Photoinduced Degradation Research Articles

Cysteine assisted synthesis of Bi2S3/BiOBr nanocomposites for photocatalytic decomposition of rhodamine B

Novel Bi2S3/BiOBr nanocomposites (NCs) were prepared via L-Cysteine-assisted hydrothermal avenue as efficient photocatalysts to degrade rhodamine B (RhB). As a result, the obtained Bi2S3/BiOBr NCs exhibited the slice-like microstructure with the average diameters of ca. 100 nm. The elemental analysis of X-ray photoelectron spectroscopy indicates that the nanocomposites were combined by Bi2S3 and BiOBr. Then, the photo-induced degradation of RhB was performed with a Xenon lamp to simulate the sunlight ([Formula: see text] 400 nm) and the photo-decomposition rate was calculated. The following results showed that the Bi2S3/BiOBr NCs possessed excellent photocatalytice performance, which was better than that of other samples as control. Thus, this avenue provides a new reference for the facile synthesis of photocatalysts with low cost and high efficiency.

Radiation driven synthesis of MnSe nanoparticles with dual luminescence and magnetic characteristics and its role in photocatalytic reactions

Many biomedical applications can greatly benefit from the combination of photoluminescence and magnetic properties of non-toxic manganese-based nanomaterials and thus, it demands for synthesizing such materials in an aqueous environment. The present work reports aqueous synthesis of starch-capped manganese selenide (MnSe) nanoparticles (NPs) through a steady-state gamma irradiation route under ambient pressure and room temperature. As radiolysis is considered as the cleanest method among available chemical approaches, we preferred to employ this technique and endeavored to establish optimal conditions of such synthesis. The as-produced MnSe nanocrystals demonstrated strong photoluminescence with a quantum yield of ca. 32% and co-existence of paramagnetic with antiferromagnetic behavior. To look into possible light-induced reactions with aromatic molecules, the effectiveness of synthesized particles on photo-induced degradation of dyes of similar structure was investigated. The proposed strategy may pave the way for synthesizing magneto-fluorescent nanoparticles in aqueous medium, which may find immense scope in nano-photonics and nano-biotechnology including biological assays, labelling and imaging.

Radiometric characterization of daytime luminescent materials directly under the solar illumination

The materials efficiently emitting photoluminescence (PL) under solar irradiation could find broad applications in passive radiative cooling of buildings, urban heat mitigation, and solar energy harvesting. In this work, we discuss the limitations of common laboratory characterization of such materials (using tunable light sources or solar simulators) and propose a methodology for direct outdoor characterization of PL efficiency under full solar irradiation. A simple, portable radiometry setup with an integrating sphere is described, and its capability of rapid determination of the spectral distribution of the absorbed and emitted power, as well as the overall PL power efficiency and quantum yield, is demonstrated. By characterization of three materials developed for daytime radiative cooling applications, we reveal deviations of obtained parameters caused by the replacement of the real solar irradiation by that of solar simulators. The described method is suitable for studies of long-term stability, photo-induced degradation, or thermal effects.

Exceeding the theoretical limit of interfacial evaporation efficiency by using the carbon-based aerogel evaporator with cold evaporation surface

Solar-driven interfacial evaporation technology has shown significant potential in the field of water treatment. Heat loss is still inevitable during the SIE process, since the temperature at the evaporation interface surpasses both the ambient temperature and the temperature of the water below. In this study, we presented a study on an aerogel composed of reduced graphene oxide (rGO), multi-walled carbon nanotubes (MWCNTs) and polypyrrole (PPy). The self-aggregation effect of rGO was mitigated through π-π interactions with MWCNTs and PPy, resulting in the formation of a three-dimensional porous structure. This provided the aerogel with a large specific surface area for pollutant adsorption and ample pore volume for photo-induced degradation and photothermal water purification. Using infrared thermography, thermocouples and numerical simulation, it was demonstrated that introducing a cold evaporation surface resulted in thermal flow reversal. This process allowed the evaporator to extract energy from bulk water, thereby enhancing solar evaporation. Due to this gain, under one sun illumination, the aerogel reached an evaporation rate as high as 3.31 kg·m−2·h−1 and achieved an evaporation efficiency of 135.6 %. Simultaneously, the aerogel exhibited a photocatalytic efficiency of over 90 % for various organic pollutants (methylene blue trihydrate, trypan blue and tetracycline hydrochloride). Moreover, it also demonstrated excellent purification ability for combined wastewater, including high-salinity water, seawater and lubricant/water emulsions. Therefore, high-performance interfacial evaporators hold great promise for achieving sustainable wastewater purification and serve as a valuable reference for the development of new solar energy conversion systems.

