Photoconversion Efficiency Research Articles

Harnessing the Potential of Morphologically Tailored ZnSn(OH)6 Nanograss Photoanode for Solar‐Driven Water Splitting

AbstractHydrothermal growth of ZnSn(OH)6 nanograss on ZnO‐coated FTO substrates is demonstrated. Effect of surfactants addition (polyvinylpyrrolidone and polyethylene glycol), precursor concentration, and reaction temperature on surface morphology of ZnSn(OH)6 nanograss are investigated. Addition of surfactant in precursor solution results in growth of approximately 20–30 nm thick nanograss morphology with varying orientation. The nanograss grow longer by increasing the concentration of precursors solution. The grown ZnSn(OH)6, exhibits XRD peaks corresponding to cubic phase ZnSn(OH)6. Optical bandgap of the grown nanograss are calculated in the range from ∼3.0 to 3.5 eV. The nanograss photoanode grown with PEG surfactant (at 200 °C) has shown the highest photocurrent of 2.2 mA/cm2 at RHE 1.23VRHE and photoconversion efficiency of 1.4% at 0.46 VRHE. The longer nanograss has shown lower charge transfer resistance and higher charge carrier concentration, which is favorable for enhancing the PEC performance.

Layer-by-Layer Deposition of Hollow TiO2 Spheres with Enhanced Photoelectric Conversion Efficiency for Dye-Sensitized Solar Cell Applications

Fabricating photoanodes with a strong light-scattering effect can improve the photoconversion efficiency of dye-sensitized solar cells (DSSCs). In this work, a facile microwave hydrothermal process was developed to prepare Au@TiO2 core–shell nanostructures, and then the Au core was removed by etching, resulting in hollow TiO2. Morphological characterizations such as field emission scanning and transmission electron microscopy measurements have been used for the successful formation of core–shell and hollow TiO2 nanostructures. Next, we attempted to deposit the different-sized hollow TiO2-based microspheres simultaneously on the surface of small-sized TiO2 nanoparticles-based compact film as light-scattering layers via electrophoretic deposition. The deposited hollow TiO2 microspheres constitute bi- and tri-layers that not only improve the light-harvesting properties but also speed up the photogenerated charge transfer. Compared to commercial TiO2 compact film (4.75%), the resulting bi-layer and tri-layered films-based DSSCs displayed power conversion efficiencies of 6.33% and 8.08%, respectively. It is revealed that the deposited bi- and tri-layered films can enhance the light absorption ability via multiple photon reflection. This work validates a novel and controllable strategy to develop light-scattering layers with increased light-harvesting properties for highly efficient dye-sensitized solar cells.

A comparative numerical simulation study of CIGS solar cells with distinct back surface field layers for enhanced performance

The objective of this study is to explore the impact of various back surface field (BSF) layers including copper aluminium oxide (CuAlO2), Copper Antimony Sulphide (CuSbS2), Formamidinium tin triiodide (FASnI3), poly(3-hexylthiophene) P3HT to boost the output of conventional baseline CIGS solar cells structured. The device performance increases because of the minimized surface recombination velocity through heavily doped BSF layers, which increases the electric field at the rear contact. Among all proposed BSF layers CuAlO2 gives the best photoconversion efficiency (η) of 24.61% followed by fill factor (FF) of 83.11 %, short circuit current density (JSC) of 35.87 mA/cm2, and open circuit voltage (VOC) of 0.82 V with quantum efficiency (QE) of ∼92 % for the whole visible range with the onset happening at ∼ 560 nm, thanks to the enhancement of carrier collection when BSF layer is incorporated. The novelty in this work is that for the first time with the CuAlO2 BSF layer, 24.61% efficiency is reported at 1 μm CIGS layer thickness. We also examined how different BSFs affect the PV performance of the devices. The effect of temperature, the doping concentration of the BSFs, varying gallium proportion, JV & QE analysis, band diagram, and radiative recombination coefficient are varied to observe their impact on the PV parameters. This research introduces novel CIGS/CdS heterojunction configurations using various BSF layers to enhance efficiency, supporting the advancement of ultrathin, flexible, and tandem solar cell applications.

