Efficient Utilization Of Solar Energy Research Articles

Red Carbon Dots Sensitized Ni‐Doped 2D MoS2 Nanosheets as Electrode Materials for Visible‐Light Active Photorechargeable Supercapacitors

Developing photorechargeable electrochemical devices has become a new paradigm for addressing the efficient utilization of solar energy for renewable energy research. Herein, a unique 0D/2D heterostructure made of red carbon dots (RCDs) and Ni‐doped MoS2 nanosheets (NMS) has been designed as electrode materials for photorechargeable supercapacitor device. Polyvinyl alcohol (PVA) has been used as a transparent matrix for the electrode, which retains the intrinsic optoelectronic properties of the composite. Photophysical properties suggest that RCDs act as efficient light‐harvesting materials as well as visible‐light photosensitizer for the device. Suitable bandgap alignment of both counterparts facilitates the photoinduced charge separation. Finally, the composite has been utilized as a visible‐light‐sensitive photorechargeable supercapacitor device. Almost 95% of enhancement in the capacitance value has been observed under light irradiation compared to the dark condition. Furthermore, wavelength dependence device performances, photo charging, and galvanostatic discharging measurements have been investigated to analyze the overall performance of the device. The device is capable of retaining its 97.25% capacity after 1000 full cycles, suggesting its excellent photostability. The plausible mechanism for photoinduced rechargeable supercapacitance properties has been discussed in detail.

2D/2D Hydrogen-Bonded Organic Frameworks/Covalent Organic Frameworks S-scheme Heterojunctions for Photocatalytic Hydrogen Evolution.

Hydrogen-bonded organic frameworks (HOFs) demonstrate significant potential for application in photocatalysis. However, the low efficiency of electron-hole separation and limited stability inhibit their practical utilization in photocatalytic hydrogen evolution from water splitting. Herein, the novel dual-pyrene-base supramolecular HOF/COF 2D/2D S-scheme heterojunction between HOF-H4TBAPy (Py-HOF, H4TBAPy represents the 1,3,6,8-tetrakis (p-benzoic acid) pyrene) and Py-COF was successfully established using a rapid self-assembly solution dispersion method. Experimental and theoretical investigations confirm that the size-matching of two crystalline porous materials enables the integrated heterostructure material with abundant surface reaction sites, strong interaction, and an enhanced S-scheme built-in electric field, thus significantly improving the efficiency of photogenerated charge carrier separation and stability. Notably, the optimal HOF/COF heterojunction achieves a photocatalytic hydrogen evolution rate of 390.68 mmol g-1 h-1, which is 2.28 times higher than that of pure Py-HOF and 9.24 times higher than that of pure COF. These findings precisely acquire valuable atomic-scale insights into the ingenious design of dual-pyrene-based S-scheme heterojunction. This work presents an innovative perspective for forming supramolecular S-scheme heterojunctions over HOF-based semiconductors, offering a protocol for designing the powerful and strong-coupling S-scheme built-in electric fields for efficient solar energy utilization.

2D/2D Hydrogen‐Bonded Organic Frameworks/Covalent Organic Frameworks S‐scheme Heterojunctions for Photocatalytic Hydrogen Evolution

Hydrogen‐bonded organic frameworks (HOFs) demonstrate significant potential for application in photocatalysis. However, the low efficiency of electron‐hole separation and limited stability inhibit their practical utilization in photocatalytic hydrogen evolution from water splitting. Herein, the novel dual‐pyrene‐base supramolecular HOF/COF 2D/2D S‐scheme heterojunction between HOF‐H4TBAPy (Py‐HOF, H4TBAPy represents the 1,3,6,8‐tetrakis (p‐benzoic acid) pyrene) and Py‐COF was successfully established using a rapid self‐assembly solution dispersion method. Experimental and theoretical investigations confirm that the size‐matching of two crystalline porous materials enables the integrated heterostructure material with abundant surface reaction sites, strong interaction, and an enhanced S‐scheme built‐in electric field, thus significantly improving the efficiency of photogenerated charge carrier separation and stability. Notably, the optimal HOF/COF heterojunction achieves a photocatalytic hydrogen evolution rate of 390.68 mmol g−1 h−1, which is 2.28 times higher than that of pure Py‐HOF and 9.24 times higher than that of pure COF. These findings precisely acquire valuable atomic‐scale insights into the ingenious design of dual‐pyrene‐based S‐scheme heterojunction. This work presents an innovative perspective for forming supramolecular S‐scheme heterojunctions over HOF‐based semiconductors, offering a protocol for designing the powerful and strong‐coupling S‐scheme built‐in electric fields for efficient solar energy utilization.

