Short-circuit Research Articles

Compatible interface based self-charging fiber for wearable electronic

With the rapid development of wearable devices, there is an increasing demand for flexible, eco-friendly, and reliable power sources. The self-charging energy system, which integrates energy collection and storage, has emerged as one of the most promising sustainable energy sources, with an urgent need for its application and implementation. In this work, we proposed a fiber-shaped self-charging system based on supercapacitor (SC) and triboelectric nanogenerator (TENG). For the supercapacitor, a silver-decorated carbon fiber with PEDOT: PSS coated is used as the positive electrode, while carbon nanotube film/Fe2O3/MoS2 serves as the negative electrode. The assembled coaxial structure not only shortens the distance between the positive and negative electrodes, effectively improving charge transfer efficiency, but also ensures the flexibility and mechanical stability of the device. The designed supercapacitor exhibited a capacitance of 213.3 mF cm−2 and demonstrated excellent stability of 92 % retention rate even after 5000 cycles. Moreover, the negative electrode of the supercapacitor also serves as a compatible interface for the TENG, with silicone rubber coating acting as the friction layer, forming a single-electrode structure. This coaxial structure with a compatible interface allows for higher efficiency in charge capture and transfer, doubling the charging efficiency compared to incompatible structures, while also ensuring flexibility, making it more suitable for wearable applications. By weaving the TENG, it exhibits an open-circuit voltage of 150 V, a short-circuit current of 6 μA, and a high power density of 900 mW cm−2. In addition, it can also serve as a self-powered sensor, capable of accurately detecting human motion and current conditions. This research proposes an effective compatible interface architecture promising application prospect for advancing sustainable development of self-powered wearable electronic devices.

The improvement of electrochemical performance by mixing InF3 in Li5.3PS4.3Cl1.7 solid electrolyte

All-solid-state batteries (ASSBs) employing solid electrolytes (SE) are currently gaining attention as next-generation energy storage devices. Solid electrolytes exhibit higher energy densities and operation across a wide temperature range than liquid electrolytes. The solid electrolyte acts as a separator, providing higher mechanical strength than polymer separators. This helps prevent cell deterioration and short circuit issues caused by lithium dendrite growth during charge – discharge cycles. Consequently, lithium metal, previously challenging to apply in conventional lithium-ion batteries, can be utilized as an anode electrode material. Sulfide-based solid electrolytes offer advantageous mechanical properties and high ionic conductivity. However, their narrow chemical/electrochemical stability window poses challenges. During the charging-discharging process of a battery with a lithium metal anode, a reduction decomposition reaction of the solid electrolyte occurs. On the other hand, Lithium Fluoride (LiF) exhibits low electronic conductivity due to a wide band gap but has a broad electrochemical stability window. In this study, we prepared a mixture of Li5.3PS4.3Cl1.7 with InF3 to generate an artificial solid electrolyte interphase (SEI) containing LiF. We confirmed the structural properties using powder X-ray diffraction (XRD). The XRD pattern showed the maintenance of the argyrodite structure, with only an increase in the peak intensity corresponding to InF3. The optimized solid electrolyte-based ASSB demonstrated a higher initial discharge capacity of 172.8 mAh/g, a coulombic efficiency of 78.54 %, and a capacity retention rate of 93.6 %, outperforming ASSBs based on the bare solid electrolyte (Li5.3PS4.3Cl1.7).

Identification System for Short-Circuit Fault Points in Concentrated Stator Windings of Motors

Motors serve as the primary power sources in a wide range of industrial fields. In recent years, their application has been expanded to electric and hybrid electric vehicles. As the performance of the motors installed in electric vehicles directly affects human life, it is critical to diagnose the condition of the windings. The objective of this article is to establish a method to identify the short-circuit fault points in concentrated stator windings based on the magnetic flux density distribution near the stator windings. Unlike with distributed windings, the coils are wound around the teeth in concentrated windings. Thus, it is expected that the accurate position specification of the short circuit can be realized if a detailed magnetic flux density distribution over the teeth is obtained with an appropriate magnetic field sensor. The problem of sensor positioning is solved with two stepper motors moving the search coil in the rotational and longitudinal directions independently at specified intervals. The excellent capability of the proposed system is verified through experiments using the stator winding employed in hybrid electric vehicles. The accuracy and sensitivity of the proposed identification system for short-circuit fault points may enable its practical application in industries, for example, shipping and periodic inspections as well as the production management of motors with concentrated stator windings.