Cr3+-doped Na2CaSn2Ge3O12 garnet showing broadband near-infrared emission at 820 nm with zero thermal quenching and near-unity quantum yield

The continually advancing near-infrared (NIR) phosphor-converted light-emitting diode (pc-LED) hold pivotal significance in optical imaging and NIR spectroscopy. Cr3+-doped garnet broadband NIR phosphors have attracted considerable attention owing to their high optical performance enabled by the rigid structure. Nonetheless, the emission wavelength is severely restricted, and longer wavelength emissions usually result in inferior quantum efficiency and poor luminescence stability. In this work, the concurrent reconstruction of dodecahedral and octahedral sites by introducing [Na+-Sn4+]C unit in the framework of Na2CaSn2Ge3O12 garnet contributes to the Cr3+ broadband NIR emission spanning 700–1200 nm, with a peak at 820 nm. Utilizing a charge compensation strategy via Ta5+ codoping largely boosts the internal quantum efficiency (IQE) of Na2CaSn2Ge3O12:Cr3+ from 93.06 % up to 95.04 %. Trap-mediated energy compensation is proposed to achieve a record-breaking zero-thermal-quenching behavior (99.39 %@423 K) of Cr3+-doped garnet with such a longer wavelength emission. The encapsulated prototype broadband NIR pc–LED gives rise to an overwhelming NIR output power of 590.9 mW@1300 mA and a photoconversion efficiency (PCE) of 32.62 % at 30 mA, rendering exceptional performance in night vision, detection, and NIR imaging applications.

Optimization of the solar cell based on cadmium telluride by adding the CdSeTe absorbing layer (heterostructure simulation)

Cadmium telluride solar cells are among the most common devices for photovoltaic applications. However, the energy conversion efficiency of these elements remains insufficiently high. Using the SCAPS programming environment, research and optimization of a classical thin-film solar cell based on CdTe were carried out. The structure of this element consisted of ITO as a transparent conductive contact, a cadmium sulfide (CdS) layer, and a cadmium telluride (CdTe) absorber layer with a metal contact. To optimize this structure in terms of power conversion efficiency, the influence of the thickness and concentration of acceptor impurities in the CdTe absorbing layer, as well as the influence of the thickness and concentration of donor impurities in the CdS buffer layer, were considered. It was established that the optimal thicknesses for the CdS buffer layer and absorption CdTe layers are 50 nm and 3000 nm, respectively. An additional CdSeTe layer between the CdS and CdTe layers has been proposed as one of the optimization options to improve the device efficiency. The main photovoltaic parameters of such a solar cell were analyzed depending on the thickness of the CdSeTe layer and its selenium content. It has been demonstrated that adding CdSeTe solid solution to the 1500 nm thick CdTe absorber layer increases the efficiency of the solar cell by 6.84 %. The main photovoltaic characteristics of CdS/CdTe and CdS/CdSeTe/CdTe solar cells were compared. The results showed that the simulated CdS/CdSeTe/CdTe structure provides better photoconversion efficiency in the AM1.5G light spectrum compared to the classical CdS/CdTe structure. Such elements can be used to form highly efficient solar panels

Exploring the potential of CdSe nanostructured thin films for energy conversion and environmental remediation

Abstract The rapid thermal evaporation method was employed to prepare cadmium selenide (CdSe) nanostructured thin films with varying thicknesses on glass and FTO substrates. The films were characterized for their structural, optical, and electrochemical properties. Scanning electron microscope (SEM) analysis revealed inhomogeneous surfaces with particle sizes ranging from 18 to 46 nm. The photocatalytic performance of the CdSe films was evaluated by the degradation of methylene blue (MB) dye under visible light, with varying pH values, achieving a degradation efficiency of 100 % at pH 10 after 180 minutes. Photocurrent density measurements demonstrated the films' ability to sense visible light. We performed a cyclic voltammetry (CV) measurement and analyzed the CV curves of the CdSe nanostructured thin film electrodes. It clearly shows that the CV curves had a rectangular shape, which suggests that EDLC behavior was present and non-faradaic capacitance was the main type. The photoconversion efficiency measured is 1.4858 at a bias voltage of 0.66 V under illuminated conditions. Nonlinear optical properties were conducted for CdSe nanostructured thin films.

Green carbon nanospheres for integrated photo-supercapacitors device with improved efficiency

Achieving a low-cost, high-yield, and environmentally acceptable synthesis of graphene is a significant problem in nanomaterials research. Hence, carbon nanospheres are receiving an increased attention. We have developed a unique and cost-effective method of producing carbon nanospheres from carbon soot. Carbon nanospheres were created using castor oil and virgin green leaf (Anisomeles Malabarica) and then thoroughly examined. When applied to dye-sensitised solar cells and the integrated photo-supercapacitor, the produced soot exhibited the same behavior as reduced graphene oxide. Photoconversion efficiency was 8.47 % in the dye-sensitised solar cells application and in the symmetric supercapacitor device application, it exhibited 11.83 mWh/cm2 of energy density and 0.3 mW/cm2 of power density which illuminated an LED bulb up to 60 s. The capacitive retention of 85.2 % was achieved after 3000 cycles. Finally, the integrated photo-supercapacitor performed about 3.3 % of the overall efficiency and 38 % of the storage efficiency.