Giant Bulk Photovoltaic Power Generation in 2D AgBiP2Se6 Crystals

AbstractWith the theoretical high power conversion efficiency (PCE) exceeding the thermodynamic Schockley–Queisser (S–Q) limit, the bulk photovoltaic (BPV) effect, which is manifested in acentric crystals across the entire visual spectrum, holds great potential for next‐generation light‐harvesting devices. Here the abnormally giant second harmonic generation (SHG) activity and BPV response in 2D AgBiP2Se6 crystals with broken inversion symmetry is demonstrated, which can be remarkably enhanced with the thickness downscaling. Based on the vertical device sandwiched with graphene electrodes, the wideband light absorption of 2D AgBiP2Se6 crystals with Eg of 1.49 eV enables giant BPV response in the entire visible spectrum, and efficient utilization of solar energy contributes to large short‐current (≈330 mA cm−2), high PCE (≈0.13%) and EQE (≈12.5%) under 532 nm light illumination. Furthermore, benefitting from the local ion redistribution driven by an in‐plane electric field, the BPV photocurrent generation is effectively enhanced 3 times, yielding an extremely high PCE of 0.18%, according high among the reported 2D acentric crystals. The study reintroduces AgBiP2Se6 to the 2D acentric crystal family and lays the groundwork to develop BPV devices for light‐harvesting applications.

Dual MPPT Algorithm Implementation in Solar Charge Controller

The implementation of a Dual Maximum Power Point Tracking (MPPT) algorithm in a solar charge controller is aimed at enhancing the efficiency of solar energy utilization. This algorithm optimizes power extraction from solar panels by dynamically adjusting the operating point to track the maximum power output under varying environmental conditions. By utilizing two MPPT trackers, the controller can efficiently handle scenarios with multiple peaks in the power-voltage curve, common in partially shaded or non-uniformly illuminated panels. This implementation involves real-time monitoring of panel voltages and currents, coupled with intelligent algorithms to swiftly respond to changes in irradiance levels. Through advanced control strategies, such as Perturbation and Observation (P&O) or Incremental Gradient (Incgrad), the system maximizes energy harvest, improving overall system performance and reliability.

Optimizing EV fast charging infrastructure: integrating high-gain interleaved converter with advanced MPPT

ABSTRACT Modernizing the Electric Vehicle (EV) charging infrastructure is essential for the widespread adoption of electric mobility. This research addresses the imperative need for enhancing the power performance of photovoltaic (PV) grid-connected inverters for EV fast charging applications. The system integrates Voltage-Oriented Control (VOC) for the PV inverter, a High-Gain Interleaved (Single Ended Primary Inductance Converter) SEPIC-Cuk (HGISC) converter, and a Bald Eagle Search Optimized Adaptive Neuro Fuzzy Inference System (BESO-ANFIS)) algorithm. VOC with Proportional Resonant (PR) ensures optimized energy transfer to grid, while the HGIBC converter enhances power performance. The proposed BESO-ANFIS Maximum Power Point Tracking (MPPT) dynamically tracks the PV array’s Maximum Power Point (MPP) under varying conditions. Additionally, a bidirectional battery converter in the energy storage system optimizes power usage. The synergistic implementation of these advanced controller results in a comprehensive solution, showcasing improved power output, grid integration, and efficient solar energy utilization for EV fast charging. MATLAB simulations and experiments demonstrate 97% efficiency and reduced Total Harmonic Distortion (THD) of 0.98%, positioning this research as an advanced solution for EV charging infrastructure enhancement.