Agroecology: A Promising Path Towards the Sustainable Transition of Food Systems

Objective: Uncover the transformative potential of agroecology in shaping sustainable food systems, with a particular focus on its pivotal role in transitioning from conventional systems to sustainable practices rooted in agroecological principles. Theoretical Framework: The current scenario presents alternatives to industrial agriculture, which prioritizes mass food production for global markets. In this context, agroecology emerges as a beacon of hope, championing short marketing circuits, fair trade, and a deep respect for local culture and the environment. The sharing of agroecological experiences, particularly in the context of family farming, offers a promising path toward agricultural systems that diverge from the traditional industrial model. Method: The systematic review used scientific articles published between 2011 and 2023, selected from the Web of Science and ScienceDirect databases. Results and Discussion: Agroecological production systems present themselves as a viable alternative to industrial agriculture, demonstrating that agroecological principles have the potential to promote healthier and more sustainable agri-food systems. Family farming plays a crucial role in this context, meeting the goals of agroecology. Research Implications: It highlights the promising role of agroecology in promoting family farming by achieving sustainable food production and supporting the demand for healthier foods. Originality/Value: This paper contributes to understanding the relationship between agroecology and agri-food systems, providing insights into agroecological practices, including sustainability in food production.

An Anthocyanin-Based Eco-Friendly Triboelectric Nanogenerator for pH Monitoring and Energy Harvesting.

In recent years, renewable and sustainable triboelectric nanogenerators have attracted attention due to their high energy conversion rate, and enhancing their functionality further contributes to their applicability across various fields. A pH-sensitive triboelectric nanogenerator (pH-TENG) has been prepared by electrostatic spinning technology, with anthocyanin as the pH indicator and environmentally friendly polyvinyl alcohol (PVA) as the substrate. Among many friction-negative materials, the pH-TENG exhibits the best combination with fluorinated ethylene propylene (FEP) and yields an open-circuit voltage of 62 V, a short-circuit current of 370 nA, and a transferred charge of 21.8 nC. At a frequency of 3 Hz, it can charge a 4.7 μF capacitor to 2 V within 45 s, effectively powering a thermometer. Furthermore, the presence of anthocyanin does not affect the pH-TENG's power generation performance and enables the monitoring of a wide range of environmental pH changes, with an ΔE change of 28.8 ± 7.6. Therefore, pH-TENG prepared with environmentally friendly materials can bring new available materials to the biological and medical fields.

Self-Powered Biomimetic Pressure Sensor Based on Mn-Ag Electrochemical Reaction for Monitoring Rehabilitation Training of Athletes.

Self-powered pressure detection using smart wearable devices is the subject of intense research attention, which is intended to address the critical need for prolonged and uninterrupted operations. Current piezoelectric and triboelectric sensors well respond to dynamic stimuli while overlooking static stimuli. This study proposes a dual-response potentiometric pressure sensor that responds to both dynamic and static stimuli. The proposed sensor utilizes interdigital electrodes with MnO2/carbon/polyvinyl alcohol (PVA) as the cathode and conductive silver paste as the anode. The electrolyte layer incorporates a mixed hydrogel of PVA and phosphoric acid. The optimized interdigital electrodes and sandpaper-like microstructured surface of the hydrogel electrolyte contribute to enhanced performance by facilitating an increased contact area between the electrolyte and electrodes. The sensor features an open-circuit voltage of 0.927V, a short-circuit current of 6µA, a higher sensitivity of 14mV/kPa, and outstanding cycling performance (>5000 cycles). It can accurately recognize letter writing and enable capacitor charging and LED lighting. Additionally, a data acquisition and display system employing the proposed sensor, which facilitates the monitoring of athletes' rehabilitation training, and machine learning algorithms that effectively guide rehabilitation actions are presented. This study offers novel solutions for the future development of smart wearable devices.

A method for determining the location and type of fault in transmission network using neural networks and power quality monitors

A new technique for identifying the location of a fault on a power line utilizing neural networks is presented in this paper. Specifically, the procedure involves four stages (three of which employ neural networks): gathering voltage input data via simulation, classifying the fault type, detecting the faulted line, and determining the fault position on the power line. This model was developed and tested for the IEEE 39 bus test system. Input voltages are obtained using DigSILENT PowerFactory software in which a set of three-phase and single-phase short circuits are simulated. Not voltages from all buses are used for the subsequent stages, only voltages from the optimally placed 12 buses in the IEEE 39 bus test system are used. In the second step, the first neural network is employed in order to classify the fault type – single-phase or three-phase. In the second stage, another neural network is used to determine the faulted line and in the third stage, the last neural network is developed to determine the fault position on the faulted line.

