Improved Charge Extraction Research Articles

Double-Side Improved Charge Extraction via 2D Perovskite for Efficient Inverted Perovskite Solar Cells

Double-Side Improved Charge Extraction via 2D Perovskite for Efficient Inverted Perovskite Solar Cells

Polymeric Charge-Transporting Materials for Inverted Perovskite Solar Cells.

Inverted perovskite solar cells (PSCs) hold exceptional promise as next-generation photovoltaic technology, where both perovskite absorbers and charge-transporting materials (CTMs) play critical roles in cell performance. In recent years, polymeric CTMs have played an important role in developing efficient, stable, and large-area inverted PSCs due to their unique properties of high conductivity, tunable structures, and mechanical flexibility. This review provides a comprehensive overview of polymeric CTMs used in inverted PSCs, encompassing polymeric hole transport materials (HTMs) and electron transport materials (ETMs). the relationship between their molecular structures, modification strategies are systematically summarized and analyzed for adjusting energy levels, and improving charge extraction, enabling a deep understanding of these widely used materials. The review also explores effective strategies for designing even more efficient polymeric CTMs. Finally, an outlook is proposed on the exciting research of novel polymeric CTMs, paving the way for their commercialized applications in PSCs.

Toward Commercial-Scale Perovskite Solar Cells: The Role of ALD-SnO2 Buffer Layers in Performance and Stability.

Hybrid organic-inorganic perovskite solar cells (PSCs) have shown significant potential in photovoltaic applications due to their superior optoelectronic properties. However, the conventional electron transport layer (ETL) of C60 in PSCs poses challenges such as incomplete coverage and metal diffusion, leading to reduced performance and stability. This work explores the efficacy of atomic layer deposition (ALD) of SnO2 as an interlayer between C60 and electrode to enhance the performance and stability of devices. Devices with varying SnO2 thicknesses were fabricated, revealing that a 15 nm ALD-SnO2 layer optimally improved the power conversion efficiency (PCE) to 23.85%, compared to the 22.86% achieved with a BCP layer. Moreover, the SnO2-based devices exhibited superior open-circuit voltage (VOC), short-circuit current density (JSC), and fill factor (FF). Modules (30 × 30 cm) with ALD-SnO2 demonstrated notable enhancements in efficiency and uniformity, suggesting the potential for scalable commercial applications. Photoluminescence (PL) and electrochemical impedance spectroscopy (EIS) analyses confirmed the improved charge extraction and reduced recombination with the SnO2 buffer layer. This research indicates that ALD-SnO2 is a promising interlayer candidate for PSCs, providing a pathway toward higher efficiency and stability in perovskite solar technology.

Reinforcing Photogenerated Carrier Extraction of Environment-Friendly InP/ZnSeS Quantum Dots for High-Performing Photoelectrochemical Photodetection and Solar Energy Conversion.

Colloidal InP/ZnSeS-based quantum dots (QDs) are considered promising building blocks for light-emitting devices due to their environmental friendliness, high quantum yield (QY), and narrow emission. However, the intrinsic type-I band structure severely hinders potential photoelectrochemical (PEC) applications requiring efficient photoexcited carrier separation and transfer. In this study, the optoelectronic properties of InP/ZnSeS QDs are tailored by introducing Al dopants in the ZnSeS layer, which concurrently passivate the surface defects and act as shallow donor states for suppressed non-radiative recombination and improved charge extraction efficiency. Consequently, as-fabricated InP/ZnSeS:Al QDs-based PEC-type photodetector exhibited a high detectivity up to 1011 Jones and a remarkable responsivity of 0.66 AW-1 at 600nm even under self-powered condition (0V bias). In addition, as-prepared InP/ZnSeS:Al QDs-based photoanode can be alternatively used for PEC hydrogen generation, showing an H2 production rate of 73.7µmol cm-2h-1 under 1 sun illumination (AM 1.5G, 100mW cm-2). The results offer a prospective strategy for optimizing eco-friendly QDs for high-performance multifunctional light detection/conversion devices.

Reducing Interfacial Recombination in Inverted Perovskite Solar Cells With Selenophene-Substituted PCBM: Comparison With Thiophene and Furan Substitution.

