Oxygen vacancy-dependent synergistic disinfection of antibiotic-resistant bacteria by BiOBr nanoflower induced H2O2 activation.

Antibiotic-resistant bacteria (ARB) and antibiotic-resistant genes (ARGs) pose a significant threat to both ecosystems and human health. Owing to the excellent catalytic activity, eco-safety, and convenience for defect engineering, BiOBr with oxygen vacancies (OVs) of different density thus were fabricated and employed to activate H2O2 for ARB disinfection/ARGs degradation in present study. We found that BiOBr with OVs of appropriate density induced via ethanol reduction (BOB-E) could effectively activate H2O2, achieving excellent ARB disinfection and ARGs degradation efficiency. Moreover, this disinfection system exhibited remarkable tolerance to complex water environments and actual water conditions. In-situ characterization and theoretical calculations revealed that OVs in BOB-E could effectively capture and activate aqueous H2O2 into HO· and O2·-. The generated reactive oxygen species combined with electron transfer could damage the cell membrane system and degrade genetic materials of ARB, leading to effective disinfection. The impressive reusability, high performance achieved in two immobilized reaction systems (packed column and baffled ditch reactor), excellent degradation of emerging organic pollutants supported the feasibility of BOB-E/H2O2 system towards practical water decontamination. Overall, this study not only provides insights into fabrication of bismuth-based catalysts for efficient ARB disinfection/ARGs degradation via OVs regulation, but also paves the way for their practical applications.

Electrochemical behavior and reaction mechanism of nano-BiOBr/rGO composite micro flower with strong interface coupling as potassium-ion battery anodes.

To explore the potential of bismuth oxybromide (BiOBr) as anodes for high-performance potassium (K)-ion batteries and understand its potassium storage mechanism, a novel nano-BiOBr/reduced graphene oxide (rGO) composite micro flower (labelled as SI-coupled nano-BiOBr/rGO micro flower), where nano-BiOBr slices are firmly anchored on rGO by strong interface coupling, is constructed. Unique microstructure accompanied by C-Bi bonds at the interface between BiOBr and rGO endows it with abundant high-speed charge transfer channels and excellent structural stability. As a result, it exhibits an excellent rate performance (a high reversible capacity of 278 mAh/g at 5 A/g) and a remarkable long-term cycling stability maintaining 95.4 % after 1000 cycles at 2.5 A/g. Furthermore, it is also found that SI-coupled nano-BiOBr/rGO micro flower anode undergoes intercalation, conversion, and alloying (BiOBr â†’ KzBiOBr â†’ Bi â†’ KBi2 â†’ K3Bi2 â†’ K3Bi) at the initial discharge process, and the subsequent charge process is only reversible dealloying and conversion reaction (K3Bi â†’ K3Bi2 â†’ KBi2 â†’ Bi â†’ BiOxBry). This work not only demonstrates the large potential of BiOBr as high-performance K-ion battery anodes, but also elucidates for the first time its K storage mechanism.

Novel eco-friendly and easily recoverable bismuth-based materials for capturing and removing polyphenols from water.

Olive oil production is one of the most developed Europe's sectors, producing olive oil and undesirable by-products, such as olive mill wastewater (OMWW) and organic waste. OMWW, containing large amounts of compounds (mainly polyphenols, phenols, and tannins), represents a problem. In fact, polyphenols have dual nature: i) antioxidant beneficial properties, useful in many industrial fields, ii) biorefractory character making them harmful in high concentrations. If not properly treated, polyphenols can harm biodiversity, disrupt ecological balance, and degrade water quality, posing risks to both environment and human health. From a circular economy viewpoint, capturing large quantities of polyphenols to reuse and removing their residuals from water is an open challenge. This study proposes, for the first time, a new path beyond the state-of-the-art, combining adsorption and degradation technologies by novel, eco-friendly and easily recoverable bismuth-based materials to capture large amounts of two model polyphenols (gallic acid and 3,4,5-trimethoxybenzoic acid), which are difficult to remove by traditional processes, and photodegrade them under solar light. The coupled process gave rise to collect 98% polyphenols, and to rapidly and effectively photodegrade the remaining portion from water.