Building Bulk and Interface Dual Fast Li+ Conducting Pathway in Composite Solid Polymer Electrolyte Membrane for All–Solid–State Lithium–Metal Batteries

AbstractSolid polymer electrolytes (SPEs) are considered a promising solution to the safety problems of lithium‐ion batteries (LIBs) using liquid electrolytes. However, the high crystallinity and low ionic conductivity hinder the practical application of SPEs. Herein, we design a composite solid polymer electrolyte with a dual fast Li+ conducting pathway in bulk and interface by incorporating highly Li+ conductive ceramic Li6.4Ga0.2La3Zr2O12 (LGLZO) in polyethylene oxide (PEO)/Li–bis (trifluoromethanesulfonyl) imide (LiTFSI) system. Compared to Li6.5La3Zr1.5Ta0.5O12 (LLZTO), LGLZO provides better Li+ conductivity; therefore, a fast Li+ conducting pathway will form in the bulk of LGLZO nanofillers. Besides, LGLZO nanofiller accelerates the dissociation of LiTFSI and benefits the transfer of free Li+ through the SPEs near the LGLZO surface, forming another interface fast Li+ conducting pathway in the SPEs. Benefits from the dual fast Li+ pathway design, the composite electrolyte membrane with 15 wt % LGLZO nanoparticles presents a high ionic conductivity of 8.0×10−4 S cm−1 at 60 °C. The Li−Li symmetric cells with optimized content LGLZO show good cycling stability (no short circuit even after 1000 h), and the all–solid Li/LiFePO4 batteries exhibit excellent cycling performance (remained 154 mAh g−1 after 500 cycles at 0.2 C under 60 °C).

A theoretical review of passivation technologies in perovskite solar cells

Perovskite solar cells have demonstrated remarkable progress in recent years. However, their widespread commercialization faces challenges arising from defects and environmental vulnerabilities, leading to limitations in energy conversion efficiency and device stability. To overcome these hurdles, passivation technologies have emerged as a promising avenue. These passivators are strategically applied at the interface between perovskite absorbers and charge transport layers to mitigate the adverse effects of defects and environmental factors. While prior reviews have predominantly focused on experimental observations, a comprehensive theoretical understanding of the passivators has been lacking. This review focuses on recent advancements in first-principles density functional theory studies that delve into the fundamental properties of passivators and their intricate interactions with perovskite materials and charge transport layers. By exploring the atomic-level roles of passivators, this review elucidates their impact on critical parameters such as open circuit voltage (Voc ), short circuit current density (Jsc ), fill factor, and the overall stability of perovskite solar cells. The synthesis of theoretical insights from these studies can serve as guidelines for the molecular design of passivators with the ultimate objective of advancing the commercialization of high-performance perovskite solar cells.

Ultra-stretchable and anti-freezing ionic conductive hydrogels as high performance strain sensors and flexible triboelectric nanogenerator in extreme environments

Conductive hydrogels have shown promising applications in a variety of portable smart wearable electronics and flexible sensors due to their high flexibility, stretchability, adjustable mechanical properties and excellent electrical conductivity. However, most of the current hydrogel-based flexible strain sensors and portable triboelectric nanogenerator (TENG) generally suffer from low stretchability/flexibility, poor mechanical properties, weak low-temperature tolerance and low power output. Herein, a multifunctional ionic conductive hydrogel (PPAVC-BA) with ultra-stretchability (∼1750%), high transparency (85%), high electrical conductivity (13.7 mS/cm), and outstanding anti-freezing properties (below −80°C without freezing). The strain sensor assembled from the PPAVC-BA hydrogel shows high sensitivity (GF=4.43) and ultra-wide sensing detection range (0%-1100%) as well as fast response time. Based on these properties, the PPAVC-BA hydrogel strain sensor can accurately recognize different joint movements of the human body as well as weak muscle beats. In addition, the PPAVC-BA hydrogel-based TENG (PPAVC-BA-TENG) exhibits excellent electrical output performance, with an open circuit voltage (Voc) of about 420 V, a short circuit current (Isc) of 23 μA, a short-circuit transfer charge (Qsc) of 112 nC and a maximum power density of 2246.03 mW/m2, which allows it to power small electronic devices. This PPAVC-BA-TENG also shows outstanding tensile performance and can output stable electrical signals at 200% strain. Impressively, the PPAVC-BA-TENG exhibits good electrical output performance even at low temperature of −50°C and high temperature of 80°C. The flexible strain sensors and stretchable TENG for high performance and multifunctionality reported in this work provide viable references in the development of motion detection, energy harvesting and self-powered electronic devices.