A hybrid MAPbI3/PEDOT-ZrO2 perovskedot composite for enhanced stability and charge transport in photo-batteries

Designing flexible photo-batteries that are capable of charged directly by light is critical for improving off-grid power options. This paper presents a unique photo-battery design that uses a MAPbI3/PEDOT as the effective light-harvesting and hole-transporting layer, and zirconium oxide (ZrO2) as the channel for electrons and hole-blocking layer. The MAPbI3 perovskite material absorbs sunlight and develops charge carriers, while PEDOT helps transport holes to the anode, improving charge separation and minimizing recombination losses. ZrO2, with its strong electron mobility and great chemical stability, provides fast transport of electrons to the cathode. It also efficiently blocks holes, increasing overall charge transfer dynamics. This improved design improves photo-conversion efficiency by up to 0.51 % and has a high capacity retention rate of around 96 % after 500 cycles. This improved MAPbI3/PEDOT/ZrO2 photo-battery could decrease light charging time by three times, enabling adaptable, light-rechargeable batteries more practical for real-world applications.

Comparative Analysis of Anodized TiO2 Nanotubes and Hydrothermally Synthesized TiO2 Nanotubes: Morphological, Structural, and Photoelectrochemical Properties.

This study presents a comparative analysis of anodization and hydrothermal techniques for synthesizing TiO2 nanotubes directly on titanium foil. It emphasizes its advantages as a substrate due to its superior conductivity and efficient charge transfer. Optimized synthesis conditions enable a thorough evaluation of the resulting nanotubes' morphology, structure, and optical properties, ultimately assessing their photoelectrochemical and photocatalytic performances. Scanning electron microscopy (SEM) reveals differences in tube diameter and organization. An X-ray diffraction (XRD) analysis shows a dominant anatase (101) crystal phase in both methods, with the hydrothermally synthesized nanotubes exhibiting a biphase structure after annealing at 500 °C. UV-Vis and photoluminescence analyses indicate slight variations in band gaps (around 0.02 eV) and recombination rates. The anodized TiO2 nanotubes, exhibiting superior hydrophilicity and order, demonstrate significantly enhanced photocatalytic degradation of a model pollutant, amido black (80 vs. 78%), and achieve a 0.1% higher photoconversion efficiency compared to the hydrothermally synthesized tubes. This study underscores the potential advantages of the anodization method for photocatalytic applications, particularly by demonstrating the efficacy of direct TiO2 nanotube growth on titanium foil for efficient photocatalysis.

Aluminum-Doped Indium Oxide Electron Transport Layer Grown by Atomic Layer Deposition: Highly Efficient and Damage-Resistant Interconnection Solution for All-Perovskite Tandem Solar Cells with 25.46% Efficiency.

In fabricating high-efficiency all-perovskite tandem solar cells (APTSCs) with a p-i-n configuration, the electron transport layer (ETL) plays a critical role in facilitating the transport of photogenerated electrons from the front cell to the recombination layer and protecting the front cell from damage during rear cell fabrication. This study introduces aluminum-doped In2O3 (AIO) films grown by atomic layer deposition (ALD) as a promising ETL for high-efficiency APTSCs. ALD-grown AIO films with an optimized Al concentration exhibit superior charge transport characteristics, excellent transparency, and damage-resistant barrier properties against solution infiltration compared with conventional SnO2 ETLs and undoped ALD In2O3. Using an ALD SnO2/3 at.% AIO bilayer as the electron transport layer, an efficiency of 18.33% is achieved from single-junction wide bandgap perovskite solar cells. Furthermore, the use of ALD SnO2/3 at.% AIO ETL enables the reliable fabrication of APTSCs with negligible solution damage to the front cell and minimized power loss. Consequently, APTSC employing the ALD AIO-based ETL exhibit an excellent photoconversion efficiency of 25.46%, outperforming APTSCs with the ALD SnO2 ETL.

