Light Harvesting Research Articles

High-Efficiency Solar Transformation of Sugars via a Heterogenous Gallium(III) Catalyst.

Extremely limited research exploring the photocatalytic potential of main group metals, such as aluminum, gallium, and tin, has been undertaken due to their weak light harvesting properties. This study reports the efficient transformation of sugars to 5-hydroxymethylfurfural (HMF) with high yield employing an original heterogeneous photocatalyst comprising a gallium(III) complex immobilized on an alumina support. Under visible light irradiation, the reaction rate of HMF formation is ~143 times higher than the equivalent thermal reaction performed in the absence of light. The turnover number (TON) of the heterogeneous gallium(III) photocatalyst was as high as 1500, which was ca. two orders of magnitude higher than the TON of the homogeneous gallium(III) system. It is proposed that photoirradiation significantly enhances the Lewis acidity of the catalyst by forming a semi-coordination state between gallium(III) and N-donor ligands, enabling the increased interaction of reactant sugar molecules with gallium(III) active sites. Consistent with this, the photoresponsive coordination of the gallium(III) complex and the abstraction of the hydroxy group by the metal under irradiation with visible light is observed by NMR spectroscopy for the first time. These findings demonstrate that efficient photocatalysts derived from the main group elements can facilitate biomass conversion using visible light.

High‐Efficiency Solar Transformation of Sugars via a Heterogenous Gallium(III) Catalyst

AbstractExtremely limited research exploring the photocatalytic potential of main group metals, such as aluminum, gallium, and tin, has been undertaken due to their weak light harvesting properties. This study reports the efficient transformation of sugars to 5‐hydroxymethylfurfural (HMF) with high yield employing an original heterogeneous photocatalyst comprising a gallium(III) complex immobilized on an alumina support. Under visible light irradiation, the reaction rate of HMF formation is ~143 times higher than the equivalent thermal reaction performed in the absence of light. The turnover number (TON) of the heterogeneous gallium(III) photocatalyst was as high as 1500, which was ca. two orders of magnitude higher than the TON of the homogeneous gallium(III) system. It is proposed that photoirradiation significantly enhances the Lewis acidity of the catalyst by forming a semi‐coordination state between gallium(III) and N‐donor ligands, enabling the increased interaction of reactant sugar molecules with gallium(III) active sites. Consistent with this, the photoresponsive coordination of the gallium(III) complex and the abstraction of the hydroxy group by the metal under irradiation with visible light is observed by NMR spectroscopy for the first time. These findings demonstrate that efficient photocatalysts derived from the main group elements can facilitate biomass conversion using visible light.

Porphyrin-based nanoporous materials for photocatalytic applications

Alongside the unique photophysical properties, porphyrin derivatives play key roles in light harvesting of photosynthetic organisms. Due to their symmetrical structure, porphyrin derivatives serve as excellent building blocks for various porous materials, encompassing metal-organic frameworks, covalent organic frameworks, hydrogen-bonded organic frameworks, and amorphous porous organic polymers. These materials capitalize on the beneficial characteristics of porphyrins, such as their absorption capabilities, redox activity, and coordination chemistry, while leveraging the surface area and porosity inherent in porous frameworks. Porphyrin-based porous materials are explored for diverse applications including gas storage, energy storage, catalysis, separation, sensing, and environmental remediation. Owing to their excellent photophysical properties, these nanoporous materials are suitable for light harvesting and photocatalysis applications. This review emphasizes the potential of artificial light-harvesting catalysts based on porphyrin-based porous materials for solar energy applications. Researchers aim to optimize material properties and design innovative architectures to enhance performance in solar energy conversion and photocatalytic applications, making this a rapidly evolving field. Specific applications discussed in the review include photocatalytic CO2 reduction, photocatalytic water splitting, and perspectives on future developments in the field of porphyrin-based nanoporous materials for artificial light harvesting.

The Unusual Functional Role of Protein Flexibility in Photosynthetic Light Harvesting: Protein Dynamics Studied Using Neutron Scattering

In addition to investigations of the three-dimensional protein structure, information on the dynamical properties of proteins is indispensable for an understanding of protein function in general. Correlations between protein dynamics and function are typically anticipated when both molecular mobility and function are concurrently affected under specific temperatures or hydration conditions. In contrast, excitation energy transfer within the major photosynthetic light-harvesting complex II (LHC II) presents an atypical case, as it remains fully operational even at cryogenic temperatures, primarily depending on the interactions between electronic states and involving harmonic protein vibrations only. This review summarizes recent work on vibrational and conformational protein dynamics of LHC II and directly relates these findings to its light-harvesting function. In addition, we give a comprehensive introduction into the use of neutron spectroscopy and molecular dynamics simulations to investigate the protein dynamics of photosynthetic protein complexes in solution, which is information complementary to that obtained by protein crystallography.