Reducing the interfacial recombination and improving the charge transfer capability of charge transport layers are effective strategies to enhance the efficiency and stability of perovskite solar cells (PSCs). This study evaluates, for the first time, the effects of selenophene substitution in the chemical structure of phenyl-butyric acid methyl ester (PCBM) on the performance and stability of inverted PSCs. Selenophene substitution was compared to thiophene and furan substitutions, and the reference PCBM without chalcogenophene moiety. Additionally, this study investigates the differences between using the fullerene cages C70 and C60 in the PCBM chemical structure. The photovoltaic results demonstrate that, with an adequate control of the thickness of the electron transport layer (ETL), incorporating the selenophene moiety in the structures of fullerenes enhances the photovoltaic parameters of PSCs. This improvement results from the reduction in trap-assisted recombination, an increase in electron mobility, and the improved charge extraction processes. The use of C70, as opposed to C60, allows for the preparation of a series of ETLs with comparable thicknesses, although slightly lower efficiencies. This feature facilitates a systematic comparative analysis focused on variations in the electron properties of ETLs, thereby avoiding the inclusion of issues related to thickness and charge recombination processes.

Magnetic Nanocomposite Modified Hybrid Hole-Transport Layer for Constructing Organic Solar Cells with High Efficiencies.

An interface modification layer holds paramount significance in reducing interface carrier recombination and improving the ohmic contact between the active layer and the electrode in organic solar cells (OSCs). Modifying or doping the widely used hole-transport layer (HTL) PEDOT:PSS to adjust the work function, conductivity, and acidity has become a common strategy for achieving high-performance OSCs. Metal oxides and two-dimensional materials as secondary dopants into PEDOT:PSS, respectively, as well as a replacement of PEDOT:PSS both exhibit immense potential for achieving high-performance OSCs due to their excellent electrical properties. Herein, we report a method utilizing a Fe3O4/GO magnetic nanocomposite as a secondary dopant for PEDOT:PSS to modulate its inherent properties for constructing high-efficiency OSCs. The magnetic nanocomposite hybrid HTL exhibits a suitable optical transmittance and higher work function. Meanwhile, it is found that the addition of Fe3O4/GO magnetic nanoparticles expands the domain of PEDOT and enhances the phase separation between PEDOT and PSS segments, thereby improving the conductivity of PEDOT:PSS. By fine-tuning the doping ratio of a Fe3O4/GO magnetic nanocomposite in PEDOT:PSS, the best power conversion efficiency of OSCs based on PM6:L8-BO was up to 18.91%. The notable enhancement of the device's performance was due to the enhanced hole mobility and the improved charge extraction, further complemented by the decreased likelihood of interface recombination brought about by the hybrid HTL. Compared with PEDOT:PSS-based OSCs, an enhanced stability of the hybrid HTL-based device was also obtained. In addition, the diverse adaptability of the hybrid HTL was demonstrated in enhancing the performance of OSCs that are based on PM6:Y6 and PBDB-T:ITIC. The effectiveness and versatility of a magnetic nanocomposite hybrid HTL present opportunities for achieving high-performance OSCs.

Tin-Lead Perovskite Solar Cells with Preferred Crystal Orientation by Buried Interface Approach.

Mixed tin-lead perovskite solar cells (PSCs) have garnered much attention for their ideal bandgap and high environmental research value. However, poly (3,4-ethylenedioxythiophene): poly (styrene sulfonate) (PEDOT: PSS), widely used as a hole transport layer (HTL) for Sn-Pb PSCs, results in unsatisfactory power conversion efficiency (PCE) and long-term stability of PSCs due to its acidity and moisture absorption. A synergistic strategy by incorporating histidine (HIS) into the PEDOT: PSS HTL is applied to simultaneously regulate the nucleation and crystallization of perovskite (PVK). HIS neutralizes the acidity of PEDOT: PSS and enhances conductivity. Especially, the coordination of the C═N and -COO- functional groups in the HIS molecule with Sn2+ and Pb2+ induces vertical growth of PVK film, resulting in the release of residual surface stress. Additionally, this strategy also optimizes the energy level alignment between the perovskite layer and the HTL, which improves charge extraction and transport. With these cooperative effects, the PCE of Sn-Pb PSCs reaches 21.46% (1 sun, AM1.5), maintaining excellent stability under a nitrogen atmosphere. Hence, the buried interface approach exhibits the potential for achieving high-performance and stable Sn-Pb PSCs.

Achieving 19.5% Efficiency via Modulating Electronic Properties of Peripheral Aryl-Substituted Small-Molecule Acceptors.