Anodic Synthesis of Highly Ordered TiO2 Nanotube Arrays: Role of Electrolyte Composition on the Structural, Morphological, Optical, and Photo-electrochemical Properties

The fluoride species present in two different anodizing electrolytes were used to produce TiO2 nanotube arrays (TiO2 NTAs) by simultaneous anodic reaction and chemical dissolution. In this investigation, two different electrolytes were used for the preparation; [Eth-TiO2 NAs: 95 ml ethylene glycol+0.5% NH4F+5 ml DI water] and [Gly-TiO2 NAs: 75 ml glycerine+0.5% NH4F+25 ml DI water]. The effects of the prepared electrolytes used in the synthesis of TiO2 nanotube arrays on structural element composition, morphology, and optical properties are the focus of this study and are characterized by X-ray diffraction (XRD), scanning electron microscopy field emission (FE-SEM), energy-dispersive X-ray spectroscopy (EDX) and UV-vis diffusion reflection spectroscopy (DRS), respectively. The photoelectrochemical properties of TiO2 NTAs prepared in different electrolytes were investigated. The photoelectrochemical performance of TiO2 NTAs in Na2SO3 (0.1 M) and Na2S (0.1) was examined under the light of 100 mW/cm2 from a xenon lamp. Comparing the photoelectrochemical (PEC) results of both electrolytes, we find that Eth-TiO2 NTAs contribute a wide surface area resulting in an enhanced PEC response. TiO2 NTs, which were prepared with Eth-TiO2 NTAs, exhibited the highest photocurrent density, 0.326 mA cm–2, and photoconversion efficiency (0.22%).

Efficient and Scalable Radiative Cooling for Photovoltaics Using Solution‐Processable and Solar‐Transparent Mesoporous Nanoparticles

AbstractContinuous heat generation in perovskite solar cells (PSCs), caused by solar radiation, poses a significant challenge to their lifespan. Existing active cooling methods require extra energy input and might not be effective at high temperatures. Most reported passive radiative cooling materials either lack solar transparency or require complex fabrication processes. Here, mesoporous silica nanoparticles are designed, synthesized, and assembled into multilayered stacks with a graded refractive index (GRI) by spray coating them on top of PSCs made from methylammonium lead iodide (MAPbI3) over a large scale (15.6 × 15.6 cm2). This coating offers both high transparency in the visible wavelength and high emissivity in the mid‐infrared region, leading to an average temperature reduction of 6.65 ± 1.48 °C in GRI‐coated MAPbI3 PSCs under outdoor conditions compared to non‐coated references. After 50 d, the GRI‐coated PSCs maintain 80.9 ± 8.7% of their initial photoconversion efficiency, in contrast to 6.1 ± 5.9% for the noncoated ones. The calculated cooling power of the GRI‐coated PSCs is 28.9% higher than that of the reference cells.

MIL-125-PDI/ZnIn2S4 Inorganic-Organic S-Scheme Heterojunction With Hierarchical Hollow Nanodisc Structure for Efficient Hydrogen Evolution from Antibiotic Wastewater Remediation.

Efficient photocatalytic production of H2 from wastewater is expected to address environmental pollution and energy crises effectively. However, the rapid recombination of photoinduced carriers results in low photoconversion efficiency. At present, inorganic-organic S-scheme heterojunction have become a prominent and promising technology. In this study, an organic ligand modified MIL-125-PDI/ZnIn2S4 (ZIS) inorganic-organic S-scheme heterojunction catalyst is designed. ZIS nanosheets are grown on the disc-shaped MIL-125-PDI surface to form a distinctive hollow nanodiscs with hierarchical structure, giving the material an abundance of surface active sites, an optimized electronic structure, and a spatially separated redox surface. Consequently, the optimal 100MIL-125-PDI250/ZIS exhibited high photocatalytic HER of 508.99 µmol g-1 h-1 in Tetracycline hydrochloride (TC-HCl) solution. Meanwhile, the catalyst achieved complete TC-HCl removal and mineralization rate of 66.62% in 4h. Experimental and theoretical calculations corroborate that the staggered band alignment and work function difference between MIL-125-PDI and ZIS induce the formation of a built-in electric field, thus regulating the charge transfer routes and consequently enhancing charge separation efficiency. The possible photocatalytic mechanism is analyzed using liquid chromatography-mass spectrometry (LC-MS), and the toxicities of the degradation products are also evaluated. This work presents a green dual-function strategy for H2 production and antibiotic wastewater recycling.

