Increase In Conversion Efficiency Research Articles

A Facile Low Prevacuum Treatment to Enhance the Durability of Nonfullerene Organic Solar Cells

Herein, a straightforward vacuum‐assisted method is introduced to enhance the stability of nonfullerene organic solar cells (OSCs). The method, termed “prevacuum” involves subjecting the active layer (D18:Y6) to a low‐pressure vacuum (−1 bar) before thermal annealing at 100 °C. Compared to untreated devices, prevacuum‐treated OSCs exhibit a notable increase in power conversion efficiency from 13.71% to 14.90%. This enhancement is attributed to improved light absorption and charge extraction, as evidenced by external quantum efficiency measurements. Moreover, prevacuum treatment significantly improves device stability under operational conditions, with a 30% power loss occurring after 8.25 h compared to 4.5 h for untreated devices. This improvement is attributed to the removal of volatile components and impurities during the vacuum process, leading to a more hydrophobic and stable active layer. The study demonstrates the efficacy of prevacuum treatment as a simple and accessible method for enhancing the performance and longevity of OSCs, paving the way for their broader application in sustainable energy technologies.

Photovoltaic performance of pristine and arsenic doped hybrid perovskite

Under the scope of all-solid-state perovskite solar cells, the important role of methylammonium lead halide film lies in facilitating the formation of a photo-generated electronrich film, which directly affects the overall photovoltaic performance. This study introduces a novel chemical strategy aimed at increasing the quality of perovskite film through minimal arsenic doping. The result of the inclusion of arsenic is characterized by high crystalline grains in the attainment of a homogeneous, uniform and ancient perovskite film. The analysis of the UV-Visible spectra indicates that the perovskite film, which is produced under sequential conditions, displays light extraction of electrons for light absorption, more effective electron transport, and adjacent electron transport layer. Different morphology obtained through customized perovskite conditions contribute to a better short-circuits current, which improves overall cell performance. Arsenic-doped perovskite-based solar cells demonstrate a 1.55% increase in power conversion efficiency compared to their nondecorated counterparts, exhibiting 0.20% efficiency. The outcomes not only offer a straightforward method for enhancing perovskite films but also introduce an innovative perspective on constructing high-performance perovskite solar cells using minimal amounts of arsenic, thereby minimizing toxicity in the fabricated solar cells.

Nanoscale Graded Nitrogen-Doping of TiO2 via Pulsed Laser Deposition for Enhancing Charge Transfer in Perovskite Solar Cells.

An electron transport layer (ETL) for highly efficient perovskite solar cells (PSCs) should exhibit superior electrical transport properties and have its band levels aligned with interfacing layers to ensure efficient extraction of photo-generated carriers. Nitrogen-doped TiO2 (TiO2:N) is considered a promising ETL because it offers higher electrical conductivity compared to conventional ETLs made from spray-pyrolyzed TiO2. However, the application of highly doped TiO2:N in PSCs is often limited by the misalignment of energy band levels with adjacent layers and reduced optical transparency. In this study, a novel approach is introduced to enhance the charge transport characteristics and accurately align the electronic band alignment of TiO2:N layer through nanoscale doping level grading, achieved through the pulsed laser deposition (PLD) technique. The TiO2:N ETL with a graded doping profile can combine characteristics of both highly doped and lightly doped phases on each side. Furthermore, a nanoscale doping gradation, employing an ultrathin sub-layer structure with graded doping levels, creates a smoothly cascading band-level alignment that bridges the adjacent layers, enhancing the transport of photo-generated carriers. Consequently, this method leads to a substantial increase in the power conversion efficiency (PCE), exceeding 22%, which represents a relative improvement of 11% compared to traditional spray-pyrolyzed TiO2-based PSCs.

Enhanced‐Performance Electrodes from Biomass‐Derived Carbon (Rice Husk) for Printable Perovskite Solar Cells

In the quest for sustainable energy solutions, printable carbon‐based perovskite solar cells (p‐MPSCs) are capturing the industry's attention due to their exceptional stability, simplified assembly, and cost‐effectiveness. At the heart of this innovation lies the carbon electrode, favored for its straightforward printing and assembly processes, making it an ideal candidate for renewable photovoltaic applications that leverage biomass carbon. This study casts the spotlight on rice husks, a plentiful yet underutilized resource, repurposing them into carbon electrodes for p‐MPSCs through a specialized carbonization treatment. A comprehensive examination reveals that the integration of 20% rice husk carbon (RHC) with graphite significantly improves the material's filling and crystalline qualities, diminishes the density of defect states, and strengthens the suppression of nonradiative recombination. These advancements culminate in a notable increase in photovoltaic conversion efficiency, reaching up to 11.49%. This study not only demonstrates the viability of RHC in photovoltaic applications but also supports the efficient use of biomass carbon, contributing to the progression of green energy technologies.