An Unexpected Water Channel in the Light-Harvesting Complex of a Diatom: Implications for the Switch between Light Harvesting and Photoprotection

An Unexpected Water Channel in the Light-Harvesting Complex of a Diatom: Implications for the Switch between Light Harvesting and Photoprotection

Performance enhancement of dye solar cell using mixed synthetic organic dyes

The potential of dyes derived from Bromophenol and Rhodamine, both as single and mixed dyes, in dye-sensitized solar cells (DSSCs) to achieve panchromatic light harvesting and enhance cell performance is assessed in this study. The study finds that a high molar extinction coefficient caused by the combined properties of the dyes matched with the spectrum area where the novel sensitizers deficit light-harvesting, indicating effective co-sensitization. To ascertain the dyes' characteristics and appropriateness as sensitizers, a variety of methods, including cyclic voltammetry, UV–Vis spectroscopy, and Fourier-transform infrared spectroscopy (FTIR), are used. Cyclic voltammetry results indicate that the dyes under study exhibit excellent redox stability and sufficient thermodynamic dynamic force for efficient electron introduction. According to the photovoltaic performance statistics, the mixed dye of Rhodamine and Bromophenol based cell had the maximum efficiency (η) and power (Jsc) are 4.06 mA and 1.29 %, respectively. This is made feasible by photosensitive light-harvesting, remarkable visual activity, and sufficient energy levels. Acidified mixed dyes were more able to load on the TiO2 surface due to their homogenous dispersion, reduced steric barriers, and multi-anchor group connected to the semiconductor surface. With such novel mixed dye, it is expected that the mixed dye with not only high efficiency but higher Jsc value will be an alternative to single dyed based DSSCs.

Integrating Mo2C/C as cocatalyst into S-scheme Mo2C/C/Co0.5Cd0.5S heterojunction with spatial photocarrier separation for photocatalytic synergistic H2 evolution

Reasonable design and production of potent photocatalysts for sustainable H2 production from solar energy is one of the necessary strategies in the photocatalysis process. The S-scheme heterojunction exposes remarkable superiority in boosting light harvesting and progressing photocarrier separation efficiency in the photocatalyst. Here, new S-scheme heterojunction Mo2C/C/Co0.5Cd0.5S photocatalysts, including different weights of noble metal-free Mo2C/C nanostructures as cocatalysts, were successfully synthesized. As expected, the nanocomposite structures exhibited increased photocatalytic activity relative to single Co0.5Cd0.5S. The nanocomposite containing 5 wt% Mo2C/C exhibited an increased hydrogen production efficiency of 83.86 mmol g−1 h−1, which was 8.4 times higher than single Co0.5Cd0.5S (10.06 mmol g−1 h−1). This implies that for Co0.5Cd0.5S, Mo2C/C increases visible light absorption, facilitates photocarrier separation, and boosts the H2 evolution rate. Moreover, conductive carbon nanoparticles, electron mediators with strong interfacial interaction, serve as rapid photocarrier transfer bridges between Co0.5Cd0.5S and Mo2C. In summary, the superb efficiency of Mo2C/C/Co0.5Cd0.5S is accredited to the synergistic effect between Co0.5Cd0.5S and Mo2C/C, the creation of S-scheme heterojunction, which assists the separation of photocarriers and declines the recombination possibilities. This research ensures a reference and new profound insight for understanding and designing noble metal-free cocatalyst-assisted S-scheme heterojunctions for immensely efficient photocatalytic H2 production.