The advancement of acceptors plays a pivotal role in determining photovoltaic performance. While previous efforts have focused on optimizing acceptor-donor-acceptor1-donor-acceptor (A-DA1-D-A)-typed acceptors by adjusting side chains, end groups, and conjugated extension of the electron-deficient central A1 unit, the systematic exploration of the impact of peripheral aryl substitutions, particularly with different electron groups, on the A1 unit and its influence on device performance is still lacking. In this study, three novel acceptors - QxTh, QxPh, and QxPy - with distinct substitutions on the quinoxaline (Qx) are designed and synthesized. Density functional theory (DFT) analyses reveal that QxPh, featuring a phenyl-substituted Qx, exhibits the smallest molecular binding energies and a tightest π···π stacking distance. Consequently, the PM6:QxPh device demonstrates a better power conversion efficiency (PCE) of 17.1% compared to the blends incorporating QxTh (16.4%) and QxPy (15.7%). This enhancement is primarily attributed to suppressed charge recombination, improved charge extraction, and more favorable molecular stacking and morphology. Importantly, introducing QxPh as a guest acceptor into the PM6:BTP-eC9 binary system yields an outstanding PCE of 19.5%, indicating the substantial potential of QxPh in advancing ternary device performance. The work provides deep insights into the expansion of high-performance organic photovoltaic materials through peripheral aryl substitution strategy.

Enhancing efficiency and stability of perovskite solar cells with Bi2Te3 interlayer: insights from SCAPS simulation

Perovskite solar cells (PSCs) have gained much interest due to their high power conversion efficiencies (PCE). Affordable, accessible, and efficient solar energy is crucial for a sustainable and clean future. In this article, we optimized PSC efficiency and performance with an interlayer (IL) of Bi2Te3 (BT). Cell performance and efficiency were improved by incorporating BT IL with varied thicknesses. BT IL promotes electron transport while protecting the underlying structure from chemical instability, improving device performance. This simple and low-cost technology for producing efficient and stable all-inorganic PSC holds considerable potential as a next-generation renewable energy source. The main focus is optimizing all-inorganic PSC using Solar Cell Simulator Capacitance software (SCAPS). We systematically explore the influence of BT thickness and defect densities on the device performance. The impact of charge carrier transport and overall photovoltaic performance is studied. Our findings reveal that introducing the BT IL leads to improved charge extraction, reduced recombination losses, and enhanced stability in the PSC. The optimized device configuration significantly enhances PCE compared to reference devices without BT IL. This study provides valuable insights into the potential use of BT ILs as a strategy to boost the efficiency and stability of PSCs.

Chlorine-Substituent Regulation in Dopant-Free Small-Molecule Hole-Transport Materials Improves the Efficiency and Stability of Inverted Perovskite Solar Cells

Although doped hole-transport materials (HTMs) offer an efficiency benefit for perovskite solar cells (PSCs), they inevitably diminish the stability. Here, we describe the use of various chlorinated small molecules, specifically fluorenone-triphenylamine (FO-TPA)-x-Cl [x = para, meta, and ortho (p, m, and o)], with different chlorine-substituent positions, as dopant-free HTMs for PSCs. These chlorinated molecules feature a symmetrical donor–acceptor–donor structure and ideal intramolecular charge transfer properties, allowing for self-doping and the establishment of built-in potentials for improving charge extraction. Highly efficient hole-transfer interfaces are constructed between perovskites and these HTMs by strategically modifying the chlorine substitution. Thus, the chlorinated HTM-derived inverted PSCs exhibited superior efficiencies and air stabilities. Importantly, the dopant-free HTM FO-TPA-o-Cl not only attains a power conversion efficiency of 20.82% but also demonstrates exceptional stability, retaining 93.8% of its initial efficiency even after a 30-day aging test conducted under ambient air conditions in PSCs without encapsulation. These findings underscore the critical role of chlorine-substituent regulation in HTMs in ensuring the formation and maintenance of efficient and stable PSCs.