Development and performance evaluation of a novel solar mid-and-low temperature receiver/reactor with packed metal foam

Solar-driven hydrogen production from methanol decomposition (MD) is an important method of storing solar energy as clean fuels and improving the solar energy utilization efficiency. Catalyst preparation is one of the key steps, but conventional Cu-ZnO-Al2O3 particle catalysts lead to uneven reactor temperature, reducing the efficient conversion of solar energy into fuels. To alleviate this challenge, a monolithic catalyst utilizing packed foamy copper as a carrier is developed with exceptional thermal and mass transfer properties. The experimental results validate its excellent performance in hydrogen production using MD. The absolute conversion increases by an average of 12.11 % at 250 °C and further by 14.43 % at 270 °C compared to the particle catalyst. Based on these findings, a novel solar reactor is proposed, and a multi-field coupling model is built. The comparative results verify the performance advantage of the developed solar thermochemical receiver/reactor with packed metal foam-based catalyst. It maintains high conversion rates and solar-to-fuel energy efficiency, while alleviating overheating problems caused by traditional particle catalysts. Under the design conditions, the new reactor significantly improves the absolute conversion of methanol and the energy efficiency of solar-to-fuel conversion by 4.57 % and 3.00 %, respectively, resulting in 92.64 % and 67.56 %. This study provides a theoretical basis and technical solution for more stable and efficient use of mid-and-low temperature solar energy.

Preparation and thermal stability research of oxalic acid dihydrate-glutaric acid/PAMPS phase change gel for solar thermal energy utilization

Thermal energy storage technology based on phase change materials (PCMs) can address the temporal and spatial mismatches in solar thermal energy conversion, thereby enhancing solar energy utilization efficiency. However, the liquid flow and poor thermal reliability of PCMs limit their large-scale application in solar thermal systems. In this study, we employ a simple “one-pot method” to prepare a form-stable and thermally reliable oxalic acid dihydrate-glutaric acid/poly 2-Acrylamido-2-methyl-1-propanesulfonic acid (OAD-GA/PAMPS) phase change gel. The OAD-GA/PAMPS phase change gel melts at 64.5 °C with a phase change enthalpy of 193.6 kJ/kg, the tensile strength is 7.707 MPa, and the compressive strength is 16.940 MPa. By incorporating 5 wt% BN particles, the thermal conductivity of OAD-GA/PAMPS phase change gel reaches 0.63 W/(m·K). After 200 heating-cooling cycles, the phase change temperature of the OAD-GA/PAMPS phase change gel remains nearly unchanged, and the phase change enthalpy decreases by only 5.7 %. The photo-thermal conversion efficiency of the OAD-GA/PAMPS phase change gel is 82.7 %. The high thermal reliability and photo-thermal conversion efficiency of the OAD-GA/PAMPS phase change gel makes it suitable for solar thermal energy storage applications.

Engineering hierarchical TiO2/ZnIn2S4 hybrid heterostructure with synergistic interfaces: A dual-functional S-scheme photocatalyst for efficient CO2 reduction and norfloxacin degradation

The development of multifunctional photocatalysts that can harness solar energy for both environmental remediation and energy generation is a considerable challenge in achieving sustainable development. This study introduces a dual-functional S-scheme hybrid catalyst comprising hierarchical 3D flower-like ZnIn2S4 (ZIS) microspheres embedded with TiO2 (TO) nanoparticles, synthesized via a facile in situ hydrothermal process. The unique structural and compositional synergy between ZIS and TO leverages their complementary photocatalytic properties, facilitating efficient solar energy utilization, increasing specific surface area, and enhancing CO2 adsorption capabilities. The S-scheme mechanism, confirmed by in situ-irradiated X-ray photoelectron spectroscopy and electron spin resonance spectroscopy, underlying this system promotes effective separation of photoexcited charge carriers while preserving the intrinsic strong reducibility of ZIS and high oxidizability of TO. These beneficial properties of the TO/ZIS hybrid provide a robust platform for CH4 production (75.6 μmol h−1 g−1) through selective (99.6 %) CO2 reduction over competing water reduction and achieve exceptional degradation and mineralization of the persistent antibiotic norfloxacin in water, addressing both energy and environmental challenges. Furthermore, the hybrid catalyst exhibits significant stability and recyclability, maintaining high catalytic performance across multiple cycles, thereby underscoring its practical viability. This work offers a promising blueprint for developing multifunctional photocatalysts capable of addressing critical global challenges, demonstrating the potential of hierarchical nanostructures and S-scheme charge transfer mechanisms.