Device optimization of all inorganic CsPbBr3/LNMO based multi-layered perovskite light harvesters for broader capturing of solar spectrum

All inorganic Cesium lead bromide (CsPbBr3) planar perovskites have garnered enormous significance in photovoltaic applications owing to its outstanding stability against oxygen, heat and moisture. However, the power conversion efficiencies of the CsPbBr3 planar perovskites are quite low primarily due to the inferior range of light absorbance and interfacial charge recombination losses. This issue can be successfully resolved with a novel multi-absorber architecture approach which incorporates dual absorbers consisting of a lower band gap Lanthanum Nickel Manganese Oxide (La2NiMnO6 or LNMO) material along with the wider band gap CsPbBr3 material so that the light absorbance regime could be well extended for maximal utilization of the solar spectrum. Therefore, this article incorporates numerical modeling and guided optimization of all inorganic ITO/ETL/CsPbBr3/La2NiMnO6(LNMO)/HTL dual absorbers-based heterojunction structure to improvise the power conversion efficiency of CsPbBr3 based single absorber PSCs. The critical device’s parameters, such as; absorber layer and carrier transport layer thickness, defect density, temperature, doping concentration, frequency response, capacitance effects, Mott-Schottky effects as well as series and shunt resistances are thoroughly optimized and evaluated using Solar Cell Capacitance Simulator (SCAPS-1D) simulator. The proposed dual absorber layer composition produces a substantial enhancement in performance with a peak power conversion efficiency (PCE) of 26.98 %, short circuit current (Jsc) of 39.75 mA/cm2, open circuit voltage (Voc) of 0.85 V, and fill factor (FF) of 77.98 % at a device defect density of 1015 cm−3 outperforming the 11 % of PCE attained with the experimentally reported CsPbBr3 single junction counterpart along with PSCs with various dual absorbers-based composition.

Unearthing the Real-Time Excited State Dynamics from Antenna to Rare Earth Ions Using Ultrafast Transient Absorption.

The conventional energy transfer pathway in organic lanthanide complexes is purported to be from the excited singlet state of the chromophore to the triplet state and subsequently directly to the emitting state of the trivalent lanthanide ion. In this work, we found that the energy transfer occurs from the triplet state to the nearest energy level, instead of directly to the emitting state of the lanthanide ion. The triplet decay rate for different lanthanide ions follows an energy gap law from the triplet level to the receiving level of the lanthanide ion. Three different categories of complexes were synthesized and inspected using different techniques, demonstrating the universality of our findings. This work renews the insights to conventional findings, highlighting the importance of the energy gap between the triplet state and the nearest lanthanide energy level in optimization of light harvesting. The rationale of ligand design of chromophores should be reconsidered, leading to various applications of lanthanide complexes with enhanced quantum yield and brightness.

Effect of doping level on the photoconduction and chemiresistive ethanol gas sensing of lanthanum-doped CuO films

Undoped and lanthanum (La)-doped copper oxide (CuO) thin films were prepared by the nebulizer spray pyrolysis technique. The X-ray diffraction analysis revealed that the effective doping of lanthanum does not alter the monoclinic crystalline structure of copper oxide thin films. Raman spectra confirmed the crystalline quality of undoped and La-incorporated CuO films. From, scanning electron micrograph images, the La-doped CuO films exhibit spherical particles. Energy dispersive X-ray analysis confirmed the existence of copper, lanthanum and oxygen elements. The doping of La-substituted CuO films showed a minimum bandgap when compared to undoped CuO film. The oxidation states of Cu 2p, La 3d and O 1s elements were observed. The electrical resistivity of the films was considerably decreased due to the doping of La ions in CuO matrix. The photoluminescence spectra show that the doping of La ions increases the defect states and shows increased intensity. The time resolved photoluminescence analysis revealed that an extended carrier lifetime was observed for the La-doped films. The La-doped CuO sensors achieved a superior gas sensing performance at room temperature and exhibited quick response and recovery times, suggesting that the sensor has the potential for the detection of harmful volatile gases in real-world applications. The photoconductive investigation revealed that the La-doped CuO films exhibited higher charge-transporting properties and increased light-harvesting ability. This study sheds light on designing gas sensors working under ambient conditions and photosensors for optoelectronic devices.