Photocatalytically self-cleaning graphene oxide nanofiltration membranes reinforced with bismuth oxybromide for high-performance water purification.

Graphene oxide (GO) membranes have emerged as promising candidates for water purification applications, owing to their unique physicochemical attributes. Nevertheless, the trade-off between permeability and selectivity, coupled with their vulnerability to membrane fouling, poses significant challenges to their widespread industrial deployment. In this study, we introduce an innovative in-situ growth and layer-by-layer assembly technique for fabricating multilayer GO membranes reinforced with bismuth oxybromide (BiOBr) on commonly employed Nylon substrates. This method allows for the creation of two-dimensional lamellar membranes capable of photocatalytic self-cleaning and tunable nanochannel dimensions. The synthesized GO/BiOBr composite membranes exhibit remarkable water permeance rates (approximately 493.9 LMH/bar) and high molecular rejection efficiency (>99 % for Victoria Blue B and Congo Red dyes). Notably, these membranes showcase an enhanced photocatalytic self-cleaning performance upon exposure to visible light. Our work provides a viable route for the fabrication of functionalized GO-based nanofiltration membranes with BiOBr inclusions, offering a synergistic combination of high water permeability, modifiable nanochannels, and effective self-cleaning capabilities through photocatalysis.

Interior Exciton Extraction by Spatial-Controlled Iodine Doping in BiOBr Photocatalysts.

Extracting interior photoinduced species to the surface before their recombination is of great importance in pursuing high-efficiency semiconductor-based photocatalysis. Traditional strategies toward charge-carrier extraction, mostly relying on the construction of an electric field gradient, would be invalid toward the neutral-exciton counterpart in low-dimensional systems. In this work, by taking bismuth oxybromide (BiOBr) as an example, we manipulate interior exciton extraction to the surface by implementing iodine doping at the edges of BiOBr plates. Spatial- and time-resolved spectroscopic analyses verified the accumulation of excitons and charge carriers at the edges of iodine-doped BiOBr (BiOBr-I) plates. This phenomenon could be associated with interior exciton extraction, driven by an energy-level gradient between interior and edge exciton states, and the following exciton dissociation processes. As such, BiOBr-I shows remarkable performance in photocatalytic C-H fluorination, mediated by both energy- and charge-transfer processes. This work uncovers the importance of spatial regulation of excitonic properties in low-dimensional semiconductor-based photocatalysis.

Noble metals (Pd, Ag, Pt, and Au) doped bismuth oxybromide photocatalysts for improved visible light-driven catalytic activity for the degradation of phenol.

The doping of noble metals onto the semiconductor metal oxides has a great impact on the intrinsic properties of the materials. This present work reports the synthesis of noble metals doped BiOBr microsphere by a solvothermal method. The various characteristic findings reveal the effective incorporation of Pd, Ag, Pt, and Au onto the BiOBr and the performance of synthesized samples was test for the degradation of phenol over visible light. The Pd-doped BiOBr material showed enhanced phenol degradation efficacy, which is ∼4-fold greater than pure BiOBr. This improved activity was on reason of good photon absorption, lower recombination rate, and higher surface area facilitated by surface plasmon resonance. Moreover, Pd-doped BiOBr sample displayed good reusability and stability after 3 cycles of run. A plausible charge transfer mechanism for phenol degradation is disclosed in detail over Pd-doped BiOBr sample. Our findings disclose that the incorporation of noble metal as the electron trap is a feasible approach to enhance visible light activity of BiOBr photocatalyst used in phenol degradation. This work represents new vision interested in the outline and development of noble metal doped semiconductor metal oxides as a visible light material for the elimination of colorless toxins from untreated wastewater.

Construction of PDIsa/BiOBr type-I scheme heterojunction for efficient ciprofloxacin photocatalytic degradation.