Advancements in CIGS/ZnS heterojunction solar cells: Experimental and numerical analysis

This study presents a comprehensive experimental investigation conducted on a CIGS-based solar cell incorporating a ZnS buffer layer. The primary objective was to determine key parameters of the CIGS/ZnS heterojunction, including parasitic resistances (Rs and Rsh), ideality factor (n), and barrier height (ϕB), using experimental current-voltage (I-V) characteristics over a temperature range of 150 K to 300 K under dark conditions. The heterojunction was modelled using a single-diode electrical circuit that accounted for parasitic resistances. Two methods were employed for parameter determination: direct analysis of the (I-V) curves and Cheung's method. Additionally, the charge transport mechanism within the heterojunction is investigated and discussed. Furthermore, the performance of the Al:ZnO/i:ZnO/ZnS/CIGS/Mo solar cell was assessed using the SCAPS-1D simulator, demonstrating an initial solar energy conversion efficiency of 15.01 %. To enhance this efficiency, a hole transport layer (HTL) was integrated between the back electrode and the absorber layer. Extensive studies were conducted to optimize the thickness and doping density of the HTL, including a comparative analysis of different materials used as HTLs. These optimizations resulted in a significant increase in conversion efficiency, reaching up to 28.68 %.

Fabrication of PSCs with light absorption chips utilizing double-metal-cladding waveguide technology

Metal nanoparticles or periodic metal nanostructures exhibit localized surface plasmon resonance (LSPR) effects, widely employed in photovoltaic devices to enhance the light absorption. In this study, we used a double-metal-cladding waveguide (DMCW) structure to fabricate hexagonal metal nanostructures on the front side of the indium tin oxide (ITO) glass, positioned away from the incident light direction. We then prepared perovskite solar cells under various reaction conditions. The analysis results indicate that the metal nanostructure chip excites near-field coupling, generating strong localized fields, and enhances the light absorption through the LSPR effect. The perovskite solar cells (PSCs) with the chip structures exhibited a significant increase in short-circuit current density (JSC) and fill factor (FF), accompanied by a decrease in dark current, indicating improved photovoltaic characteristics of the cells. Altering the evaporative deposition time of the silver film and the concentration of the reaction solution led to a 12.79% increase in the power conversion efficiency (PCE) of the PSCs.

Enhancement and Predictable Guidance of Coalescence-Induced Droplet Jumping on V-Shaped Superhydrophobic Surfaces with a Ridge.

Coalescence-induced droplet jumping has attracted significant attention in recent years. However, achieving a high jumping velocity while predictably regulating the jumping direction of the merged droplets by simple superhydrophobic structures remains a challenge. In this work, a novel V-shaped superhydrophobic surface with a ridge is conceived for enhanced and predictably guided coalescence-induced droplet jumping. By conducting experiments and lattice Boltzmann simulations, it is found that the presence of a ridge in the V-shaped superhydrophobic surface can modify the fluid dynamics during the droplet coalescence process, resulting in a much higher droplet jumping velocity than that achieved by the V-shaped superhydrophobic surface without a ridge. The enhancement of the droplet jumping velocity is mainly attributed to the combined effect of the earlier and more sufficient impingement between the liquid bridge and the ridge, as well as the accelerated droplet contraction by redirecting the internal liquid flow toward the jumping direction. A high normalized jumping velocity of is achieved by the newly designed surface, with a 930% increase in the energy conversion efficiency in comparison with that on a flat surface. Moreover, adjusting the opening direction of the V-groove at different groove angles is found to be an effective method to regulate the droplet jumping direction and expand the range of the jumping angle. Particularly, the droplet jumping angle can be well predicted based on the rotational angle (ω) and the groove angle (α), i.e., θj,p ≈ 90° - 0.5α - ω.