Design and experimental study of solar-driven biomass gasification based on direct irradiation solar thermochemical reactor

Solar-driven biomass steam gasification is a promising technology to produce H2-rich syngas, meanwhile achieve flexible storage of renewable energy. However, the solar gasification application also faces numerous challenges, due to its involved complex chemical reaction characteristics and the inherent the multi-physics energy conversion processes. This work designs a novel direct irradiation solar gasification reactor, with the improved optical acceptance structure and reasonable test module, and the wheat straw particle is selected as experimental sample. Employing a 9 kWe high flux solar simulator, the maximum temperature of reaction bed in this prototype reactor reaches to 1260 °C, with the average solar flux of 1171.3 kW/m2. With adjustable radiation flux as experiment factor, under the highest total radiation of 3.35 kW, the molar fraction of H2 in the produced syngas is 47.1 % with the energy upgrade factor of 1.15, and the cellulose component completes decomposition. Increasing the mass flow rate of steam reduces the syngas output while raising the H2/CO ratio of the syngas. In addition, smaller biomass particle size facilitates the reaction, thereby improving the conversion efficiency of direct irradiation gasification. The investigation results provide a meaningful reference for the efficient utilization of abundant solar and biomass energy.

Dual-Functional Cs3Bi2Br9 for stable all-solid-state photo-rechargeable batteries

In light of the immense potential solid-state photo-rechargeable batteries hold in the efficient utilization of renewable solar energy, there is a rapidly growing demand for materials that possess both energy harvesting and storage capabilities. In this study, a solid-state photo-rechargeable battery has been designed based on the FTO(Fluorine-doped SnO2 transparent conductive glass)/TiO2/Cs3Bi2Br9/Pt/FTO system, which achieves dual functions of photoelectric conversion and energy storage. The inorganic bismuth-based material employed in these batteries exhibits commendable cyclic stability. Under photo-rechargeable conditions, a single cell can maintain an open-circuit voltage as high as 0.45 V in the absence of illumination. By connecting multiple cells in series, we succeed in powering an LED (Light-emitting diode) continuously for 1 min without light exposure. The findings of this research open new avenues for the design and development of novel materials that could enable highly efficient solid-state photo-rechargeable batteries.

Improved efficiency and stability of inverse perovskite solar cells via passivation cleaning

Amidst the global energy and environmental crisis, the quest for efficient solar energy utilization intensifies. Perovskite solar cells, with efficiencies over 26% and cost-effective production, are at the forefront of research. Yet, their stability remains a barrier to industrial application. This study introduces innovative strategies to enhance the stability of inverted perovskite solar cells. By bulk and surface passivation, defect density is reduced, followed by a "passivation cleaning" using Apacl amino acid salt and isopropyl alcohol to refine film surface quality. Employing X-ray diffraction (XRD), scanning electron microscope (SEM), and atomic force microscopy (AFM), we confirmed that this process effectively neutralizes surface defects and curbs non-radiative recombination, achieving 22.6% efficiency for perovskite solar cells with the composition Cs0.15FA0.85PbI3. Crucially, the stability of treated cells in long-term tests has been markedly enhanced, laying groundwork for industrial viability.

Enhanced Photothermal-Assisted Hydrogen Production via a Porous Carbon@MoS2/ZnIn2S4 Type II-S-Scheme Tandem Heterostructure.

MoS2/ZnIn2S4 flower-like heterostructures into porous carbon (PC@MoS2/ZIS) are embedded. This ternary heterostructure demonstrates enhanced light absorption across a broad spectral range from 200 to 2500nm. It features both Type-II and S-scheme dual heterojunction interfaces, which facilitate the generation, separation, and transfer of photoinduced carriers. The PC enveloped by MoS2/ZIS composite microspheres serves as a photothermal source, providing additional energy to the carriers. This process accelerates charge separation and migration, enhancing photothermal-assisted photocatalytic H2 evolution. The optimal H2 evolution rate for PC@MoS2/ZIS reaches an impressive 18.79mmolg-1h-1, with an apparent quantum efficiency of 14.1% at 400nm. This work presents a promising approach for effectively integrating multicomponent heterostructures with photothermal effects, offering innovative strategies for efficient solar energy utilization and conversion.