Fabrication of heterojunction photocatalysts is a promising strategy for enhancing photocatalytic activity. However, the study about traditional type-I heterojunction still remains to be developed. Herein, a PDIsa/BiOBr traditional type-I heterojunction was constructed by electrostatic self-assembly method, which owned improved light absorption capacity and photogenerated charge separation efficiency. The interfacial electric field and the polarization electric field of PDIsa impelled the separation of excitons. The degradation rate of ciprofloxacin (CIP) was improved by 3.2 times over the optimal PDIsa/BiOBr composite than pure BiOBr. In addition, the TOC removal efficiency reached 67.34% within 120 min. Trapping experiments and electron spin resonance (ESR) tests showed that superoxide radical (•O2-) was the most active species, and singlet oxygen (1O2) and hole (h+) played a secondary role. The work may furnish a new reference for designing BiOBr-based type-I heterojunction.

Enhanced visible-light driven photocatalytic degradation of bisphenol A by tuning electronic structure of Bi/BiOBr.

Visible-light (VL) photocatalysis has been regarded as an intriguing technology for the control of persistent environmental pollutants. In this study, the novel homogeneous Co doped-Bi/BiOBr nanocomposites (CB-X) were prepared via a facile one-step hydrothermal method, featured with a uniform 0D Bi nanodots distribution on 2D Co-doped BiOBr nanosheets, and the photocatalytic performance was evaluated by decomposing the BPA as a prototype contaminant. The degradation experiment indicated that the optimal CB-2 nanocomposite exhibited the best photocatalytic activity with a 94% removal efficiency of BPA under the VL irradiation of 30 min; And the corresponding apparent rate constant (k) was as high as 0.107 min-1, which was 10.7 times greater than that of Bi/BiOBr (0.010 min-1). Benefiting from the modulation effect of Co-doping on the intrinsic electron configuration of Bi/BiOBr, the elevated VL adsorption capacity and accelerated h+/e- pairs separation rate were achieved, which were evidenced by photoluminescence (PL) spectroscopy, photo-electrochemical measurements and density functional theory (DFT) calculation. Moreover, the major reactive species in CB-X/VL system were uncovered to be •O2- and 1O2, whereas •OH and h+ presented a secondary contribution in the BPA elimination. Finally, the possible photocatalytic mechanism involved in CB-X nanocomposites and BPA degradation pathways were proposed on the basis of the various intermediates and products detected by LC-MS/MS.

Interface engineering of p-p Z-scheme BiOBr/Bi12O17Br2 for sulfamethoxazole photocatalytic degradation.

The Z-scheme heterojunction has received widespread attention due to it can effectively improve the photocatalytic activity of photocatalytic materials. In this paper, a p-p Z-scheme hererojunction composed of bismuth oxybromide and oxygen-rich bismuth oxybromide was synthesized via facile one-step solvothermal method. Based on the characterization results, we demonstrated that the BiOBr/Bi12O17Br2 Z-scheme heterojunction was synthesized by intimate interface contact between BiOBr and Bi12O17Br2 p-type semiconductors. This endowed the heterojunction composite with excellent photogenerated carrier transfer ability and photogenerated electron-hole separation performance compared with pure BiOBr and Bi12O17Br2 materials, which were proven by photoelectrochemical measurement, photoluminescence spectra. The maximum photocurrent of BiOBr/Bi12O17Br2 (≈0.32 µA) is approximately 3 times that of the original BiOBr (≈0.08 µA ) when light is irradiated. In addition, the BiOBr/Bi12O17Br2 p-p Z-scheme composite photocatalyst had good photocatalytic activity for sulfamethoxazole, with ·O2- free radicals as the main active species. It could photodegrade 99% sulfamethoxazole under light irradiation at 365 nm, and its degradation rate was approximately 13 times that of BiOBr and 1.5 times that of Bi12O17Br2 materials. Notably, BiOBr/Bi12O17Br2 exhibited an excellent performance after 4 consecutive runs. Besides, the possible degradation pathway of sulfamethoxazole was proposed. This work has reference significance for the construction of p-p Z-scheme heterojunctions and the treatment of environmental contaminants.