Semiconductor heterojunctions coated with reduced graphite oxide as electron transfer materials for high-performance perovskite solar cells

Exploring and insight into the relationship between the microstructure, light absorption performance, and carrier transport of perovskite light absorption layer materials and carrier transport layer materials is crucial for obtaining efficient and stable perovskite solar cells. We adopted a simple strategy to prepare a composite material known as reduced graphene oxide wrapped mesoporous hierarchical TiO2–CdS semiconductor heterojunctions (TiO2–CdS-RGO) as the electron transport layer in formamidine lead iodide perovskite solar cells. Compared with single TiO2 and binary composite, this composite material exhibits enhanced photoluminescence quenching, reduced photo generated carrier recombination rate, and improved electron transfer capability. Photovoltaic devices based on TiO2–CdS-RGO composite material showed a 14.5 % increase in short-circuit current density (JSC) and a 36.3 % increase in photoelectric conversion efficiency (PCE) compared to those with only TiO2. The improved optoelectronic properties observed with the TiO2–CdS-RGO as electron transfer layers can be attributed to several factors. On the one hand, mesoporous TiO2 with a high specific surface area is beneficial for perovskite infiltration and enhances electron transfer rate. On the other hand, the well-matching energy level structure among the three components aids in electrons extraction and reduces the recombination rate of photo generated charge carriers; In addition, RGO nanosheets with high conductivity serve as an efficient electron transfer network, providing a rapid charge transfer pathways, which is crucial for enhancing the photoelectric conversion performance of perovskite solar cells.

Controlled solid‐state Phase Transition of Formamidinium Dominated Perovskite Layers Fabricated Through Magnetron Sputtering for Photovoltaics

AbstractPerovskite solar cells (PSCs) based on formamidinium lead iodide (FAPbI3) have demonstrated the highest power conversion efficiencies. Typically fabricated through solution‐processing, FAPbI3 films necessitate intricate crystallization control to avoid the formation of a more stable non‐perovskite phase. Magnetron sputtering, an effective solvent‐free technique, has gained attention for producing large‐area perovskite films. Here, a novel approach to create high‐quality FAPbI3‐based perovskite thin films by employing magnetron sputtering is presented. Specifically, a mechanosynthesized blend of (FA1‐xMAx)Pb(I1‐xBrx)3 (MA = methylammonium) is used as a single‐source target for sputtering, and a post‐annealing transforms various phases in the initial deposited film into coherent FAPbI3‐based films with an ultra‐long and controlled crystallization process. Despite minimal residual MABr after post‐annealing, its presence is crucial in the formation of perovskite film, as evidenced by a distinct solid‐state phase transformation process is presented. A comprehensive investigation of the films' structural, compositional, and optical properties, with respect to varying MABr doping ratios, reveals details of perovskite phase development and the pivotal influence of MABr. PSCs fabricated with the optimized films display a substantial increase in the power conversion efficiency, reaching 20.1%. These results underscore the potential of combining magnetron sputtering and post‐annealing in the scalable production of high‐efficiency PSCs.

Tungsten-Doped ZnO as an Electron Transport Layer for Perovskite Solar Cells: Enhancing Efficiency and Stability.

This study delves into enhancing the efficiency and stability of perovskite solar cells (PSCs) by optimizing the surface morphologies and optoelectronic properties of the electron transport layer (ETL) using tungsten (W) doping in zinc oxide (ZnO). Through a unique green synthesis process and spin-coating technique, W-doped ZnO films were prepared, exhibiting improved electrical conductivity and reduced interface defects between the ETL and perovskite layers, thus facilitating efficient electron transfer at the interface. High-quality PSCs with superior ETL demonstrated a substantial 30% increase in power conversion efficiency (PCE) compared to those employing pristine ZnO ETL. These solar cells retained over 70% of their initial PCE after 4000 h of moisture exposure, surpassing reference PSCs by 50% PCE over this period. Advanced numerical multiphysics solvers, employing finite-difference time-domain (FDTD) and finite element method (FEM) techniques, were utilized to elucidate the underlying optoelectrical characteristics of the PSCs, with simulated results corroborating experimental findings. The study concludes with a thorough discussion on charge transport and recombination mechanisms, providing insights into the enhanced performance and stability achieved through W-doped ZnO ETL optimization.

