production in the elimination of organic pollutants.

7.
Nanomicro Lett ; 16(1): 5, 2023 Nov 06.
Artigo em Inglês | MEDLINE | ID: mdl-37930462

RESUMO

We report a novel double-shelled nanoboxes photocatalyst architecture with tailored interfaces that accelerate quantum efficiency for photocatalytic CO2 reduction reaction (CO2RR) via Mo-S bridging bonds sites in Sv-In2S3@2H-MoTe2. The X-ray absorption near-edge structure shows that the formation of Sv-In2S3@2H-MoTe2 adjusts the coordination environment via interface engineering and forms Mo-S polarized sites at the interface. The interfacial dynamics and catalytic behavior are clearly revealed by ultrafast femtosecond transient absorption, time-resolved, and in situ diffuse reflectance-Infrared Fourier transform spectroscopy. A tunable electronic structure through steric interaction of Mo-S bridging bonds induces a 1.7-fold enhancement in Sv-In2S3@2H-MoTe2(5) photogenerated carrier concentration relative to pristine Sv-In2S3. Benefiting from lower carrier transport activation energy, an internal quantum efficiency of 94.01% at 380 nm was used for photocatalytic CO2RR. This study proposes a new strategy to design photocatalyst through bridging sites to adjust the selectivity of photocatalytic CO2RR.

8.
J Hazard Mater ; 457: 131781, 2023 09 05.
Artigo em Inglês | MEDLINE | ID: mdl-37315412

RESUMO

Black-odorous urban rivers can serve as reservoirs for heavy metals and other pollutants, in which sewage-derived labile organic matter triggering the water blackening and odorization largely determine the fate and ecological impact of the heavy metals. Nonetheless, information on the pollution and ecological risk of heavy metals and their reciprocal impact on microbiome in organic matter-polluted urban rivers remain unknown. In this study, sediment samples were collected and analyzed from 173 typical black-odorous urban rivers in 74 cities across China, providing a comprehensive nationwide assessment of heavy metal contamination. The results revealed substantial contamination levels of 6 heavy metals (i.e., Cu, Zn, Pb, Cr, Cd, and Li), with average concentrations ranging from 1.85 to 6.90 times higher than their respective background values in soil. Notably, the southern, eastern, and central regions of China exhibited particularly elevated contamination levels. In comparison to oligotrophic and eutrophic waters, the black-odorous urban rivers triggered by organic matter exhibited significantly higher proportions of the unstable form of these heavy metals, indicating elevated ecological risks. Further analyses suggested the critical roles of organic matter in shaping the form and bioavailability of heavy metals through fueling microbial processes. In addition, most heavy metals had significantly higher but varied impact on the prokaryotic populations relative to eukaryotes.


Assuntos
Metais Pesados , Poluentes Químicos da Água , Monitoramento Ambiental/métodos , Rios , Medição de Risco , Metais Pesados/análise , China , Poluentes Químicos da Água/análise , Sedimentos Geológicos
9.
JACS Au ; 3(4): 1230-1240, 2023 Apr 24.
Artigo em Inglês | MEDLINE | ID: mdl-37124295

RESUMO

Engineering the interfacial structure between noble metals and oxides, particularly on the surface of non-reducible oxides, is a challenging yet promising approach to enhancing the performance of heterogeneous catalysts. The interface site can alter the electronic and d-band structure of the metal sites, facilitating the transition of energy levels between the reacting molecules and promoting the reaction to proceed in a favorable direction. Herein, we created an active Pd-Si interface with tunable electronic metal-support interaction (EMSI) by growing a thin permeable silica layer on a non-reducible oxide ZSM-5 surface (termed Pd@SiO2/ZSM-5). Our experimental results, combined with density functional theory calculations, revealed that the Pd-Si active interface enhanced the charge transfer from deposited Si to Pd, generating an electron-enriched Pd surface, which significantly lowered the activation barriers for O2 and H2O. The resulting reactive oxygen species, including O2 -, O2 2-, and -OH, synergistically facilitated formaldehyde oxidation. Additionally, moderate electronic metal-support interaction can promote the catalytic cycle of Pd0 ⇆ Pd2+, which is favorable for the adsorption and activation of reactants. This study provides a promising strategy for the design of high-performance noble metal catalysts for practical applications.