Attached meso-tetra (4-carboxyphenyl) porphyrin copper (II) to BiOCl for enhanced photocatalytic performance in antibiotics degradation

Bismuth oxychloride (BiOCl) has been considerably accepted as a photocatalyst due to its excellent photoelectrochemical properties, low cost and corrosion resistance. However, its further application has not progressed due to limited visible-light utilization and quick recombination of photoexcited carriers. In this work, a series of meso-tetra (4-carboxyphenyl) porphyrin copper (II) (CuTCPP) hybridized BiOCl composites (CuTCPP/BiOCl) were synthesized to use as an efficient visible-light responsive photocatalyst for the degradation of antibiotics pollutants in the wastewater systems. The characterization results confirmed that the 2D fusiform-shaped CuTCPP nanosheets were successfully inserted into hierarchical flower-like BiOCl. The photocatalytic degradation of several typical antibiotics (tetracycline, enrofloxacin and ciprofloxacin) demonstrated that CuTCPP/BiOCl showed better photocatalytic activities than pure BiOCl. Further, 0.5 wt% CuTCPP/BiOCl manifested the optimal photocatalytic efficiency for decomposing the antibiotics, and its degradation rate constant was about 2.84 times higher than that of pristine BiOCl. The significantly improved photocatalytic performance was mainly due to the promotion of visible light harvesting and enhanced separation of photogenerated carriers after the introduction of the macrocyclic CuTCPP. The radical substances determination confirmed that active •O2−, h+ and •OH existed in the photocatalytic removal of antibiotic, in which •O2− was the main reactive oxidizing species. The excellent degradation efficiency of CuTCPP/BiOCl reveals its great potential as photocatalysts for use in the alleviation of antibiotic contaminants and wastewater purification.

Shining a light on Co(terpyridine)2 complexes: Unravelling the impact of ligand substitution at the 4’-position on optical and electrochemical properties through experimental and theoretical investigations

The present work involves synthesis, characterisation and study of absorption, emission and electrochemical properties of cobalt(III) bis-terpyridine complexes with varying substituent at the 4’-position of the central pyridine ring of terpyridine moiety. The work clearly demonstrates the modulation of the light harvesting window with changing the substituent viz. phenyl, naphthalenyl and thienyltriphenylamine. The naphthalenylterpyridine based cobalt complex shows considerable room temperature luminescence. Cyclic voltammetry data of the complexes reveal a reversible CoIII/II based redox feature. DFT based structure optimisations for all the complexes were performed at the B3LYP level using 6-31G (d,p) and LANL2DZ basis sets. TD-DFT based theoretical calculations were performed with the optimised structures to simulate the experimental absorption spectrum for all the complexes and hence the electronic transitions for the observed absorption peaks were assigned.

ZnCo2O4@g-C3N4@Cu as a new and highly efficient heterogeneous photocatalyst for visible light-induced cyanation and Mizoroki-Heck cross-coupling reactions.

Conducting C-C cross-coupling reactions under convenient and mild conditions remains extremely challenging in traditional organic synthesis. In this study, ZnCo2O4@g-C3N4@Cu exhibited extraordinary photocatalytic performance as a new visible light harvesting heterogeneous copper-based photocatalyst in cyanation and Mizoroki-Heck visible-light-driven cross-coupling reactions at room temperature and in air. Surprisingly, by this method, the cyanation and Mizoroki-Heck cross-coupling reactions of various iodo-, bromo- and also the challenging chloroarenes with respectively K4[Fe(CN)6]·3H2O and olefins produced promising results in a sustainable and mild media. The significant photocatalytic performance of ZnCo2O4@g-C3N4@Cu arises from the synergistic optical properties of ZnCo2O4, g-C3N4, and Cu. These components can enhance the charge carrier generation and considerably reduce the recombination rate of photogenerated electron-hole pairs. No need to use heat or additives, applying an economical and benign light source, utilizing an environmentally compatible solvent, facile and low-cost photocatalytic approach, aerial conditions, high stability and convenient recyclability of the photocatalyst are the remarkable highlights of this methodology. Moreover, this platform exhibited the ability to be performed on a large scale, which is considered an important issue in industrial and pharmaceutical use. It is worth noting that this is the first time that a heterogeneous copper-based photocatalyst has been employed in visible light-promoted cyanation reactions of aryl halides.