Unified Crystal Phase Control with MACl for Inducing Single-Crystal-Like Perovskite Thin Films in High-Pressure Fusion Toward High Efficiency Perovskite Solar Cell Modules.

Perovskite solar cells, recognized for their high photovoltaic conversion efficiency (PCE), cost-effectiveness, and simple fabrication, face challenges in PCE improvement due to structural defects in polycrystalline films. This study introduces a novel fabrication method for perovskite films using methylammonium chloride (MACl) to align grain orientation uniformly, followed by a high-pressure process to merge these grains into a texture resembling single-crystal perovskite. Employing advanced visual fluorescence microscopy, charge dynamics in these films are analyzed, uncovering the significant impact of grain boundaries on photo-generated charge transport within perovskite crystals. A key discovery is that optimal charge transport efficiency and speed occur in grain centers when the grain size exceeds 10µm, challenging the traditional view that efficiency peaks when grain size surpasses film thickness to form a monolayer. Additionally, the presence of large-sized grains enhances ion activation energy, reducing ion migration under light and improving resistance to photo-induced degradation. In application, a perovskite solar cell module with large grains achieve a PCE of 22.45%, maintaining performance with no significant degradation under continuous white LED light at 100 mA cm-2 for over 1000h. This study offers a new approach to perovskite film fabrication and insights into optimizing perovskite solar cell modules.

Synergistic adsorption and UV degradation of perfluorooctanoic acid by amine-functionalized A-center sphalerite

Perfluorinated alkylated substances (PFAS), as a category of persistent organic pollutants, have garnered extensive concern due to their resilience against environmental degradation. Herein, we developed an amine-functionalized sphalerite (ZnS) with adjustable surface amine functional groups and Zn defects (ZnS-X%[N]) by in situ coprecipitation and simple hydrothermal method in the presence of cetyltrimethylammonium bromide (CTAB). This material demonstrated efficient PFAS adsorption and subsequent photo-induced degradation under UV irradiation. The characterization results by TEM, BET, FTIR, XPS and EPR revealed that CTAB primarily influences ZnS by modulating surface amine functionalities, zinc defect density, and enhancing its photoreductive capacity. Adsorption and kinetic degradation experiments further showed that a medium CTAB concentration in ZnS-40%[N] achieves highest PFAS adsorption capacity (Cmax: 0.201 mol kg-1), and the corresponding decomposition rate was the fastest (kde: 1.53; kdf: 1.19). This efficacy is attributed to the ZnS-40%[N]'s ideal adsorptive sites and surface shallow defects. Moreover, theoretical simulation also supports the above experimental inference. Overall, ZnS-X%[N] exhibits a synergistic effect on PFAS adsorption and degradation, showcasing its potential for environmental adaptability and practical application.

Photo-Induced Degradation of Priority Air Pollutants on TiO2-Based Coatings in Indoor and Outdoor Environments—A Mechanistic View of the Processes at the Air/Catalyst Interface

Photo-Induced Degradation of Priority Air Pollutants on TiO2-Based Coatings in Indoor and Outdoor Environments—A Mechanistic View of the Processes at the Air/Catalyst Interface

Surface Adsorption and Photoinduced Degradation: A Study of Spinel Ferrite Nanomaterials for Removal of a Model Organic Pollutant from Water.