Unveiling the potential of lead-free Cs2AgBiBr6 (CABB) perovskite for solar cell application

The remarkable structural stability and optoelectronic properties of Cs2AgBiBr6 (CABB) material have positioned it as a highly appealing candidate for the solar cell application. The research focused on modeling and examination of perovskite solar cells utilizing Cs2AgBiBr6 as the active material, incorporating various electron transport layers (ETL) and hole transport layers (HTL). The device structure comprised of ITO/ZnO:Al/ZnO/Cs2AgBiBr6/Cu2O/Au. This optimized device, shows Voc = 1.67 V, Jsc = 15.52 mA/cm2, fill factor (FF) = 71.32 %, and conversion efficiency = 18.5 %. Active layer defects and trap charges at the interface of the CABB layer can trap photo generated electrons and holes, permitting higher carrier recombination. That reduces both open circuit voltage and short circuit current density. The conversion efficiency deteriorates from 18.5 % to 2.65 % when the defect density increases from 1 × 1010/cm3 from 1 × 1016/cm3. Also trap charges and multiple trap charges play a vital role in the performance of the CABB solar cell.

Fabrication, characterization and application of W/N co-doped zinc oxide nanoparticles as a promising photoanode for dye-sensitized solar cells

In the present investigation, undoped, W doped, and W/N co-doped ZnO nanoparticles were prepared by sol–gel route. Here, the ZnO layers were fabricated via the doctor blade method. Hexagonal wurtzite structure is determined by XRD studies. The formation of a hexagonal wurtzite structure was observed from X-ray powder diffraction (XRD) resulting in a slight increase in crystallite size with an increase in doping content. The UV observation shows that W/N co-doping shifted the absorption spectra towards a higher wavelength and reduces the band gap energy. The EDS spectra confirms the high purity and triumphant doping of the W(tungsten) and N(nitrogen) into the ZnO lattice. The morphology of undoped and W/N co-doped ZnO nanoparticles was demonstrated by using FESEM and HRTEM. The 2 % W and 1.5 % N co-doped ZnO photoanode based DSSC (dye-sensitized solar cells) gained the highest short circuit current density of 8.44 mAcm−2 having an open-circuit voltage of 0.65 V, and PCE (power conversion efficiency) of 3.60 %.

Asymmetric ionogel electrolyte with an ultrathin metal–organic framework layer for lithium dendrite inhibition in solid-state lithium-metal batteries

Solid-state electrolytes (SSEs) are used to prevent internal short circuits caused by the growth of lithium dendrites in solid-state lithium-metal batteries (SSLMBs). Ionogel electrolytes are new polymeric SSEs with outstanding processability, excellent flexibility, and superior ionic conductivity. Lithium-ion transport in ionogel electrolytes depends on ionic liquid (IL) content; however, increasing the IL content improves ionic conductivity but sharply decreases mechanical properties, thus limiting the ability to resist lithium dendrites. Thus, ionogel electrolytes must strike a balance between ionic conductivity and mechanical properties. Herein, we adopt a new strategy to suppress the growth of lithium dendrites by in situ polymerizing an ultrathin metal–organic framework (MOF) layer (9.8 μm) onto a highly ionic conductive ionogel electrolyte. The ionogel electrolyte provides an asymmetric SSE (ASSE) with a remarkable ionic conductivity of 4.8 × 10−4 S cm−1 (30 °C), whereas the ultrathin MOF layer regulates uniform dissolution/deposition of lithium and inhibits lithium dendrite growth, thereby increasing critical current density of the ASSE to 0.65 mA cm−2. An SSLMB assembled with the ASSE and LiFePO4 exhibits excellent performance and cycling stability, maintaining a specific capacity of 125.4 mAh g−1 after 500 cycles at 0.3C.