Enhancing photovoltaic panel efficiency with innovative cooling Technologies: An experimental approach

The increase in photovoltaic panel temperature brought on by solar radiation absorption lowers performance, power output, energy efficiency, and panel longevity (a rise in temperature of just one degree causes power drop of 0.41 %). In an effort to alleviate this problem, this thorough study multiple novel cooling strategies to enhance solar system efficiency, especially photovoltaic panels in Egyptian climates remote areas. The three main routines for photovoltaic panel cooling are contingent on the following techniques: (1) evaporative cooling using marble, (2) evaporative cooling using palm fibers with fan-assisted airflow, and (3) thermoelectric cooler modules. These materials that used in the studied system as coolants are characterized by, abundant local availability in nature and low cost, especially in Egypt. Every method has been designed with a control system. According to the study, starting the cooling process at the greatest temperature that is permitted—45 °C—produces the maximum energy output from photovoltaic panels while balancing the need for cooling and energy production. Using these cooling methods causes the average temperature to be lowered by 16, 11.62, and 9.8 degrees Celsius for thermoelectric, marble, and palm fiber cooling respectively while the voltage output is enhanced by 2.58, 0.94, and 0.7 V. The recorded values indicate 4.59 %, 3.95 %, 2.15 % increase in photovoltaic panel exit power and 25.29 %, 15.79 %, and 15.1 % increase in photovoltaic panel energy conversion efficiency when thermoelectric, marble, and palm fibers cooler modules are used, respectively. This study is a priceless resource for scholars looking to improve photovoltaic panel performance by executing efficient cooling strategies with annual costs 0.017, 0.02, 0.026, and 0.024 $/kWh and payback periods 1.69, 2.07, 2.71, and 2.48 years for reference panel, marble cooling panel, palm fiber cooling pane, and thermoelectric cooling panel respectively.

Butanol and selective catalytic reduction of gaseous emissions in a heavy-duty diesel engine

The impact of renewable fuels and their blends on vehicle exhaust emissions remains of high interest. In this study, we investigate the effect of butanol on the conversion efficiency of a Selective Catalytic Reduction (SCR) system installed on a commercial Euro V heavy-duty diesel engine (HDDE). Exhaust emissions were measured upstream and downstream of the SCR during dynamometer tests using diesel fuel and various butanol-diesel blends (5/95 %v, 10/90 %v, and 20/80 %v). Steady-state tests according to the World Harmonized Stationary Cycle (WHSC) on an engine bench were conducted including measurements of nitrogen oxides (NOX), total hydrocarbons (THC), and carbon monoxide (CO) emissions utilizing a portable emission measurement system (PEMS). The results showed a reduction in exhaust gas temperature (EGT) of around 4 % for a butanol content of 20 %. The use of butanol increased conversion efficiency of the SCR system by 4 % compared to diesel. The maximum SCR system conversion rate of around 96 % was obtained with a butanol content of 10 %. For all fuels, NOX conversion decreased at high engine loads (above 400 °C), while, as expected, was zero at low engine loads (below 200 °C). Reductions in CO and THC emissions were observed downstream of the SCR system. In general, this study shows that an SCR originally designed for a Euro V diesel engine can be equally effective when the engine is running on a partial blend of butanol.

A study of kapton as a flexible substrate for perovskite solar cells; advantages and disadvantages

The increasing usage of perovskite solar cells is being driven by their high efficiency and cost-effective manufacture. Polyethylene Terephthalate (PET) and Polyethylene Naphthalate (PEN) are flexible, transparent, and cost-effective. However, issues have been raised about their long-term stability, especially to the sensitivity of perovskite materials to environmental conditions like as moisture and heat, as well as the challenge of oxygen and moisture transmission across these substrates. Researchers are investigating Polyimide (PI), particularly colorless PI, for enhanced stability, but the techniques are costly. Kapton, a popular colored PI, provides excellent thermal and electrical insulation, but its reduced transparency provides optical issues. In this study, finite-difference-time-domain (FDTD) modeling and experimental analysis were utilized to investigate the optical properties and efficiency of perovskite solar cells on Kapton, PET, and glass substrates. According to the modeling, using Kapton instead of traditional substrates leads to a decrease of 16.6 % in the solar cells short circuit current (JSC). In laboratory experiments, by adding lithium (Li) as the dopant in the electron transport layer (ETL), the sheet resistance of the ETL was reduced from 214 to 2.4 kΩ/□. According to modeling, this enhancement resulted in a 3 % increase in the power conversion efficiency (PCE) of the solar cell, increasing to 17.4 % compared to 16.8 % on a PET substrate. Furthermore, using a Kapton substrate improves critical performance parameters like open circuit voltage (VOC) and fill factor (FF).

Effects on Metallization of n+-Poly-Si Layer for N-Type Tunnel Oxide Passivated Contact Solar Cells.