Visible-Light-Driven Ag-Doped BiOBr Nanoplates with an Enhanced Photocatalytic Performance for the Degradation of Bisphenol A.

Based on the low utilization rate of visible light and the high-charge carriers-recombination efficiency of bismuth oxybromide (BiOBr), in this work, noble metal Ag was used to modify BiOBr, and Ag-doped BiOBr nanoplates (Ag-BiOBr) were obtained through a one-step hydrothermal method. Compared with BiOBr, the absorption edge of Ag-BiOBr showed a redshift from 453 nm to 510 nm, and the absorption efficiency of visible light was, obviously, improved. Bisphenol A (BPA) was chosen as the target pollutant, to evaluate the photocatalytic performance of the samples. Ag0.1-BiOBr showed the highest degradation efficiency. The intrinsic photocatalytic activity of Ag0.1-BiOBr, under visible light, was approximately twice as high as that of BiOBr. In this way, a new visible-light-driven photocatalyst was proposed, to fight against organic pollution, which provides a promising strategy for water and wastewater treatment.

Efficient photocatalytic degradation of emerging ciprofloxacin under visible light irradiation using BiOBr/carbon quantum dot/saponite composite.

The use of visible-driven photocatalysts has fascinated attention as a capable and sustainable approach for wastewater remediation. In this work, BiOBr/carbon quantum dot (CQDs)/saponite composites (CQDs/Clay@BiOBr) were fabricated via hydrothermally using two different CQDs/Clay precursors (in-situ synthesis (IS) and physical mixing (PM)). The obtained products were characterized, and the photocatalytic performances of the prepared samples were evaluated in the photocatalytic decomposition of emerging ciprofloxacin (CIP) pharmaceutical waste. The highest CIP mineralization performance was achieved when a combination of BiOBr and CQDs/Clay (IS) with the appropriate proportion because the strong adhesion between CQDs and clay generate a great heterojunction in the composite. The stronger interaction of CQDs and better distribution of CQDs on the surface of clay in the CQDs/Clay (IS) enhanced the interaction of BiOBr and CQDs, and avoided the re-agglomeration of excess of CQDs on surface of BiOBr which reduce the active surface to receive the light and react with CIP. The ultrafast degradation rate of the optimized CQDs/Clay@BiOBr composite was better compared to others. The significant improvement in the CIP degradation efficiency of the CQDs/Clay@BiOBr composite was attributed to the excellent separation and transportation of photogenerated electrons and holes, as confirmed by photoluminescence, photocurrent density, and electrochemical impedance spectroscopy results. Moreover, the photocatalytic degradation mechanism of CIP in the CQDs/Clay@BiOBr composite was proposed based on the electronic states of each material in the composite and on a scavenger test. Thus, the proposed CQDs/Clay@BiOBr composite can be employed as a potential visible-light-driven photocatalyst for the decomposition of organic contaminants in wastewater.

Preparation, Characterization and Application of Epitaxial Grown BiOBr (110) Film on ZnFe2O4 Surface with Enhanced Photocatalytic Fenton Oxidation Properties.

A novel BiOBr photocatalyst was epitaxially grown in situ onto the surface of ZnFe2O4, a ferroelectric material with a strong polarization effect. The formatted BiOBr/ZnFe2O4 composite (BOB/ZFO) showed excellent photocatalytic degradation performance of tetracycline antibiotics (TCs). One of the composites with ZnFe2O4 content of 10% (BOB/ZFO-10) showed the best properties; the degradation efficiency of TCs upon visible light irradiation for 180 min was 99.2%, which was 3.58 times higher than that of pure phase BiOBr. The functions of ZnFe2O4 are assumed to be such that the addition of this ferroeletric material not only regulated the spontaneous polarization of BiOBr in the process of synthesis, but also resulted in the construction of Z-scheme heterostructures due to the appropriate staggered band structure of BiOBr and ZnFe2O4. In the presence of ferroelectric material ZnFe2O4, the local structure of BiOBr may be distorted accordingly, resulting in preferential growth of a (110) crystal facet of BiOBr and enhancement of spontaneous polarization, which promotes the efficient separation of photogenerated electron-hole pairs of ZnFe2O4 and BiOBr, and therefore enhances the redox capacity of the photocatalytic degradation of organic pollutants.