Simulation of the functionality of ZnO, TiO2 and Ta2O5, and MoO2 carrier selective contacts of GaAs0.99Bi0.01 nanowire-based solar cells

Abstract Photovoltaic performance of perpendicularly aligned GaAs0.99Bi0.01/CSC/ITO core-shell nanowire solar cell is thoroughly investigated in this simulation based theoretical study for both electron selective contact (ESC) and hole selective contact (HSC) as carrier selective contact (CSC) shell around GaAs0.99Bi0.01 core nanowire. The overall performance has been compared with radial PiN doped GaAs0.99Bi0.01 NWSC to mark the improvement caused by carrier selectivity. ZnO, TiO2, and Ta2O5 materials have been chosen as ESC material and MoO2 is chosen as HSC material in order to carry out this comparative study. We have thoroughly performed geometry optimization test over a wide range of periods in order to select the optimized ITO (Indium Tin Oxide) thickness for obtaining maximum photo current generation. The maximum short circuit photo current density (Jsc) of 38.76 mA/cm2 is obtained with ZnO coated nanowire solar cell (NWSC) for a pitch (P) of 400 nm and ITO shell thickness of 90 nm. For this optimized geometry, TiO2, Ta2O5 and MoO2 coated structures offered Jsc of 35.82 mA/cm2, 35.69 mA/cm2, and 35.27 mA/cm2 respectively and the uncoated NW generated Jsc of 31.15 mA/cm2. The planar structure without coating exhibits a Jsc of 24.86 mA/cm2, which is significantly lower than the nanostructured solar cells. Finally Lumerical 3D charge transport simulator is used to perform the electrical stimulation of ZnO coated structure, which offers maximum ideal Jsc. A detailed electrical performance analysis of GaAs0.99Bi0.01/CSC/ITO unit nanowire solar cell for ZnO, TiO2, Ta2O5 as ESC and MoO2 as HSC have also been covered in this article which reveals that ZnO as ESC possesses promising potential for designing highly efficient solar cells as it offers a photo conversion efficiency(PCE) of the order of 25% and open circuit voltage (Voc) even for very less minority carrier lifetime (Ʈn) 0.1 ns of GaAs0.99Bi0.01 and 1ps Ʈn of ZnO.

Enhanced visible light-driven photocathodic protection performance of CuBi2O4 modified TiO2 nanotube array S-type nano-heterojunction photoanodes for 316 stainless steel

CuBi2O4 (CBO) nanoparticle (NP)-sensitized TiO2 nanotube (NT) photoanodes have been prepared and optimized for high visible light utilization and photoconversion efficiency. The introduction of CBO significantly improved the charge generation/separation efficiency of the prepared photoanodes. The CBO-sensitized TiO2 NTs obtained with an electrodeposition time of 6 min had the best photocathodic protection (PCP) performance, and the photogeneration potential of CuBi2O4/TiO2 (CBOT) composites coupled to 316 stainless steel (SS) decreased by an additional 460 mV compared to that of TiO2. The CBO NPs were uniformly distributed on the TiO2 NTs to form tight interfacial bonds. Moreover, the one-dimensional TiO2 NTs act as direct electron channels, ensuring the fast collection of carriers generated by the system. The electronic lifetime of the 6CBOT composite is approximately 30 times that of the pure TiO2 material. In addition, the formation of S-type nano-heterojunction inside the CBOT not only promotes charge transfer in the system, but also retains a strong redox capacity compared to that of single TiO2 NTs. This work offers novel ideas in designing photoanode with efficient PCP property.

Flower-like SnS2/rGO composites with efficient iodide-triiodide redox performance for counter electrodes in Pt-free dye-sensitized solar cells

The work function (WF) of the counter electrode (CE) predominantly determines the device performance of dye sensitized solar cells (DSSCs) as it controls the electron transfer rate for dye regeneration. Hence in this work, tin disulphide/reduced graphene oxide (SnS2/rGO) composites were synthesized with different wt.% of rGO (3, 5, 7, 10 %) and investigated their performance in DSSCs applications. At the outset, the formation of pristine SnS2 and SnS2/rGO composites were confirmed through X-ray diffraction and Raman spectral analysis. The morphological imaging revealed the micro flower-like structure of SnS2 with cross-sectional width of 5 ± 0.2 μm, and petal thickness ranges from 30.7 nm to 46.4 nm. The binding energy spectra confirms the 4+ oxidation state of Sn in both SnS2 and 7 wt% SnS2/rGO, suggesting that the rGO does not alter the chemical states of SnS2. Further, the peak-to-peak separation values obtained from Cylic-Voltammetry analysis were found to be 0.37 and 0.57 V for S7 and Pt CE respectively, indicating the rapid electrolyte reduction of 7 wt% SnS2/rGO. Finally, a photo conversion efficiency (PCE) of 7.3 % has been achieved with 7 wt% SnS2/rGO CE which is greater than that of the PCE with Pt CE (6.5 %) and also higher than that of pristine SnS2 with 4.7 %. The improved PCE is attributed to the reduced WF of the 7 wt% SnS2/rGO composite as measured from the Kelvin probe force microscopy analysis, enabling the rapid redox reaction towards triiodide reduction.