Hybrid NenG/ZSM‐5 Towards Highly Selective and Efficient Photocatalysis for Generation of Leucodopaminechrome and Gluconic Acid Under Solar Light

AbstractGlucose, an abundant and renewable form of biomass, has garnered significant attention in research for its conversion into high‐value chemicals such as gluconic acid. Traditional methods for biomass transformation typically involve high energy input, elevated temperature, pressure, and costly systems. In contrast, photocatalysis emerges as a promising approach to produce organic molecules under mild conditions, harnessing energy from natural sunlight or lamps. This study presents the nitrogen‐enriched graphene with zeolite second Mobil–5 (NenG/ZSM‐5) photocatalyst, evaluated for generating high‐value chemicals (gluconic acid and leucodopaminechrome) under solar light irradiation. The NenG/ZSM‐5 photocatalyst, synthesized from nitrogen‐doped graphene and ZSM‐5, successfully converted dopamine into leucodopaminechrome (71.54 %) — a critical step in dopamine regeneration and transformed glucose into gluconic acid (85 %). The addition of ZSM‐5 to NenG provided stability and enhanced product selectivity. The outstanding performance of the NenG/ZSM‐5 photocatalyst can be attributed to its heightened solar light harvesting potential, appropriate energy band gap, and uniformly arranged π‐electron channels. This research focuses on solar conversion of glucose to gluconic acid and dopamine regeneration, with potential for further exploration in the research domain.

An improved supply of anthocyanin dye for creation of effective dye-sensitized solar cells grounded on natural dyes

Abstract In order to advance the power conversion efficiency of dye-sensitized solar cells, this article shows the selection of better sources of the sensitizer anthocyanin. The cells were created by combining liquid and solid electrolytes, adding natural dye, and employing a photo anode of aluminium-doped zinc oxide and a counter electrode of fluorine-doped tin oxide. Light harvesting efficiency, scanning electron microscopy, ultraviolet and infrared spectroscopy, and other methods were used to characterise the cells. From all the combinations made utilising different sources, the cell based on the D1 dye sample from Hibiscus sabdariffa L. (Manipur) had the best efficiency at 1.58 %. An effective DSSC was the end result of this strategy for identifying the optimal extraction source for anthocyanin natural dyes.

Emergent Optical Resonances in Atomically Phase-Patterned Semiconducting Monolayers of WS2.

Atomic-scale control of light-matter interactions represents the ultimate frontier for many applications in photonics and quantum technology. Two-dimensional semiconductors, including transition-metal dichalcogenides, are a promising platform to achieve such control due to the combination of an atomically thin geometry and convenient photophysical properties. Here, we demonstrate that a variety of durable polymorphic structures can be combined to generate additional optical resonances beyond the standard excitons. We theoretically predict and experimentally show that atomic-sized patches of the 1T phase within the 1H matrix form unique electronic bands that lead to the emergence of robust optical resonances with strong absorption, circularly polarized emission, and long radiative lifetimes. The atomic manipulation of two-dimensional semiconductors opens unexplored scenarios for light harvesting devices and exciton-based photonics.

Spectral modulation of B850 bacteriochlorophyll a in light-harvesting complex 2 from purple photosynthetic bacterium Thermochromatium tepidum by detergents and calcium ions

Spectral variations of light-harvesting (LH) proteins of purple photosynthetic bacteria provide insight into the molecular mechanisms underlying spectral tuning of circular bacteriochlorophyll (BChl) arrays, which play crucial roles in photoenergy conversion in these organisms. Here we investigate spectral changes of the Qy band of B850 BChl a in LH2 protein from purple sulfur bacterium Thermochromatium tepidum (tepidum-LH2) by detergents and Ca2+. The tepidum-LH2 solubilized with lauryl dimethylamine N-oxide and n-octyl-β-D-glucoside (LH2LDAO and LH2OG, respectively) exhibited blue-shift of the B850 Qy band with hypochromism compared with the tepidum-LH2 solubilized with n-dodecyl-β-D-maltoside (LH2DDM), resulting in the LH3-like spectral features. Resonance Raman spectroscopy indicated that this blue-shift was ascribable to the loss of hydrogen-bonding between the C3-acetyl group in B850 BChl a and the LH2 polypeptides. Ca2+ produced red-shift of the B850 Qy band in LH2LDAO by forming hydrogen-bond for the C3-acetyl group in B850 BChl a, probably due to a change in the microenvironmental structure around B850. Ca2+-induced red-shift was also observed in LH2OG although the B850 acetyl group is still free from hydrogen-bonding. Therefore, the Ca2+-induced B850 red-shift in LH2OG would originate from an electrostatic effect of Ca2+. The current results suggest that the B850 Qy band in tepidum-LH2 is primarily tuned by two mechanisms, namely the hydrogen-bonding of the B850 acetyl group and the electrostatic effect.