Spinel oxide nanocrystals are attractive materials for photoinduced advanced oxidation processes that degrade organic pollutants in water due to their chemical stability and tunability, visible light absorption, and magnetic recoverability. However, a systematic understanding of the structural and chemical factors that control the reactivity of specific spinel oxide nanocrystal materials toward photoinduced degradation processes is lacking. This Perspective illustrates these knowledge gaps through an investigation into the impacts of surface chemistry and composition of spinel ferrite nanocrystals of formula MFe2O4 (M = Mg, Fe, Co, Ni, Cu, Zn) on their ability to remove a model organic pollutant (methyl orange (MO)) from water. We identify two mechanisms by which the nanocrystals remove MO from water: (i) surface adsorption and (ii) photoinduced degradation under visible light irradiation in the presence of hydrogen peroxide via the photo-Fenton reaction. Nanocrystals that do not contain any surface ligands are more effective at removing MO from water than nanocrystals that contain surface ligands, despite our observation that the ligand-less nanocrystals do not form stable colloidal dispersions in water, while ligand-coated nanocrystals are colloidally stable. For many of the spinel ferrite compositions studied here, the fraction of methyl orange removal via adsorption to the nanocrystal surface in the absence of photoexcitation is larger than the fraction removed under irradiation. Our data indicate that the composition-dependent surface charge of the nanocrystals controls the degree of surface adsorption of the charged MO molecule. Overall, these results demonstrate that careful consideration of the impacts of surface chemistry on the behavior of spinel ferrite nanocrystals is required to accurately assess and subsequently understand their activity toward the photoinduced degradation of organic molecules.

A Sacrificial Linker in Biodegradable Polyesters for Accelerated Photoinduced Degradation, Monitored by Continuous Atline SEC Analysis.

Polymeric materials that undergo photoinduced degradation have wide application in fields such as controlled release. Most methods for photoinduced degradation rely on the UV or near-UV region of the electromagnetic spectrum; however, use of the deeply penetrating and benign wavelengths of visible light offers a multitude of advantages. Here we report a lactone monomer for ring-opening copolymerizations to introduce a sacrificial linker into a polymer backbone which can be cleaved by reactive oxygen species which are produced by a photocatalyst under visible light irradiation. We find that copolymers of this material readily degrade under visible light. We followed polymer degradation using a continuous flow size exclusion chromatography system, the components of which are described herein.

Light-induced degradation of dimethylmercury in different natural waters

Photo-induced degradation of dimethylmercury (DMHg) is considered to be an important source for the generation of methylmercury (MMHg). However, studies on DMHg photodegradation are scarce, and it is even debatable about whether DMHg can be degraded in natural waters. Herein, we found that both DMHg and MMHg could be photodegraded in three natural waters collected from the Yellow River Delta, while in pure water only DMHg photodegradation occurred under visible light irradiation. The effects of different environmental factors on DMHg photodegradation were investigated, and the underlying mechanisms were elucidated by density functional theory calculations and a series of control experiments. Our findings revealed that the DMHg degradation rate was higher in the tidal creek water compared to Yellow River, Yan Lake, and purified water. NO3-, NO2-, and DOM could promote the photodegradation with DOM and NO3- showing particularly strong positive effects. Different light sources were employed, and UV light was found to be more effective in DMHg photodegradation. Moreover, MMHg was detected during the photodegradation of DMHg, confirming that the photochemical demethylation of DMHg is a source of MMHg in sunlit water. This work may provide a novel mechanistic insight into the DMHg photodegradation in natural waters and enrich the study of the global biogeochemical cycle of Hg.

Impact of photoinduced phase segregation in mixed-halide perovskite absorbers on their material and device stability

Mixed-halide perovskites enable bandgap engineering for tandem solar cell and light-emitting diode applications. However, photoinduced halide phase segregation introduces a compositional instability, that is, formation of I-rich and Br-rich phases, which compromises photovoltaic efficiency and stability. While optical and structural studies of the photoinduced phase segregation in mixed-halide perovskites have been reported, its impact on the material stability is missing. Here, a detailed compositional analysis of mixed-halide perovskite films using x-ray and ultraviolet photoelectron spectroscopy (UPS) was carried out to determine how their stability in various environments depends on the halide ratio. A series of perovskite thin films were fabricated with the composition CH3NH3Pb(IxBr1−x)3, where x = 0.00, 0.25, 0.50, 0.75, and 1.00, and analyzed under different conditions, such as exposure to light in ambient and in nitrogen atmosphere, as well as storage in the dark. From the spectroscopy results, complemented with structural and optical properties, it was found that the deletion of halide ions from the surface is facilitated in mixed-halide perovskites in comparison with pure halide perovskites. A higher stability was found for the mixed-halide perovskite containing less than 25% Br, and it decreases with increasing Br content. This study also established the effect of the Br/I ratio on the energy landscape of the materials. The UPS spectra reveal that photoinduced degradation results in a mismatch of the energy levels at the perovskite/transport layer interface, which may limit the collection of charge carriers. These findings correlate well with the photovoltaic device stability under similar degradation conditions.