Electron-Level Mechanistic Insights into Ce Doping for Enhanced Efficiency Degradation of Bisphenol A under Visible Light Irradiation.

Bismuth oxybromide (BiOBr), with its special layered structure, is known to have potential as a visible-light-driven photocatalyst. However, the rapid recombination and short lifetime of the photogenerated carriers of BiOBr restrict its photocatalytic efficiency for the degradation of organic pollutants. Given the similar ionic size of Ce and Bi, Ce atoms might be easily introduced into the crystal of BiOBr to tailor its band structure. In this study, Ce doped BiOBr (Ce-BiOBr) samples with different percentages of Ce contents were prepared via a hydrothermal method. The intrinsic photocatalytic efficiency of Ce0.2-BiOBr for the degradation of bisphenol A (BPA) was 3.66 times higher than that of pristine BiOBr under visible light irradiation. The mechanism of Ce-doping modification for the enhanced photocatalytic performance was demonstrated based on a series of experiments and DFT calculation. The narrowed bandgap, the enhanced charge separation efficiency and Ce-doping energy level contributed to the remarkable photocatalytic performance of Ce-BiOBr.

Efficient charge separation and improved photocatalytic activity in Type-II & Type-III heterojunction based multiple interfaces in BiOCl0.5Br0.5-Q: DFT and Experimental Insight.

The nanostructured, inner-coupled Bismuth oxyhalides (BiOX0.5X'0.5; X, X' = Cl, Br, I; X≠X') heterostructures were prepared using Quercetin (Q) as a sensitizer. The present study revealed the tuning of the band properties of as-prepared catalysts. The catalysts were characterized using various characterization techniques for evaluating the superior photocatalytic efficiency and a better understanding of elemental interactions at interfaces formed in the heterojunction. The material (BiOCl0.5Br0.5-Q) reflected higher degradation of MO (about 99.85%) and BPA (98.34%) under visible light irradiation than BiOCl0.5I0.5-Q and BiOBr0.5I0.5-Q. A total of 90.45 percent of total organic carbon in BPA was removed after visible light irradiation on BiOCl0.5Br0.5-Q. The many-fold increase in activity is attributed to the formation of multiple interfaces between halides, conjugated π-electrons and multiple -OH groups of quercetin (Q). The boost in degradation efficiency can be attributed to the higher surface area, 2-D nanostructure, inhibited electron-hole recombination, and appropriate band-gap of the heterostructure. Photo-response of BiOCl0.5Br0.5-Q is higher compared to BiOCl0.5I0.5-Q and BiOBr0.5I0.5-Q, indicating better light absorption properties and charge separation efficiency in BiOCl0.5Br0.5-Q due to band edge position. First-principles Density Functional Theory (DFT) based calculations have also provided an insightful understanding of the interface formation, physical mechanism, and superior photocatalytic performance of BiOCl0.5Br0.5-Q heterostructure over other samples.

One-Step Microwave-Assisted Synthesis and Visible-Light Photocatalytic Activity Enhancement of BiOBr/RGO Nanocomposites for Degradation of Methylene Blue.