Ultrasonic assessment of aging in lithium metal pouch cells

Lithium metal anodes are prone to non-uniform lithium plating that can lead to dendrite formation, internal short circuits, and catastrophic ignition. This type of structural defect is not captured by battery management systems, prompting the need to advance nondestructive evaluation (NDE) techniques that are suitable for periodic monitoring of the internal structure. An ultrasonic inspection technique is evaluated here as a means of identifying flaws and irregular lithium plating that can be a precursor to dendrite formation and, ultimately, battery failure.Lithium metal pouch cell batteries were aged through electrochemical cycling at a range of moderate constant-current charging and discharging rates. They were inspected intermittently using a tailored local ultrasonic resonance spectroscopy (LURS) approach that measures the local through-thickness resonances of the battery as an indicator of the underlying structure. LURS results showed clear structural resonances in cells in the range of 3–7 MHz, which shifted significantly to lower frequencies as batteries aged. In addition to point measurements, scanning LURS measurements were implemented to map resonance frequencies over the electrode surface. These resonance maps revealed spatial variations in structure that developed during aging and showed better contrast to structural variation than achieved using conventional amplitude-based c-scans of the specimens.NDE results from pouch cell measurements were compared to a destructive physical analysis of the electrode structures using scanning electron microscopy (SEM). The SEM results showed differences in the end-of-life lithium anode structure at different charge rates. The results of this study show the capability of LURS as a means for identifying changes in battery structures during aging and establish resonance trends that may be applied in future work for prognostic modeling of batteries in service.

Dynamic Anion Enables Self‐Healing Single‐Ion Conductor Polymer Electrolyte for Lithium‐Metal Batteries

AbstractLithium‐metal batteries (LMBs) are regarded as a promising option for high‐energy‐density storage systems. However, lithium dendrite growth in LMBs can damage electrolytes and cause short circuits, which severely limits the practical application of LMBs. It is highly desired to develop an advanced polymer electrolyte with self‐healing capability and the ability to inhibit the growth of lithium dendrites for enhancing safety and prolonging the cycle life of the LMBs. Herein, sp3 boron‐based single‐ion conductor polymer electrolytes (B‐SIPEs) with excellent self‐healing capability and interfacial stability are constructed. The rapid bond exchange reactions of dynamic borate anions enable B‐SIPE to fast self‐heal in mild conditions, with a high self‐healing efficiency of 87% within 30 min at an ambient temperature. In particular, B‐SIPE displays a high Li+ transference number (0.88) and excellent lithium dendrite inhibition ability. The Li|B‐SIPE|Li cells exhibit a stable overpotential over 2000 h without short‐circuit. Additionally, the LiFePO4||Li cells with B‐SIPE exhibit superior long‐term cycling performance, with 93.5% capacity retention for 500 cycles. Significantly, B‐SIPE is capable of self‐healing the fracture in LiFePO4||Li cells and recovering the battery performance. These results demonstrate that the advanced self‐healing single‐ion conductor polymer electrolytes effectively promote the reliability and safety of LMBs.

Influence of Proteolytic Cleavage of ENaC's Gamma Subunit upon Na+ and K+ Handling.

The ENaC γ subunit is essential for homeostasis of Na+, K+, and body fluid. Dual γ subunit cleavage before and after a short inhibitory tract allows dissociation of this tract, increasing channel open probability (PO), in vitro. Cleavage proximal to the tract occurs at a furin recognition sequence (143RKRR146, in the mouse γ subunit). Loss of furin-mediated cleavage prevents in vitro activation of the channel by proteolysis at distal sites. We hypothesized that 143RKRR146 mutation to 143QQQQ146 (γQ4) in 129/Sv mice would reduce ENaC PO, impair flow-stimulated flux of Na+ (JNa) and K+ (JK) in perfused collecting ducts, reduce colonic amiloride-sensitive short circuit current (ISC), and impair Na+, K+, and body fluid homeostasis. Immunoblot of γQ4/Q4 mouse kidney lysates confirmed loss of a band consistent in size with the furin-cleaved proteolytic fragment. However, γQ4/Q4 male mice on a low Na+ diet did not exhibit altered ENaC PO or flow-induced JNa, though flow-induced JK modestly decreased. Colonic amiloride-sensitive ISC in γQ4/Q4 mice was not altered. γQ4/Q4 males, but not females, exhibited mildly impaired fluid volume conservation when challenged with a low Na+ diet. Blood Na+ and K+ were unchanged on a regular, low Na+, or high K+ diet. These findings suggest that biochemical evidence of γ subunit cleavage should be used in isolation to evaluate ENaC activity. Further, factors independent of γ subunit cleavage modulate channel PO and the influence of ENaC on Na+, K+, and fluid volume homeostasis in 129/Sv mice, in vivo.