UV irradiation behavior of Salix psammophila sand barriers in the process of desertification control.

Salix psammophila sand barriers degrade under sunlight exposure, resulting in diminished protective performance and shortened service life in desertification control. To address the unresolved issue of photoinduced damage and degradation in sand barriers, we conducted simulations to assess the accelerated damage effect of ultraviolet (UV) rays during solar exposure of S. psammophila sand barriers. Our analysis focused on elucidating the mechanism of UV irradiation in sand barriers by examining the structural and material property changes that occur during the degradation process. The results indicated the following: (1) The discoloration of sand barriers resulting from UV irradiation was primarily ascribed to the modification in lignin content. (2) The morphology and protective performance of S. psammophila sand barriers underwent significant changes following exposure to UV irradiation. The 96-day and 144-day time points of UV exposure are crucial for evaluating the extent of UV degradation in sand barriers. After 192 days of UV irradiation, there was a decrease in mass loss percentage by 3.62%, modulus of elasticity by 8.63%, and modulus of rupture by 6.74%. (3) The lignin, hemicellulose, and cellulose content decreased by 23.12%, 14.30%, and 6.96%, respectively. The impact of UV irradiation on the polysaccharide (cellulose and hemicellulose) in S. psammophila sand barriers was relatively minimal. (4) The carbon binding form in S. psammophila sand barriers underwent a transformation, characterized by a significant decrease in C1 content and an increase in C2 and C3 content. This resulted in a gradual enhancement of the oxidation state and binding energy of carbon. Therefore, to prolong the utilization lifespan of S. psammophila sand barriers, it is essential to address the UV irradiation behavior from the perspective of inhibiting lignin reactions.

Metal-free upcycling of plastic waste: photo-induced oxidative degradation of polystyrene in air

A photooxidation method was reported to facilitate the efficient degradation of polystyrene (PS) in air using porphyrin-based porous organic polymers (PPOPs). The method is mild and effective in promoting the degradation of different PS derivatives.

Strategies for Sustainable Fuel Production Via Photoelectrochemical Synthesis

Developing sustainable energy is highly imperative for humankind owing to the drastic rise in world population and the proportional rise in energy demand at the expense of energy consumption. Various efforts have been made to explore, generate, store, and utilize renewable energy to replace fossil fuels. Among them, solar energy is considered an alternative to fossil fuels because it is inexhaustible, clean, cost-effective, and versatile. Interestingly, this prime source provides massive energy that is high enough (1.9 × 108 TWh/yr) to counterattack global energy consumption (1.3 × 105 TWh/yr).Photoelectrochemistry has been considered a promising route to harness this incredible energy by producing sustainable energy fuels and carriers such as hydrogen, hydrocarbon, and ammonia. PEC systems have the great advantages of simple process steps and very low environmental burdens. However, this technology must overcome many challenges regarding commercial applications, particularly in fabricating electrode materials for PEC water splitting.One of the most important challenges to overcome this problem is discovering efficient catalysts for implementing photoelectrochemical (PEC) fuel production. A critical requirement for outstanding catalysts is an ability to boost the kinetics of a chemical reaction and durability against electrochemical and photo-induced degradation. Moreover, the charge-separation and transfer mechanism are the two paramount properties to consider while designing photoelectrodes. Briefly, the semiconductor materials to be used in PEC water splitting must possess a conduction band potential more negative than the reduction edge of hydrogen and a valence band potential positive to actuate water oxidation. In practice, the photocurrent density and solar-to-hydrogen (STH) efficiency of the n-type semiconductors are far behind the theoretical values.To address this critical and long-standing technical barrier, I have focused on an intense search for efficient, durable, and inexpensive alternative catalysts with moderate band gap, efficient charge excitation-separation property, and high solar energy conversion efficiency for photoelectrochemical systems of water splitting, hydrocarbon conversion, and ammonia production. Keywords : Photoelectrochemistry, Sustainable Energy, Water Splitting, Ammonia synthesis, Urea synthesis, Hydrocarbon

Evaluation of the photocatalytic degradation mechanism of methylene blue using nascent and Ag+ ions-modified TiO2.