10.
Nat Commun ; 14(1): 1890, 2023 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-37019917

RESUMO

Electrochemical water oxidation enables the conversion of H2O to H2O2. It holds distinct advantages to the O2 reduction reaction, which is restricted by the inefficient mass transfer and limited solubility of O2 in aqueous media. Nonetheless, most reported anodes suffer from high overpotentials (usually >1000 mV) and low selectivity. Electrolysis at high overpotentials often causes serious decomposition of peroxides and leads to declined selectivity. Herein, we report a ZnGa2O4 anode with dual active sites to improve the selectivity and resist the decomposition of peroxides. Its faradaic efficiency reaches 82% at 2.3 V versus RHE for H2O2 generation through both direct (via OH-) and indirect (via HCO3-) pathways. The percarbonate is the critical species generated through the conversion of bicarbonate at Ga-Ga dual sites. The peroxy bond is stable on the surface of the ZnGa2O4 anode, significantly improving faradaic efficiency.

11.
Environ Sci Technol ; 57(12): 5024-5033, 2023 03 28.
Artigo em Inglês | MEDLINE | ID: mdl-36892275

RESUMO

Efficient spontaneous molecular oxygen (O2) activation is an important technology in advanced oxidation processes. Its activation under ambient conditions without using solar energy or electricity is a very interesting topic. Low valence copper (LVC) exhibits theoretical ultrahigh activity toward O2. However, LVC is difficult to prepare and suffers from poor stability. Here, we first report a novel method for the fabrication of LVC material (P-Cu) via the spontaneous reaction of red phosphorus (P) and Cu2+. Red P, a material with excellent electron donating ability and can directly reduce Cu2+ in solution to LVC via forming Cu-P bonds. With the aid of the Cu-P bond, LVC maintains an electron-rich state and can rapidly activate O2 to produce ·OH. By using air, the ·OH yield reaches a high value of 423 µmol g-1 h-1, which is higher than traditional photocatalytic and Fenton-like systems. Moreover, the property of P-Cu is superior to that of classical nano-zero-valent copper. This work first reports the concept of spontaneous formation of LVC and develops a novel avenue for efficient O2 activation under ambient conditions.


Assuntos
Cobre , Peróxido de Hidrogênio , Peróxido de Hidrogênio/química , Fósforo , Oxirredução , Oxigênio
12.
Small ; 19(24): e2300114, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-36919559

RESUMO

In situ generation of hydrogen peroxide (H2 O2 ) has attracted extensive attention, especially in water treatment. However, traditional anthraquinones can only produce high-concentration H2 O2 and its transportation and storage are not convenient and dangerous. Herein, an in situ and on-demand strategy to produce H2 O2 by using a cascade water electrolysis together with a heterocatalysis system is provided. Beginning with water, H2, and O2 can be generated via electrolysis and then react with each other to produce H2 O2 immediately on efficient zeolite-encaged ultrasmall Pd catalysts. Significantly, the H2 O2 generation rate in the optimized cascade system reaches up to 0.85 mol L-1 h-1 gPd -1 , overcoming most of the state-of-the-art catalysts in previous literature. The confinement effect of zeolites is not only beneficial to the formation of highly dispersed metal species, promoting the H2 O2 generation, but also inhibits the H2 O2 decomposition, enhancing the production yield of H2 O2 . In addition, the effect of electrolytes, sizes of Pd species, as well as zeolite acidity are also systematically studied. This work provides a new avenue for H2 O2 generation via a highly efficient cascade electrolysis-heterocatalysis system by using zeolite-supported metal catalysts. The high catalytic efficiency and green process for H2 O2 generation make it very promising for further practical applications.

13.
J Hazard Mater ; 452: 131210, 2023 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-36958162

RESUMO

Singlet oxygen (1O2), which is difficult to generate, plays an important role in chemosynthesis, biomedicine and environment. Molecular oxygen (O2) is a green oxidant to produce 1O2 cost-effectively. However, O2 activation is difficult due to its spin-forbidden nature. Moreover, the main products of O2 activation are basically hydrogen peroxide (H2O2) and hydroxyl radical (•OH), but rarely 1O2. Herein, we innovatively realize the selective generation of 1O2 via O2 activation by a facile molybdenum (Mo)/Cu2+ system. In this system, Mo firstly reduces Cu2+ in solution to low-valence Cu0/Cu+ on its surface. Cu0/Cu+ activates O2 to generate superoxide radical (O2•-). Importantly, O2•- can be captured immediately and oxidized to 1O2 by surface-bound Mo6+ rather than reduced to H2O2. As a result, the Mo/Cu2+ system can selectively produce 1O2. Under air and O2 conditions, the degradation efficiency of ibuprofen by Mo/Cu2+ system is 67.2 % and 76.6 %, respectively. The degradation efficiencies of bisphenol A, rhodamine B and furfuryl alcohol are 77.1 %, 87.7 % and 91.1 %, respectively. The dosages of Mo and Cu2+ are 0.4 g/L and 3 mM, respectively, and the reaction time is 2 h. Interestingly, the activity of Mo decreased by only 4.2 % after 4 cycles. Therefore, this study provides a green pathway to selectively generate 1O2 for advanced oxidation processes.