Alkyl effects on charge recombination in copper electrolyte-based dye-sensitized solar cells: Insights for targeted molecular design towards high performance

Two quinoxaline dyes utilized in copper-electrolyte-based dye-sensitized solar cells (Cu-DSSCs) are theoretically investigated to analyze the impact of alkyl chains on dye performance. The investigation shows that ZS4, known for its record efficiency of up to 13.2 %, exhibits higher electron coupling and fewer binding sites for dye-[Cu(tmby)2]2+ interaction compared to ZS5. Contrary to common belief, alkyl chains are found to not only provide shielding but also hinder the interaction between dye and [Cu(tmby)2]2+ by influencing the optimal conformation of dyes, thereby impeding the charge recombination process. It is crucial to consider the influence of alkyl chains on dye conformation when discussing the relationship between dye structure and performance, rather than oversimplifying it as often done traditionally. Building on these findings, eight dyes are strategically designed by adjusting the position of the alkyl chain to further decrease charge recombination compared to ZS4. Theoretical evaluation of these dyes reveals that changing the alkyl chain on the nitrogen atom from 2-ethylhexyl (ZS4) to 1-hexylheptyl (D3-2) not only reduces the charge recombination rate but also enhances light harvesting ability. Therefore, D3-2 shows potential as a candidate for experimental synthesis of high-performance Cu-DSSCs with improved efficiency.

Bulk photovoltaic effect in ferroelectric nematic liquid crystals.

The bulk photovoltaic (BPV) effect in ferroelectric liquid crystals is of increasing scientific interest owing to its great potential for light-energy conversion. The ferroelectric nematic phase exhibits a huge spontaneous polarization that can be aligned to a preferred direction. In this Letter, we investigate the tensorial properties of the BPV effect in the planarly aligned ferroelectric nematic phase of the liquid crystalline material RM734. A steady-state short-circuit photocurrent of ~160 pA and an open-circuit photovoltage of ~50 mV were observed in a cell with a thickness of 5.5 µm under the illumination of ultraviolet light without any bias voltage. Based on the photocurrent measurements in different electrode configurations, the non-zero elements of the BPV tensor were obtained. The BPV effect is attributed to the combination of the spontaneous polarization and the asymmetric distribution of photoinduced charge carriers. This study not only provides an understanding of the bulk PV mechanism in soft ferroelectrics but also promises a wide range of unprecedented, to the best of our knowledge, benefits for light harvesting to engineer marketable photovoltaic devices.

Microwave-assisted rapid synthesis of ZnO multipod-BiOBr heterojunction on recycled PET plastic waste for photocatalytic degradation of oily wastewater

Heterojunctions based on ZnO multipod and BiOBr were developed on the floating recycled polyethylene terephthalate (PET) and they were used to investigate the photocatalytic degradation of hexane in water emulsion. Characterizations of the synthesized ZnO-BiOBr-PET photocatalysts was performed using XRD, FESEM, EDX, BET/BJH, FTIR, UV-Vis DRS, PL, WCA, and CV analyses. The FESEM results demonstrated that ZnO multipods have been synthesized during the very short time of microwave heating that effectively hosted the highly dispersed BiOBr nanoplates, particularly in the 15 %ZnO-5 %BiOBr-80 %PET sample. The BET/BJH analysis revealed the low surface areas for the synthesized samples, however, the sample with the highest ZnO multipod loading (15 %ZnO-5 %BiOBr-80 %PET) exhibited slightly enhanced surface area due to the highly dispersed BiOBr over the ZnO multipods. The fabricated samples displayed hydrophobicity and liquid marble like behaviour due to the presence of PET, while the variations in the percentages of ZnO and BiOBr strongly influenced the water contact angle. The formation of heterojunction between ZnO multipod and BiOBr was confirmed which lead to a shift in the visible light region, increased the light harvesting, and also reduced the charge carrier recombination in the composite sample of 15 %ZnO-5 %BiOBr-80 %PET. The ZnO-BiOBr-PET photocatalysts were tested for the photocatalytic degradation of hexane in a water emulsion and results indicated that 15 %ZnO-5 %BiOBr-80 %PET could degrade 92.1 % of initial hexane, retaining its performance over four successive runs with only an 11.7 % decrease in activity. Scavenger tests revealed that, in addition to hydroxyl radicals, superoxide also played a significant role in the photocatalytic degradation of hexane. This obervations indicate the efficient capturing and utilizing of O2 by this LMP even in non-oxygenated conditions.