SmartHelio

Description

SmartHelio est une société de technologie spécialisée dans l'analyse solaire avancée et les solutions de maintenance prédictive pour les centrales photovoltaïques solaires. Leurs algorithmes d'IA propriétaires, éclairés par la physique, peuvent détecter et prédire plus de 30 failles différentes en temps réel avec une précision de 95 %, ce qui aide à prévenir les problèmes potentiels avant qu'ils ne se produisent. En intégrant la prévision climatique et l'analyse des données profondes, SmartHelio propose des outils pour réduire les risques d'investissements solaires et maximiser la production d'énergie. Confiés par une clientèle mondiale diversifiée, les solutions logicielles de SmartHelio visent à optimiser l'échelle des actifs solaires, l'efficacité opérationnelle et l'atténuation des changements climatiques.

Source officielle

https://smarthelio.com

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Catégories associées (4)

Concepts associés (22)

Cours associés (34)

Séances de cours associées (458)

MOOCs associés (2)

Personnes associées (59)

Publications associées (14)

Start-ups associées (5)

Unités associées (10)

Panneau solaire

Le terme « panneau solaire » peut faire référence à plusieurs concepts liés à l'énergie solaire : capteur solaire photovoltaïque : aussi appelé panneau solaire photovoltaïque, convertit le rayonnement solaire en électricité par effet photovoltaïque ; capteur solaire thermique : aussi appelé panneaux solaire thermique, convertit le rayonnement solaire en chaleur et la transfère à un fluide caloporteur ; panneau photovoltaïque thermique : combinaison des deux précédents ; panneau solaire aérothermique : métho

Énergie solaire

Lénergie solaire est la fraction de l'énergie électromagnétique provenant du Soleil, traversant l’atmosphère qui en absorbe une partie, et parvenant à la surface de la Terre. L'énergie solaire est à l'origine du cycle de l'eau, du vent et de la photosynthèse réalisée par le règne végétal, dont dépend le règne animal via les chaînes alimentaires. Le Soleil est à l'origine de la plupart des énergies sur Terre, à l'exception de l'énergie nucléaire et de la géothermie profonde.

Solar power

Solar power is the conversion of energy from sunlight into electricity, either directly using photovoltaics (PV) or indirectly using concentrated solar power. Photovoltaic cells convert light into an electric current using the photovoltaic effect. Concentrated solar power systems use lenses or mirrors and solar tracking systems to focus a large area of sunlight to a hot spot, often to drive a steam turbine.

Photovoltaic system

A photovoltaic system, also PV system or solar power system, is an electric power system designed to supply usable solar power by means of photovoltaics. It consists of an arrangement of several components, including solar panels to absorb and convert sunlight into electricity, a solar inverter to convert the output from direct to alternating current, as well as mounting, cabling, and other electrical accessories to set up a working system. It may also use a solar tracking system to improve the system's overall performance and include an integrated battery.

Cellule photovoltaïque

Une cellule photovoltaïque, ou cellule solaire, est un composant électronique qui, exposé à la lumière, produit de l’électricité grâce à l’effet photovoltaïque. La puissance électrique obtenue est proportionnelle à la puissance lumineuse incidente et elle dépend du rendement de la cellule. Celle-ci délivre une tension continue et un courant la traverse dès qu'elle est connectée à une charge électrique (en général un onduleur, parfois une simple batterie électrique).

Photo‐Electrochemical Conversion of CO 2 Under Concentrated Sunlight Enables Combination of High Reaction Rate and Efficiency

Sophia Haussener, Silvan Suter, Etienne Boutin, Mahendra Patel

Photo-electrochemical production of solar fuels from carbon dioxide, water, and sunlight is an appealing approach. Nevertheless, it remains challenging to scale despite encouraging demonstrations at low power input. Higher current densities require notable voltage input as ohmic losses and activation overpotentials become more significant, resulting in lower solar-to-CO conversion efficiencies. A concentrated photovoltaic cell is integrated into a custom-made heat managed photo-electrochemical device. The heat is transferred from the photovoltaic module to the zero-gap electrolyzer cell by the stream of anodic reactant and produce synergetic effects on both sides. With solar concentrations up to 450 suns (i.e., 450 kW m−2) applied for the first time to photo-electrochemical reduction of CO2, a partial current for CO production of 4 A is achieved. At optimal conditions, the solar-to-CO conversion efficiency reaches 17% while maintaining a current density of 150 mA cm−2 in the electrolyzer and a CO selectivity above 90%, representing an overall 19% solar-to-fuel conversion efficiency. This study represents a first demonstration of photo-electrochemical CO2 reduction under highly concentrated light, paving the way for resource efficient solar fuel production at high power input.