14.
J Am Chem Soc ; 144(48): 22075-22082, 2022 Dec 07.
Artigo em Inglês | MEDLINE | ID: mdl-36413924

RESUMO

Single-atom catalysts have exhibited great potential in the photocatalytic conversion of CO2 to C2 products, but generation of gaseous multi-carbon hydrocarbon products is still challenging. Previously, supports of a single atom consist of multiple elements, making C-C coupling difficult because the coordination environment of single-atom sites is diversified and difficult to control. Here, we steer C-C coupling by implanting an Au single atom on the red phosphorus (Au1/RP), support with uniform structure composed of a single element, lower electronegativity, and better ability to absorb CO2. The electron-rich phosphorus atoms near the Au single atoms can function as active sites for CO2 activation. The Au single atom can effectively reduce the energy barrier of C-C coupling, boosting the reaction kinetics of the formation of C2H6. Notably, the C2H6 selectivity and turnover frequency of Au1/RP reach 96% and 7.39 h-1 without a sacrificial agent, respectively, which almost represents the best photocatalyst for C2 chemical synthesis to date. This research will provide new ideas for the design of high-efficiency photocatalysts for CO2 conversion to C2 products.

15.
Phys Chem Chem Phys ; 24(25): 15389-15396, 2022 Jun 29.
Artigo em Inglês | MEDLINE | ID: mdl-35704391

RESUMO

Photoreduction of CO2 into CO, CH4 or hydrocarbons is attractive, due to environmental compatibility and economic feasibility. Optimizing the reaction engineering of CO2 reduction is an effective and general strategy that should be given special consideration. In this article, the photocatalytic CO2 reduction performances are originally investigated in a low vacuum in both dilute (10%) and pure CO2. We discover that the CH4 yield increased above one hundred times as the vacuum degree increased from barometric pressure to -80 kPa in dilute CO2. It also reveals long-term stability and good cycling performance in a low vacuum. The enhanced CO2 photoreduction performance in a low vacuum comes from better accumulation of photogenerated electrons, less intense Brownian movement of gas molecules in the environment and hindrance of the active site-blocking of gas molecules in the environment. Improved photocatalytic CO2 reduction in a low vacuum is further verified by Pt-TiO2 catalysts. This research presents a general route for producing clean fuels by photocatalytic CO2 reduction in a more effective way.

16.
Angew Chem Int Ed Engl ; 61(34): e202206579, 2022 Aug 22.
Artigo em Inglês | MEDLINE | ID: mdl-35715933

RESUMO

Single-atom active-site catalysts have attracted significant attention in the field of photocatalytic CO2 conversion. However, designing active sites for CO2 reduction and H2 O oxidation simultaneously on a photocatalyst and combining the corresponding half-reaction in a photocatalytic system is still difficult. Here, we synthesized a bimetallic single-atom active-site photocatalyst with two compatible active centers of Mn and Co on carbon nitride (Mn1 Co1 /CN). Our experimental results and density functional theory calculations showed that the active center of Mn promotes H2 O oxidation by accumulating photogenerated holes. In addition, the active center of Co promotes CO2 activation by increasing the bond length and bond angle of CO2 molecules. Benefiting from the synergistic effect of the atomic active centers, the synthesized Mn1 Co1 /CN exhibited a CO production rate of 47 µmol g-1 h-1 , which is significantly higher than that of the corresponding single-metal active-site photocatalyst.