An Artificial Light-Harvesting System based on Supramolecular AIEgen Assembly.

Photosynthesis is a complex multi-step process in which light collection is the initial step of photosynthesis and plays an important role in the utilization of solar energy. In order to improve the utilization of sunlight, researchers have developed a variety of artificial light-harvesting systems to simulate photosynthesis in nature. Here, we report a supramolecular artificial light-harvesting system in aqueous solution. Since β-cyclodextrin (β-CD) has a hydrophobic cavity and a hydrophilic outer surface, we adopt β-cyclodextrin (β-CD) as the host molecule and use adamantane as the guest molecule. At the same time, we modified β-CD with the donor molecule naphthalimide and adamantane with the tetraphenylethylene molecule which has aggregation-induced emission (AIE) effects. By using fluorescent molecules with AIE, the self-quenching effect caused by aggregation in aqueous solution can be effectively avoided. Due to the host-guest interaction of β-CD and adamantane, nanoparticles with stable structure and uniform size can be spontaneously assembled in water. Because of the close distance and strong spectral overlap between naphthalimide and tetraphenylethylene, Förster resonance energy transfer (FRET) was realized, and artificial light-harvesting system was successfully constructed in aqueous solution. Therefore, this study provides a new strategy for constructing artificial light-harvesting system, and the artificial light-harvesting system shows broad application prospects in aqueous solutions.

Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid.

The construction of solar-to-chemical conversion system by mimicking the photosynthetic network of the chloroplast holds great promise on efficient solar energy utilization. We developed an artificial photosynthetic cell (APC) based on molecular biomimetic thylakoid (CoTPP-FePy) to split water into hydrogen and oxygen (H2 and O2) at low driving voltage (1.1 V) and neutral condition (pH≈7). The CoTPP-FePy can emulate the light reaction in thylakoids to produce O2 by coupling light harvesting, photocatalysis, and electron/energy storage (FeIII/FeII-Py). Subsequently, a membrane electrode assembly (MEA) were employed to simulate the dark reaction, wherein the proton, electron and energy generated by the light reaction can drive the H2 producing process. By a temporally and spatially coupling of the light and dark reactions, the resulting APC achieved a solar conversion efficiency of 3.1%, exceeding that of natural photosynthetic systems and demonstrating the potential of artificial photosynthesis.

Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid

The construction of solar‐to‐chemical conversion system by mimicking the photosynthetic network of the chloroplast holds great promise on efficient solar energy utilization. We developed an artificial photosynthetic cell (APC) based on molecular biomimetic thylakoid (CoTPP‐FePy) to split water into hydrogen and oxygen (H2 and O2) at low driving voltage (1.1 V) and neutral condition (pH≈7). The CoTPP‐FePy can emulate the light reaction in thylakoids to produce O2 by coupling light harvesting, photocatalysis, and electron/energy storage (FeIII/FeII‐Py). Subsequently, a membrane electrode assembly (MEA) were employed to simulate the dark reaction, wherein the proton, electron and energy generated by the light reaction can drive the H2 producing process. By a temporally and spatially coupling of the light and dark reactions, the resulting APC achieved a solar conversion efficiency of 3.1%, exceeding that of natural photosynthetic systems and demonstrating the potential of artificial photosynthesis.

Parametric optimization and energy loss analysis of a solar thermophotonic energy converter

In the present work, the model of a solar thermophotonic energy converter (STEC) is established, of which the energy balance constraint equations at both the hot and cold sides are numerically solved to uncover the dependencies of the operating temperatures of the light emitting diode (LED) and photovoltaic (PV) cell on thermal, electrical, and structural parameters. For a given band-gap 0.36 eV of the semiconductor and a concentrated factor 20 of the concentrator, the LED’s bias voltage and the PV cell’s output voltage are optimized to achieve a local maximum efficiency 13% of the STEC. Furthermore, the conditions are optimized to attain an overall maximum efficiency of 15.94%. The distributions of energy losses are presented to reveal the underlying loss mechanisms. The results obtained in this work can provide theoretical guidance for the efficient utilization of solar energy.