In photocatalytic removal of organic pollutants, adsorption and degradation are two important processes that take place. Various instrumental techniques and trapping experiments have been used to identify the reactive species and the mechanism of photodegradation. The present work focuses on investigating the mechanism of photo-induced degradation from the comparative characterization of fresh and used samples, isotherm models, competitive adsorption, and desorption studies of pure and Ag+-modified TiO2 NPs. The comparative characterizations of fresh and used NPs were carried out with FT-IR, EDX, and XRF analyses after methylene blue (MB) degradation. The Ag+ doped TiO2 used in this study was fabricated using simple impregnation technique. The prepared NPs were characterized using techniques including XPS, XRD, SEM/EDX, XRF, UV-DRS, and pH point-zero charge analyses (pHPZC). The Ag+-modified TiO2 NPs showed improved efficiency compared to pure TiO2 NPs using normal compact fluorescent light (CFL). The Langmuir and Freundlich isotherm models were applied to test the adsorption behavior on the surface photocatalysts. The investigational data finest fitted to the Langmuir isotherms model compared to Freundlich model, suggesting the homogeneous monolayer adsorption followed by degradations. The competitive removal of MB in the presence of a photo-generated electrons trapper (Cd2+) was enhanced almost 3-folds (115mg/L) compared to the removal from a single MB solution (40mg/L). The characterization of the used samples as well as adsorption in the dark and negligible desorption of used samples support the involvement of the proposed photo-induced degradation mechanism.

Nano-island-like heterojunction of nitrogen-doped carbon quantum dots anchoring on titanium oxide nano sheets@Cu2O for enhancing visible light-driving photocatalytic degradation of methyl orange

Cu2O and TiO2 are promising for photocatalysis owing to their lower cost and excellent performance. Unfortunately, the efficiency of light utilization by Cu2O and TiO2 is still low. Herein, the nano-island-like heterojunction of nitrogen-doped carbon quantum dots anchoring on titanium oxide nano sheets@Cu2O (NCQDs/TNSs@Cu2O) was synthesized through the hydrothermal and chemical precipitation process and its photocatalytic performance was systematically characterized. Benefiting from the unique heterojunction, NCQDs/TNSs@Cu2O exhibited a superior photocatalytic performance. High-resolution transmission electron microscopy showed that NCQDs/TNSs nanoclusters were decorated on Cu2O nanoparticle surface and formed heterojunctions. The UV–Vis-DRS spectra indicated that NCQDs/TNSs@Cu2O exhibited the strong adsorption peaks between 400 and 650 nm. Under simulated sunlight irradiation, NCQDs/TNSs@Cu2O exhibited excellent photocatalytic degradation performance on methyl orange. For example, the degradation was completed within 20 min and the photo-degradation capacity of NCQDs/TNSs@Cu2O remained 90.1 % after four recycling cycles. Furthermore, the potential mechanism for the photo-induced degradation was proposed based on the active substances identified through the electron spin resonance. Conclusively, this study provides a novel perspective on the role of NCQDs and prepares the way for the design of the biomass-based photocatalyst.

Photoacid Generators for Biomedical Applications.

Photoacid generators (PAGs) are compounds capable of producing hydrogen protons (H+ ) upon irradiation, including irreversible and reversible PAGs, which have been widely studied in photoinduced polymerization and degradation for a long time. In recent years, the applications of PAGs in the biomedical field have attracted more attention due to their promising clinical value. So, an increasing number of novel PAGs have been reported. In this review, the recent progresses of PAGs for biomedical applications is systematically summarized, including tumor treatment, antibacterial treatment, regulation of protein folding and unfolding, control of drug release and so on. Furthermore, a concept of water-dependent reversible photoacid (W-RPA) and its antitumor effect are highlighted. Eventually, the challenges of PAGs for clinical applications are discussed.

Green Synthesis of TiO2 Using Impatiens rothii Hook.f. Leaf Extract for Efficient Removal of Methylene Blue Dye.