17.
Chemosphere ; 303(Pt 1): 134971, 2022 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-35588886

RESUMO

Red phosphorus (P) is one of the metalloid materials, with five external electrons, it should be an excellent electron donor. However, the activity of red P to reduce Cr6+ is limited. Due to electrostatic repulsion, it is difficult for the electrons on the red P to transfer to the chromate anion (Cr6+). Interestingly, we found that Fe3+ derived from rust, waste iron or Fe3+ reagents can be used as the electron transport medium to solve the electron transport obstacles between red P and Cr6+. As a result, the reduction of Cr6+ by red P/rust system takes only 20 min, which is far lower than the 140 min of red P. The reduction rate of Cr6+ in the red P/rust system is about 12.3 times that of red P. The reaction mechanism is that red P is not easy to access chromate anions but can easily adsorb Fe3+. The adsorbed Fe3+ will be reduced to Fe2+ by red P, and the regenerated Fe2+ will diffuse into the solution to rapidly reduce Cr6+. Therefore, this work provides an alternative waste iron reuse pathway and also sheds light on the important role of electron medium in reduction reaction.


Assuntos
Cromatos , Poluentes Químicos da Água , Cromo , Transporte de Elétrons , Eletrônica , Ferro , Oxirredução , Fósforo
18.
ACS Appl Mater Interfaces ; 14(6): 7878-7887, 2022 Feb 16.
Artigo em Inglês | MEDLINE | ID: mdl-35104100

RESUMO

Hydrogen peroxide, an environmentally benign oxidant, is an effective chemical agent for water purification. On-site production of H2O2 is considered economical because it avoids the cost of storage and transportation. Traditional generation of H2O2 from oxygen reduction, as a heterogeneous electrochemical reaction, suffers from mass transfer problems because of the limited solubility and low diffusion rate of oxygen in water. These limitations can be overcome if H2O2 is formed by water oxidation. Herein, conversion of water to hydrogen peroxide was achieved efficiently on a CuWO4 anode. This water oxidation strategy can generate H2O2 at a rate of ∼11.8 µmol min-1 cm-2 at 3.0 V versus reversible hydrogen electrode. Importantly, this on-site H2O2 production shows high efficiency in water purification in O2-deficient conditions. This water oxidation anode offers a feasible way to provide a green purification agent with only water as the final byproduct, avoiding toxic intermediates and residues during the production and application.

19.
J Hazard Mater ; 425: 127996, 2022 03 05.
Artigo em Inglês | MEDLINE | ID: mdl-34902724

RESUMO

Waterborne pathogens and related diseases are a severe public health threat worldwide. Recent studies suggest that microbial interactions among infectious agents can significantly disrupt the disinfection processes, and current disinfection methods cannot inactivate intracellular pathogens effectively, posing an emerging threat to the safety of drinking water. This study developed a novel strategy, the FeP/persulfate (PS) system, to effectively inactivate intracellular bacteria within the amoeba spore. We found that the sulfate radical (SO4•-) produced by the FeP/PS system can be quickly converted into hydroxyl radicals (•OH), and •OH can penetrate the amoeba spores and inactivate the bacteria hidden inside amoeba spores. Therefore, this study proposes a novel technique to overcome the protective effects of microbial interactions and provides a new direction to inactivate intracellular pathogens efficiently.


Assuntos
Amoeba , Água Potável , Purificação da Água , Bactérias , Desinfecção , Esporos de Protozoários
20.
Chemosphere ; 278: 130376, 2021 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-33838422

RESUMO

Doping heterogeneous atoms into BiOX is recognized as an effective method to improve its photocatalytic activity. Here, S-doped BiOBr (S-BiOBr) was synthesized via a solvothermal method in the absence of water, which is supposed to substitute O as S2- in the lattice. This material is firstly used for the visible-light-driven degradation of ibuprofen, a model anti-inflammatory drug. The degradation efficiency of S-BiOBr is much higher than that of pure BiOBr. The degradation kinetic constant for S-BiOBr (2.48 × 10-2 min-1) is about 3 times as high as that of pure BiOBr (0.83 × 10-2 min-1). It is found that S-doping tunes the band structure of BiOBr, leading to a narrower band gap and thus higher utilization efficiency of visible light. The degradation of ibuprofen on S-BiOBr can be attributed to the generation of H2O2 and OH radicals. OH radical plays a synergistic role along with holes in the photocatalytic degradation process, which is supposed to be better than the reported single hole- or superoxide-dominant reaction. This work reveals a previously unrecognized and more efficient method for the degradation of organic contaminants on BiOBr.


Assuntos
Peróxido de Hidrogênio , Ibuprofeno , Bismuto , Catálise
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