Thin polysilicon (poly-Si)-based passivating contacts can reduce parasitic absorption and the cost of n-TOPCon solar cells. Herein, n+-poly-Si layers with thicknesses of 30~100 nm were fabricated by low-pressure chemical vapor deposition (LPCVD) to create passivating contacts. We investigated the effect of n+-poly-Si layer thickness on the microstructure of the metallization contact formation, passivation, and electronic performance of n-TOPCon solar cells. The thickness of the poly-Si layer significantly affected the passivation of metallization-induced recombination under the metal contact (J0,metal) and the contact resistivity (ρc) of the cells. However, it had a minimal impact on the short-circuit current density (Jsc), which was primarily associated with corroded silver (Ag) at depths of the n+-poly-Si layer exceeding 40 nm. We introduced a thin n+-poly-Si layer with a thickness of 70 nm and a surface concentration of 5 × 1020 atoms/cm3. This layer can meet the requirements for low J0,metal and ρc values, leading to an increase in conversion efficiency of 25.65%. This optimized process of depositing a phosphorus-doped poly-Si layer can be commercially applied in photovoltaics to reduce processing times and lower costs.

Impact of Buried Interface Texture on Compositional Stratification and Ion Migration in Perovskite Solar Cells

AbstractDespite the striking increase in the power conversion efficiency (PCE) of lead‐based perovskite solar cells (PSCs), their poor operational stability impedes their commercialization. Among the various factors that influence device stability, ion migration has been identified as a key driver of degradation. In this work, the focus is on studying ion migration‐induced degradation in inverted architecture PSCs, which employ either a thin polymer layer or a self‐assembled monolayer (SAM) for hole extraction. It is demonstrated that the difference in texture imposed by the use of these hole transport layers (HTL) is an important and thus far inconspicuous factor that impacts ion migration, and consequently device stability. By investigating the buried interface in detail, it is revealed that its texture has a strong impact on the vertical compositional stratification in the perovskite active layer. By monitoring bias‐induced ion migration in devices with different hole extraction layers, it is demonstrated that the smooth polymer‐based HTL results in a higher degree of ion migration than the rough SAM HTL, corresponding to a stronger degradation in the former. These results further indicate that the use of SAMs for hole extraction is a promising strategy to suppress ion migration and improve device efficiency.

Comparative assessment of emissions, performance, and economics parameters for a dual–fuel diesel generator operating with rice bran biodiesel and hydrogen

The first step to achieving an energy transition is partially substituting fossil fuels with other more environmentally friendly alternatives, such as hydrogen gas. The current research aims to evaluate the influence of hydrogen in a diesel generator fueled with rice bran biodiesel. The above encourages the use of hydrogen and biodiesel production from residual raw material. For the development of the research, a diesel engine bench was used, which operated in five load conditions: 20 %, 40 %, 60 %, 80 %, and 100 %, and was fed with three fuels: −100 %, RB-10 %, and RB-10 % + H2(30 %). The results show that the mixture RB-10 % + H2(30 %) causes a 3.14 % reduction in BSFC and a 3.26 % increase in energy conversion efficiency. In addition, it is observed that a 9.90 %, 12.57 %, and 10.99 % decrease in HC, CO, and smoke opacity emissions compared to pure diesel. On the other hand, the mixture RB-10 % + H2(30 %) reduces by 4.44 %, 5.07 %, and 7.06 % the environmental, social, and ecological impact due to CO2, HC, and CO emissions, as well as a 3.93 % reduction in engine operating cost compared to RB-10 % biodiesel. In general, hydrogen injection is a promising alternative to promote the use of rice bran biodiesel due to its increased performance characteristics and reduced pollutant emissions without the need to modify the engine.

Lowering Charge Transport Barriers by Eliminating the Electric Double Layer Residues to Reconstruct Adjacent SnO2 Nanocrystals for High‐Efficiency Flexible Perovskite Solar Cells

AbstractThe sol–gel method is efficient and cost‐effective for synthesizing SnO2 sol, wherein SnO2 nanocrystallites (NCs) are stabilized by electric double‐layer of solvated ions tightly bound to their surface. However, this strong binding makes the removal of electric double‐layer residues from the SnO2 electron transport layer (ETL) to be difficult at low temperatures. This hinders both the close contact and subsequent growth among adjacent SnO2 NCs, leading to severe carriers scattering at grain boundary, adversely affecting the electrical properties of SnO2 ETL. Herein, SnO2 sol is synthesized via an ethanol‐based sol–gel method and aqueous ammonia (NH3·H2O) is introduced to effectively clean stubborn electric double‐layer residues within the SnO2 ETL at a low temperature (80 °C). Removing residues reduces the gap among adjacent SnO2 NCs and promotes further reconstructed growth through oriented attachment (OA), thereby reducing the number of grain boundaries. Hence, the energy barriers for electron transport decrease within the SnO2 ETL. Furthermore, MHP prepared on the treated ETL has fine‐tuned energy level alignment, improving the electron extraction capacity. Consequently, flexible perovskite solar cells (f‐PSCs) incorporating this ETL achieved a notable increase in power conversion efficiency, rising from 19.16% to 23.71%, as well as superior mechanical stability.