Wiley2022

Composition and Interface Engineering of High Performing Perovskite Solar Cells

Mousa Abdulla M E Abuhelaiqa

Perovskite solar cells have been established as a disruptive technology in the domain of photo-voltaics. Their facile, low-temperature processing and high-power conversion efficiency make them stand-out among other mature solar technologies. The performance of perovskite solar cells is pro-foundly tied to an interplay of material properties of singular thin films that are assembled to form the photovoltaic device stack. An understanding of optoelectronic, morphological, and other key charac-teristics of each layer and its interfaces is instrumental in advancing the science of perovskite solar cells. Since their inception after just over a decade, much work on perovskite solar cell has been stag-nant to bring the technology to the market. The long-term stability remains foremostly the main hin-drance to facilitating technology transfer. Therefore, the work presented in this thesis explores multi-ple interface and compositional approaches to promote stability and other photovoltaic parameters of perovskite solar cells.In the second chapter of the thesis, a light-soaking exploration was done on perovskite sam-ples that utilize single (TiO2 and SnO2) and bilayered (TiO2/SnO2) electron transporting materials. The work aims to expand consensus on the optoelectronic and morphological features of light-soaked samples and link them with long-term stability. Upon preliminary testing, maximum power point tracking on each sample reveals efficiency preservation of SnO2 and TiO2/SnO2 samples over the course of 1000 hours while prominent degradation was revealed for the TiO2 sample. On a secondary investigation, light-soaking characterizations were performed where fresh and light-soaked samples were characterized to obtain photoluminescence, microscopic, and crystallographic features. The work reveals the added benefit of employing TiO2/SnO2 transporting bilayers to improve both the stability and power conversion efficiency of a perovskite solar cell. Building on an effort to understand TiO2/SnO2 bilayer behaviors, the third chapter investigates the role of halide passivating elements in SnO2 on the performance of perovskite solar cells. The study utilizes three metalorganic precursors based on acetylacetone complexes with chloride and bromide groups to fabricate SnO2 layers at different annealing temperatures. Upon thermal and elemental in-vestigations, the study clearly links the presence of amorphous halide elements in SnO2 to the power conversion efficiency of perovskite solar cells. More-in-depth, the optimal SnO2 annealing tempera-ture for bromide containing samples 250 ï°C compared with 220 ï°C for chloride containing samples. The higher temperature tolerance tendency was correlated to bromideâs lower sublimation sensitivity. Overall, the study highlights the importance of amorphous passivating elements in SnO2 for high per-forming planar perovskite solar cells. Finally, the fourth chapter involves a novel cation mixing approach for 2D perovskites at the interface of the 3D perovskite and the hole transporting layer. Alkyl ammonium halides have been widely used to form light-stable 2D perovskite films upon interaction with excess PbI2. In this study, different alkyl chain cations (propylammonium iodide and octylammonium iodide) were mixed in one solution to form a novel 2D perovskite crystal lattice. Photoluminescence and x-ray diffraction spec-troscopy investigations reveal a unique crystal lattice and a uniform quasi-2

EPFL2022

Renewable energy deployment and implementation of a circular economy will play a crucial role in decreasing CO2 emissions to meet the target from the Paris agreement. Dye-sensitized solar cells (DSSCs) can be designed in various colors and transparency for building-integrated photovoltaics (BIPV). This emerging technology has gained significant attention for its remarkably high power conversion efficiency (PCE) under indoor lighting up to 34%. To improve the performance of DSSCs, various approaches to study and reduce the interfacial electron recombination from the conduction band of the semiconductor to the electrolyte were implemented in this thesis. One of the approaches was the design of a tandem electrolyte containing two redox species, the radical AZADO (AZ+/0) and the [Co(bpy)3]2+/3+ complex. DSSCs with tandem electrolytes showed increased open-circuit voltage (VOC) up to 1009 mV and enhanced PCE of 9.15%. The VOC enhancement was determined to result from the higher redox potential of (AZ+/0) and the slower electron recombination rate. These findings demonstrate the advantages of employing tandem electrolytes to improve the VOC and overall performance of DSSCs. To decrease the solvent's volatility and the interfacial electron recombination in cobalt-based electrolytes, hyperbranched networks (HB) were designed through a click thiol-ene reaction between a thiol-siloxane and an acrylate monomer. The formed polymers were denoted HB1 (thiol-siloxane and PEGMA) and HB2 (thiol-siloxane and PEGMA). The addition of 20% of HB polymers to a cobalt-based electrolyte retained up to 98% of their initial weight until 150°C. The devices employing 10%(v/v) of HB1 attained the highest PCE under AM1.5 of 8.52%, comparable to 9.36% for the cobalt reference electrolyte. All the HB-electrolytes presented higher VOC values than the cobalt reference due to an upward shift in the CB of TiO2 and longer electron lifetimes. It was determined that the HB-polymers reduce the electron recombination and enhance the photovoltaic performance under low light intensity leading to a PCE of 23.19% under 1000 lux compared to 20.37% for the Co-reference. We then developed a new dye, R7, with a strong electron-donating PAH core and BPT2 as the central building block and a bulkier HF donor to decrease electron recombination at the interface TiO2/electrolyte. We found that in the presence of a copper electrolyte, the dye R7 outperformed devices with R6. EIS revealed that the bulky HF-donor introduction effectively suppressed the electron recombination between the TiO2 surface and the redox shuttle. Additionally, we employed a co-sensitized system of R7+Y123 to reach the outstanding parameters of JSC of 16.15 mAcm-2, VOC of 1035 mV, FF of 0.76 to achieve a top PCE of 12.7%. To the best of our knowledge, this is the highest for copper-based DSSCs using a blue photosensitizer. Lastly, the interfacial phenomena in DSSCs with carbon counter electrodes (CCEs) and copper-based electrolytes were studied to determine the feasibility of the production of monolithic DSSCs with copper-based hole-transporting materials. It was found that the electron transport in devices with CCEs is in the same order of magnitude as those with PEDOT. However, the devices with CCEs presented a decrease of 2 orders of magnitude in the recombination resistance, resulting in decreased VOC and JSC, leading to a PCE of 17% compared to 24.5% for PEDOT devices under 1000 lux illumination.

EPFL2021