Application of depth feature recognition technology in foreign object recognition in distribution network monitoring video

Foreign objects identification in the distribution network is an important link in the security of electric power, and is of great significance to the normal transportation of electric power. At present, a lot of equipment in the distribution network is in the open air environment, facing a large number of foreign interference. These foreign objects not only bring potential safety hazards to the distribution network, but also easily lead to short circuit, causing power supply difficulties within the region. Therefore, the research first constructs an optimized triplet feature learning model. On this basis, the HOG-SVM depth feature recognition model is proposed. In HOG-SVM, AM is introduced to improve recognition accuracy. In addition, the research enhances the night vision ability of the model by standardizing the features in the image region block. The results show that the AP of the model is stable at more than 90.54%, the average FPR is 2.21%, and the average FNR is 3.17%. The performance of HOG-SVM is significantly better than that of traditional SVM. It verifies the contribution of this research in the field of foreign object recognition and application value in ensuring the security of distribution network.

Microwave treated dye from seeds of Syzygium cumini for the photogeneration of charge carriers and consistency of the fabricated dye sensitized solar cell

In this work, aid of microwaves has been used for the ethanolic extract of the dyes from the seeds of syzygiumcumini. The dye served as a good sensitizer in the photoanode of dye sensitized solar cell as it has greater affinity to have anchoring effect with the TiO2 coated over FTO substrate. The photoexcitation of the anthocyanin present in the dye has engendered electronic excited states to promote the electron transfer into the semiconductor oxide (TiO2) material. The key lead of the dye is the production of electronic excited states with the energy equal to that of the conduction band of TiO2. Basic characterization of FTIR and UV–Visible spectroscopy for the dye has been done and SEM photograph has been taken for the photoanode of the fabricated DSSC. The fabricated solar cell with the photoanode, graphite-based counter electrode and I−/I3− electrolyte has been tested for JV characteristics. The cell has given efficiency of 1.85 % with fill factor, open circuit voltage, short circuit current density, maximum voltage and maximum current of 0.808219, 0.9921V, 2.314 mA/cm2 0.8865V and 2.093 mA/cm2.

Proton diffusion in two model grain boundaries of monoclinic zirconia

To bring new insights into the mechanisms governing the hydrogen diffusion within the monoclinic zirconia layer formed on the fuel rods of nuclear pressurized water reactors, we model at the atomic scale two grain boundaries using ReaxFF, an interatomic potential. We study the behavior of protons within these two grain boundaries and find a strong proton stabilization compared to the bulk of zirconia, in accordance with the experimental observations from literature of an overconcentration in the oxide layer grain boundaries. We tackle the proton diffusion mechanisms, considering a substantial number of migration barriers. The obtained migration energies are higher in the grain boundaries than in the bulk. This indicates that the protons diffuse more slowly within the grain boundaries of monoclinic zirconia than within the bulk. Thus, the simulated grain boundaries act more as traps rather than as diffusion short circuits.

Active cooling of a photovoltaic module in hot-ambient temperatures: theory versus experiment

Abstract The performance improvement of a PV-module is investigated theoretically and experimentally in a long-term research-plan via module cooling by different approaches including passive, active, and evaporative cooling as well as water cooling for the same module. In the present paper, the investigation is conducted to decide on the suitability of active-cooling of the module in hot-ambient temperatures. A module without cooling is used as a base case for comparison against cooled modules with and without fins attached to the module’s rear-surface and extended down in an air-cooling duct underneath the module. At first, a theoretical study of heat transfer through the module is conducted to investigate how the calculated cell temperature and module output power are influenced by the air velocity from a blower, ambient temperature and solar irradiation. The results showed a decrease of cell temperature by about 7–10 °C with a subsequent increase of electrical efficiency. The cell temperature decreases significantly with the increase of duct height and with the increase of the number and length of fins, the same as in passive cooling. The cell temperature decreases by more than 3 °C at duct height of 0.2 m. The calculated values of cell temperature, open-circuit voltage and short-circuit current of the module with and without active cooling agreed reasonably with the present measured values over the day hours of two successive days in summer season. At air velocity of 1.5 m/s, the increase of electrical efficiency by active cooling was found 0.67–0.80 %. Further increase of air-flow velocity or duct-height in active cooling seeking higher efficiency is not recommended due to increase of consumed electric power by air-blower and limited decrease of cell temperature. This concludes that air cooling is not effective in regions of hot ambient temperatures. For a non-cooled module, the cell temperature is related to the ambient temperature in terms of the solar radiation and NOCT, the datasheet value of normal-operating-cell-temperature. The relationship is modified in the present paper to account for air-flow through the duct seeking its extension for application to air-cooled modules.