Gate-All-Around Nanopore Osmotic Power Generators.

Nanofluidic channels in a membrane represent a promising avenue for harnessing blue energy from salinity gradients, relying on permselectivity as a pivotal characteristic crucial for inducing electricity through diffusive ion transport. Surface charge emerges as a central player in the osmotic energy conversion process, emphasizing the critical significance of a judicious selection of membrane materials to achieve optimal ion permeability and selectivity within specific channel dimensions. Alternatively, here we report a field-effect approach for in situ manipulation of the ion selectivity in a nanopore. Application of voltage to a surround-gate electrode allows precise adjustment of the surface charge density at the pore wall. Leveraging the gating control, we demonstrate permselectivity turnover to enhanced cation selective transport in multipore membranes, resulting in a 6-fold increase in the energy conversion efficiency with a power density of 15 W/m2 under a salinity gradient. These findings not only advance our fundamental understanding of ion transport in nanochannels but also provide a scalable and efficient strategy for nanoporous membrane osmotic power generation.

Economical factitious diet for mass rearing of greater wax moth, Galleria mellonella (Lepidoptera: pyralidae), a promising host for entomopathogenic nematodes

BackgroundGreater wax moth (Galleria mellonella L.) (Lepidoptera: Pyralidae) is most commonly used for mass multiplication of entomopathogenic nematodes. An investigation on economical modification and comparative analysis of factitious diets of G. mellonella was carried out under laboratory conditions. Different diets were assessed in comparison with standard diet.ResultsModifications based on quantity change of dietary components (wheat flour, maize flour, dry milk, dry yeast, honey and glycerin), addition of vitamin E and vitamin-B complexes, elimination of dry milk and replacement of glycerin with sorbitol showed reduction in the cost of production and increase in food conversion efficiency in G. mellonella. The weight of larva in diet III (303.40 mg) was highest as compared to the larval weight in control diet (280.00mg). The conversion of ingested and digested food into biomass of G. mellonella was the highest for factitious diet III. Also, the highest number of Steinernema abbasi was produced from G. mellonella larvae reared on diet III (25418.43IJs) followed by diet I (21805.31IJs). The economics of the diets also showed that the percent cost reduction in factitious diet III and diet I was 48.86 and 28.85%, respectively. Overall, the results suggested that factitious diet III was superior to diet I followed by diet II.ConclusionAddition of supplements of vitamin E and B-complexes enhances the biological activity of the insect, thereby increasing its food conversion efficiencies. Factitious diet III can be successfully used for mass multiplication of the G. mellonella.

Unveiling the Role of BODIPY Dyes as Small‐Molecule Hole Transport Material in Inverted Planar Perovskite Solar Cells

Perovskite solar cells (PSCs) have become a research hotspot since their dramatic increase in power conversion efficiency (PCE), surpassing 26% due to advances in cell engineering and interfacial layers. Within the last factor, hole transporting materials play a crucial role in enhancing device performance and stability. Among several molecular building blocks, BODIPYs are attractive for the design of novel hole transporting material (HTMs) due to their outstanding photophysical and charge transport properties easily tuned by synthetic modifications. Herein, the synthesis of five new BODIPY‐based HTMs PyBDP 1–5 are reported, functionalized at the meso‐ and α‐ positions with pyrenyl and arylamino units, respectively. The resulting compounds exhibit broad absorption in the visible region, remarkable thermal stability, narrow bandgaps, suitable energy levels, and good hole extraction capability, as subtracted from experimental and computational characterizations. The performance of the BODIPY derivatives as HTMs is evaluated in planar inverted (p‐i‐n) PSCs and compared to commonly used PTAA, resulting in highly efficient systems, reaching PCEs very close to that obtained with the reference polymer (21.51%). The incorporation of these BODIPY‐based HTMs result in an outstanding PCE of 20.37% for devices including PyBDP‐1 and 19.97% for devises containing PyBDP‐3, thus demonstrating that BODIPY derivatives are a promising alternative to obtain simple and efficient organic HTMs.