Transformative and sustainable approach to waste plastic mixture valorization

The development of innovative methods for waste plastic valorization can benefit the environment and economy. In this study, the full spectrum of products (gas, oil, and solid products) resulting from the pyrolysis–reforming of a plastic mixture functioned as precursors of value-added products: 1) ethylene–propylene copolymers, 2) polyacrylonitrile (PAN)-based carbon nanofibers (CNFs), and 3) carbon quantum dots (CQDs). The CNFs were subsequently applied as supercapacitor electrodes, whereasthe CQDs acted as co-sensitizers for the primary sensitizer, N3, in dye-sensitized solar cells (DSSCs). Adding oil to PAN increased the specific capacitance of the CNFs by 46.12% to 226.64F/g, compared with that of pure PAN CNFs. With the aid of CQDs, the short-circuit current density and photo-conversion efficiency of DSSCs increased by 25.89% and 17.08%, respectively. Mechanisms associated with the integrated valorization pathway were proposed.

Photocatalytic Hydrogen Production Using TiO2-based Catalysts: A Review.

Photocatalytic water splitting is an environmentally friendly hydrogen production method that uses abundant renewable resources such as water and sunlight. While Titanium dioxide (TiO2) photocatalyst exhibits excellent properties, its high band gap limits absorption to ultraviolet (UV) irradiation, resulting in low photo conversion efficiency. This review explores various modification techniques aimed at enhancing the efficiency of TiO2 under visible light irradiation. Factors influencing the photocatalytic water splitting reaction, such as catalyst structure, morphology, band gap, sacrificial reagents, light intensity, temperature, and potential of Hydrogen (pH)are examined. This review also summarizes different catalyst synthesis methods, and types of photocatalytic reactors, and provides insights into quantum yield. Finally, the review addresses the challenges and future outlook of photocatalytic water splitting.

Mesogenic cholesterol-naphthalene dimers: Synthesis, characterization, mesogenic properties, photochromic behaviour and theoretical insights

Synthesis and characterization of two new series of unsymmetrical dimers combining cholesterol with azo (Series I-n) or azomethine (Series II-n) naphthalene moieties were reported. The chemical structures were confirmed using FT-IR, 1H NMR, 13C NMR, mass spectrometry, and elemental analysis. Their thermotropic properties were investigated using POM, DSC and XRD. The analysis revealed that the first lower members (n = 1,2) of each series lack mesogenic properties due to short, flexible spacers, while higher members (n = 3–5,7,9,10) exhibit enantiotropic chiral nematic phases. Notably, higher members with odd spacers (n = 5,7,9) also display SmC* phases, highlighting the influence of spacer length and odd–even effects on molecular interactions. Dimers from series I-n demonstrated slightly higher clearing temperatures (TN-Iso) compared to series II-n. UV–Vis spectroscopy showed trans–cis isomerization, with a photoconversion efficiency of 56.7 % for the I-7 dimer. Computational studies using the B3LYP functional with a 6-31g (d, p) basis set provided insights into the electronic structure through electrostatic potential (ESP) and optical property analysis.

Microalgae bio-reactive façade: A model coupling weather, illumination, temperature, and cell growth over the year

This article presents the development of a numerical model coupling the thermal and biological behaviors of a microalgae biofaçade. Heat fluxes and illumination are modulated by actual weather data, and the system response is evaluated in terms of biomass and pigment production. First, the effect of the different model refinements are screened. Then, the model is applied to an illustrative case: the city of Marseille over the year 2023. The results illustrate the model’s capabilities, such as assessing the building/biofaçade thermal synergy or the summer/winter operational differences. The numerical behavior of the model is also analyzed: local and global sensitivity analyses assess the impact of uncertain parameters. The parameter inducing the highest amount of uncertainty is the microalgae photoconversion efficiency, highlighting the need to ascertain its value before designing a system. Despite this uncertainty, even under conservative assumptions, the predictions of the model are 10 % accurate.