In this study, bismuth oxybromide/reduced graphene oxide (BiOBr/RGO), i.e. BiOBr-G nanocomposites, were synthesized using a one-step microwave-assisted method. The structure of the synthesized nanocomposites was characterized using Raman spectroscopy, X-ray diffractometry (XRD), photoluminescence (PL) emission spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FTIR), and ultraviolet-visible diffuse reflection spectroscopy (DRS). In addition, the ability of the nanocomposite to degrade methylene blue (MB) under visible light irradiation was investigated. The synthesized nanocomposite achieved an MB degradation rate of above 96% within 75 min of continuous visible light irradiation. In addition, the synthesized BiOBr-G nanocomposite exhibited significantly enhanced photocatalytic activity for the degradation of MB. Furthermore, the results revealed that the separation of the photogenerated electron-hole pairs in the BiOBr-G nanocomposite enhanced the ability of the nanocomposite to absorb visible light, thus improving the photocatalytic properties of the nanocomposites. Lastly, the MB photo-degradation mechanism of BiOBr-G was investigated, and the results revealed that the BiOBr-G nanocomposites exhibited good photocatalytic activity.

Controlled hydrothermal synthesis of BiOxCly/BiOmBrn/g-C3N4 composites exhibiting visible-light photocatalytic activity.

The first systematic synthesis of bismuth oxychloride/bismuth oxybromide/graphitic carbon nitride (BiOxCly/BiOmBrn/g-C3N4) nano-composites used a controlled hydrothermal method. The structure, morphology and characteristic of BiOxCly/BiOmBrn/g-C3N4 photocatalyst were measured by XRD, UV-vis-DRS, FT-IR, FE-TEM, FE-SEM-EDS, PL, BET, HR-XPS and EPR. Under visible light irradiation, the photodegradation activity was evaluated for the decolorization of crystal violet (CV) and 2-hydroxybenzoic acid (2-HBA) in aqueous solution. The catalytic performance showed that, when using sample BB2C1-4-250-30 wt% g-C3N4 composite as a photocatalyst, the best reaction-rate-constant (k) was 0.071 h-1. It was 1.5 times higher than the k value of BB2C1-4-250 as a photocatalyst. From the scavenging effect of various scavengers, the results of EPR showed that reactive OH was the main scavenger, while O2-, h+ and 1O2 were the second scavenger in CV degradation. In this study, a possible photodegradation mechanism was proposed and discussed. In this work, our method of BiOxCly/BiOmBrn/g-C3N4 preparation could be used for future mass production and the BiOxCly/BiOmBrn/g-C3N4 composite materials could be applied to the environmental pollution control in future.

Novel S-doped BiOBr nanosheets for the enhanced photocatalytic degradation of bisphenol A under visible light irradiation.

Bisphenol A (BPA), a typical endocrine disrupting chemical, is widespread in aqueous environment and cannot be efficiently treated by traditional water treatment technologies. Bismuth oxybromide (BiOBr) is a promising photocatalyst with a special layered structure. However, its band gap (2.8 eV) is not narrow enough for the efficient harvesting of visible light, severely restricting its practical use. Given that the band gap of Bi2S3 is only 1.3 eV, S-doping modification could be used to tailor the band structure of BiOBr. Here, series of S-doped BiOBr nanosheets was prepared through a facile hydrothermal procedure. The as-prepared S0.2-BiOBr nanosheets showed a narrower band gap of 2.33 eV. The intrinsic photocatalytic activity of S0.2-BiOBr sample for the degradation of BPA was 2.78 times higher than that of BiOBr under visible light degradation. Moreover, the mechanism of BPA degradation over the S-doped BiOBr under visible light irradiation was elucidated based on the experimental results and density functional theoretical calculations. Overall, a feasible and effective doping method was proposed to improve the utilization efficiency of visible light.

Fabrication of leaf extract mediated bismuth oxybromide/oxyiodide (BiOBrxI1-x) photocatalysts with tunable band gap and enhanced optical absorption for degradation of organic pollutants.