In this work, TiO2 nanoparticles (NPs) were effectively synthesized by a green method using the Impatiens rothii Hook.f. leaf (IL) extract as a capping and reducing agent. The as-synthesized TiO2 NPs were characterized by different characterization methods such as the Brunauer-Emmett-Teller (BET) analysis, high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), diffused reflectance spectroscopy (DRS), and X-ray diffraction (XRD) and Raman spectroscopy. The specific surface area from BET analysis was found to be 65 m2/g. The average crystallite size from XRD analysis and average particle size from SEM analysis were found to be ∼11 and ∼25 nm, respectively. The Raman spectroscopy and XRD results showed that the biosynthesized (IL-TiO2) nanoparticles were purely anatase phase. XPS analysis illustrated the formation of Titania with an oxidation state of +4. The DRS study showcased that a blue-shifted intense absorption peak of IL-TiO2 (3.39 eV) compared to the bulk material reported in the literature (3.2 eV). HRTEM micrograph showed the presence of grain boundary with d spacings of 0.352, 0.245, and 0.190, which correspond to the lattice planes of (101), (004), and (200), respectively. From the EDX analysis, the weight percents of titanium and oxygen were found to be 54.33 and 45.67%, respectively. The photoinduced degradation of methylene blue (MB) dye was investigated in the presence of biosynthesized IL-TiO2 NPs photocatalyst. The effect of parameters like catalyst dosage (30 mg/L), initial concentration of MB (15 ppm), pH (10.5), and contact time (100 min) on the removal efficiency was optimized. The maximum photodegradation efficiency under the optimized conditions was found to be 98%.

Univariate and multivariate kinetic and structural analysis of photoinduced tetracycline degradation

Tetracycline antibiotics found in waters worldwide pose a tremendous ecological and human health hazard due to bacterial resistances. Various processes are currently investigated to eliminate such anthropogenic micropollutants, among them advanced oxidation processes, where hydroxyl radicals cause disintegration of many organic substances. For mechanistic understanding and optimization for potential in-field use, kinetic descriptions and chemical reaction knowledge are important. Structural identification, quantitation and kinetic description of the substances are investigated via a univariate method, i.e. high-performance liquid-chromatography coupled with mass spectrometry and curve-fitting, and a multivariate method, i.e. absorption spectroscopy and curve resolution-alternating least squares fitting. The latter represented a fast, non-laborious analytical method. The univariate approach revealed four known and two new transformation products. First-order kinetics with follow-up reactions were observed. The univariate method yielded rate constants of about 0.33 min−1 for the degradation of both tetracyclines and distinct rate constants for transformation products, while rate constants of about 0.22 and 0.27 min−1 and an overall rate constant for non-identified transformation products were obtained from multivariate analysis due to the insufficient discriminatory power. Structural characterization, fast and easy kinetic parameter determination of photoinduced degradation may contribute to optimize advanced oxidation processes for the removal of antibiotics from waste water.

On the photoinduced degradation of tamsulosin: The simpler the better

In this work, we present a comprehensive investigation of the decomposition of tamsulosin. Experiments were performed in an aqueous solution through photolysis with a 254 nm light source. In general, tamsulosin degradation was observed (presenting a rate of 35.4%, in 180 min), demonstrating that direct photoinduced decomposition is efficient. The simpler uncatalyzed process worked while previous experiments using solid catalysts showed negligible degradation. The kinetic constant of the photolysis process (17.6 ×10−3 min−1) was determined, considering first order kinetics, by fitting plots of ln([Tam]t −[Tam]∞)/ln([Tam]0 −[Tam]∞) versus irradiation time, where [Tam]t is the concentration of tamsulosin at time t, and [Tam]∞ is the limiting concentration of the reacting system. In addition, physical insights regarding tamsulosin photoexcitation and photolysis were obtained through quantum chemistry computations. Density functional theory (DFT) was used to investigate the ground state while its time-dependent formalism (TD-DFT) was used for determining vertical excitation energies and generalized oscillator strengths (GOSs). All the computations were undertaken at the CAM-B3LYP/6-311++G(d,p) level of theory, in water. Regarding the excited states, all five lowest-lying states were determined to have non-zero GOSs, with S3 (found at 5.73 eV (∼216 nm) at the TD-DFT/CAM-B3LYP/6–311++G(d,p) level of theory) presenting the highest GOS (0.1157) among all. Hence, these accessible states may be assigned as those responsible for the photoinduced degradation observed experimentally. Moreover, the computational results suggest tamsulosin undergoes photodecomposition through excited state chemical reaction rather than via a direct photolysis path.