Highly efficient spectrum-splitting solar energy utilization based on near- and far-field thermophotovoltaics

Improving the efficiency of solar energy utilization systems is of great importance in solar energy utilization. Near-field thermophotovoltaic cells can achieve a high power density and, therefore, efficiently utilize radiative heat transfer. An efficient spectrum-splitting solar energy utilization system based on near- and far-field thermophotovoltaics was proposed. The input solar energy was divided by the splitter, and the two parts of the energy were utilized differently. The concentration ratio can determine the energy input of the system, which can affect the photoelectric conversion efficiency of the system. Further, the vacuum distance can modulate the near-field radiative heat transfer, thus significantly impacting system performance. Based on the fluctuation dissipation theorem and Maxwell's equations, a system model was constructed and calculated using the optimal design method, and the effects of these parameters were investigated. Moreover, the optimal efficiency was obtained under different operating conditions. The optimal cascade system efficiency reached 39.93 % at a concentration ratio of 3000, which was 15.59 % higher than that of a single photovoltaic system. Thus, this study proposes a method for the efficient utilization of solar energy. In addition, it provides guidance for the subsequent design and construction of spectrum-splitting cascade systems based on near- and far-field thermophotovoltaics.

Carbon-intercalated halloysite-based aerogel efficiently encapsulating phase change materials with excellent photothermal conversion and energy storage

Latent heat storage systems based on organic phase change materials (PCMs) are considered to be an efficient solar energy utilization strategy, but leakage vulnerability and insensitivity to sunlight of PCMs limit their further application in energy storage. In this work, a new hierarchical porous aerogel was constructed with the carbon intercalated halloysite nanotubes (CHNTs) as the assembly units for PCMs encapsulation to improve the load weight, stability and sunlight absorption. The CHNTs were first successfully synthesized through intercalation and carbonization, with the aim of increasing their specific surface area and sunlight absorption.Subsequently, the CHNTs/polyvinyl alcohol (PVA) aerogels with 3D honeycomb structure were prepared by self-assembly using a freeze-drying method, which can significantly promote the encapsulation ratio of lauric acid (LA) in the pores of both aerogels and CHNTs. The CHNTs can not only improve compressive strength of the aerogels and shape stability of the composite PCMs, but also enhance light absorption ability of the composites compared to pristine HNTs. As a support material, CHNTs aerogel (CHNP) loaded more than 92 wt% PCM (LA@CHNP) and exhibited an extremely high latent heat capacity (170.9 J/g). The LA@CHNP had good structural and thermal stability in 300 cycles without visible leakage. Besides, solar energy absorption increased from 43 % to 98 %, and the solar-to-thermal energy conversion efficiency increased to 95.88 %, which could be attributed to 3D porousness and carbon nanolayers of the CHNTs. We have successfully synthesized an eco-friendly and facile composite LA@CHNP, which will contribute to the design of advanced composites with excellent solar energy storage properties, and provide a new direction for the application of carbonized materials.

Prediction method of adsorption thermal energy storage reactor performances based on reaction wave model

Adsorption thermal energy storage (ATES) is one of the most important ways to achieve efficient utilization of solar energy. The lack of effective prediction methods of reactor performance severely restricts the application of the ATES system. In this paper, the prediction method of reactor performance was proposed based on the adsorption reaction wave model. The expressions between the reactor performances and the design parameters were derived by using the wave parameters of the adsorption rate wave. The mathematical relationships of design parameters-wave parameters and wave parameters-reactor performances were established, respectively. The experiments on adsorption thermal energy storage were performed, in which the zeolite-water vapor was determined as the working pairs. The air temperature and specific humidity at the inlet and outlet of the reactor were measured, and corresponding adsorption amount, thermal energy and stable output power were obtained. A comparison of the predictions for the reactor performances with experiments was carried out. The results indicated that the proposed prediction method was capable of accurately predicting the reactor performances, with a maximum deviation of less than 6.0 %. Moreover, the proposed prediction method is superior to available methods in terms of simplicity and generality.