The use of Azadirachta indica (A.I.) leaf extract to synthesize green photocatalysts for efficient separation of photogenerated charges has been a promising way to enhance the photocatalytic activity. Herein, we report the synthesis of green bismuth oxybromide/oxyiodide composites (G-BiOBrxI1-x) using A.I. leaf extract with effective size control, high specific surface area, and porosity. The A.I. leaf extract also acted as an excellent sensitizer that boosted the optical window of the G-BiOBrxI1-x photocatalysts. The as-prepared G-BiOBrxI1-x photocatalysts possessed three-dimensional (3-D) nanoplates like structure with successive modulation of the band gaps from 2.28 eV to 1.98 eV by varying the bromine/iodine (Br/I) ratio. Furthermore, the photocatalytic activity of the G-BiOBrxI1-x samples was measured and compared with the bismuth oxybromide/oxyiodide composite (C-BiOBr0.5I0.5) synthesized via conventional hydrolysis route (without the leaf extract). The G-BiOBrxI1-x photocatalysts degraded higher percentage of methyl orange (MO) and amoxicillin (AMX) than C-BiOBr0.5I0.5 under visible light irradiation. The superior photocatalytic efficiency was attributed to the multiple heterojunctions developed between BiOBr, BiOI, and electron-accepting π-conjugated system offered by leaf extract constituents, thereby facilitating the charge transfer process and effective separation of photogenerated charges.

Oxygen Vacancy Engineering Promoted Photocatalytic Ammonia Synthesis on Ultrathin Two-Dimensional Bismuth Oxybromide Nanosheets.

The catalytic conversion of nitrogen to ammonia is one of the most important processes in nature and chemical industry. However, the traditional Haber-Bosch process of ammonia synthesis consumes substantial energy and emits a large amount of carbon dioxide. Solar-driven nitrogen fixation holds great promise for the reduction of energy consumption and environmental pollution. On the basis of both experimental results and density functional theory calculations, here we report that the oxygen vacancy engineering on ultrathin BiOBr nanosheets can greatly enhance the performance for photocatalytic nitrogen fixation. Through the addition of polymetric surfactant (polyvinylpyrrolidone, PVP) in the synthesis process, VO-BiOBr nanosheets with desirable oxygen vacancies and dominant exposed {001} facets were successfully prepared, which effectively promote the adsorption of inert nitrogen molecules at ambient condition and facilitate the separation of photoexcited electrons and holes. The oxygen defects narrow the bandgap of VO-BiOBr photocatalyst and lower the energy requirement of exciton generation. In the case of the specific surface areas are almost equal, the VO-BiOBr nanosheets display a highly improved photocatalytic ammonia production rate (54.70 µmol·g-1·h-1), which is nearly 10 times higher than that of the BiOBr nanoplates without oxygen vacancies (5.75 µmol·g-1·h-1). The oxygen vacancy engineering on semiconductive nanomaterials provides a promising way for rational design of catalysts to boost the rate of ammonia synthesis under mild conditions.

Facile Green Synthesis of BiOBr Nanostructures with Superior Visible-Light-Driven Photocatalytic Activity.

Novel green bismuth oxybromide (BiOBr-G) nanoflowers were successfully synthesized via facile hydrolysis route using an Azadirachta indica (Neem plant) leaf extract and concurrently, without the leaf extract (BiOBr-C). The Azadirachta indica leaf extract was employed as a sensitizer and stabilizer for BiOBr-G, which significantly expanded the optical window and boosted the formation of photogenerated charge carriers and transfer over the BiOBr-G surface. The photocatalytic performance of both samples was investigated for the degradation of methyl orange (MO) and phenol (Ph) under the irradiation of visible light. The leaf extract mediated BiOBr-G photocatalyst displayed significantly higher photocatalytic activity when compared to BiOBr-C for the degradation of both pollutants. The degradation rate of MO and Ph by BiOBr-G was found to be nearly 23% and 16% more when compared to BiOBr-C under visible light irradiation, respectively. The substantial increase in the photocatalytic performance of BiOBr-G was ascribed to the multiple synergistic effects between the efficient solar energy harvesting, narrower band gap, high specific surface area, porosity, and effective charge separation. Furthermore, BiOBr-G displayed high stability for five cycles of photocatalytic activity, which endows its practical application as a green photocatalyst in the long run.