Ni-NCDs promoted photocatalytic benzylamine oxidation coupled hydrogen production in Cu-In-Zn-S/WO3·H2O Z-scheme heterojunction

The construction of Z-scheme heterojunction is important for efficient photocatalytic organic oxidation coupled hydrogen production. However, current methods suffer from poor synergy of charge extraction and surface reactions. In this study, we combined Cu-In-Zn-S (CIZS) quantum dots with WO3·H2O (WO) nanosheets to form a Z-scheme heterojunction, which was further modified with bifunctional N-doped carbon dots (NCDs) to improve charge extraction and abundant Ni sites for hydrogen evolution. The unique 0D/2D/0D CIZS/WO/Ni-NCDs heterojunction resulted in a hydrogen production rate of 4.261 mmol g−1 h−1, with ascorbic acid, 8.06 times higher than that of CIZS. In addition, the selectivity of N-benzylidenebenzylamine from benzylamine oxidation reaction has been increased from 31.65 % to 73.34 %. This improvement can be attributed to the efficient charge separation, transfer, and surface reactions accelerated by the multifunctional Ni-NCDs. A series of photoelectrochemical tests and radical scavenging experiments confirmed the Z-scheme photocatalytic process and the important roles of superoxide radicals and holes. Photo-induced electrocatalysis tests further confirmed the accelerated hydrogen evolution reaction in the presence of Ni-NCDs. Furthermore, time-resolved photoluminescence test demonstrated that the synergies of NCDs and Ni significantly extended the charge carrier lifetime. These findings provide valuable insights into efficient hydrogen production through the modulation of Z-scheme heterojunctions using bifunctional metal-carbon dots.

Interface Dipole Management of D–A‐Type Molecules for Efficient Perovskite Solar Cells

AbstractInterfacial engineering of perovskite films has been the main strategies in improving the efficiency and stability of perovskite solar cells (PSCs). In this study, three new donor‐acceptor (D–A)‐type interfacial dipole (DAID) molecules with hole‐transporting and different anchoring units are designed and employed in PSCs. The formation of interface dipoles by the DAID molecules on the perovskite film can efficiently modulate the energy level alignment, improve charge extraction, and reduce non‐radiative recombination. Among the three DAID molecules, TPA‐BAM with amide group exhibits the best chemical and optoelectrical properties, achieving a champion PCE of 25.29 % with the enhanced open‐circuit voltage of 1.174 V and fill factor of 84.34 %, due to the reduced defect density and improved interfacial hole extraction. Meanwhile, the operational stability of the unencapsulated device has been significantly improved. Our study provides a prospect for rationalized screening of interfacial dipole materials for efficient and stable PSCs.

Interface Dipole Management of D-A-Type Molecules for Efficient Perovskite Solar Cells.

Interfacial engineering of perovskite films has been the main strategies in improving the efficiency and stability of perovskite solar cells (PSCs). In this study, three new donor-acceptor (D-A)-type interfacial dipole (DAID) molecules with hole-transporting and different anchoring units are designed and employed in PSCs. The formation of interface dipoles by the DAID molecules on the perovskite film can efficiently modulate the energy level alignment, improve charge extraction, and reduce non-radiative recombination. Among the three DAID molecules, TPA-BAM with amide group exhibits the best chemical and optoelectrical properties, achieving a champion PCE of 25.29 % with the enhanced open-circuit voltage of 1.174 V and fill factor of 84.34 %, due to the reduced defect density and improved interfacial hole extraction. Meanwhile, the operational stability of the unencapsulated device has been significantly improved. Our study provides a prospect for rationalized screening of interfacial dipole materials for efficient and stable PSCs.

Modification of hydrophobic PTAA layer with Al2O3 nanoparticle over large-area inverted perovskite solar cell

Poly (triaryl amine) [PTAA] has been used as a promising hole-transport layer (HTL) for the p-i-n device architecture to fabricate high-efficiency perovskite solar cells (PSCs). Further improvement of perovskite device stability and efficiency is essential to make them commercially viable. In the present work, incorporating Al2O3-nanoparticles (NPs) at the PTAA/Perovskite interface exhibits enhanced surface coverage and reduced surface roughness, facilitating improved charge extraction and reduced charge recombination. The PTAA layer passivated with 2.0 wt% Al2O3-Nanoparticles (NPs) boosted the PCE of the PSCs from 11.11 % to 14.72 % (0.25 cm2 cell) and from 7.2 % to 9.2 % (2.0 cm2 cell), respectively. Moreover, the devices maintained 79 % and 74 % PCE of their initial efficiency values after 2000 h of storage in ambient conditions.

Fabrication of Efficient and Simple-Structured Perovskite Solar Cells Using a Multifunctional Biocolina Surface Treatment.

The electron transport layer (ETL)-free perovskite solar cells (PSCs) have gained significant interest by simplifying the manufacture process and reducing the time/energy required for the fabrication of ETLs. Unfortunately, the performance of these ETL-free PSCs still lags behind those of the conventional counterparts due to the slow electron extraction and undesired interfacial charge recombination loss at the buried interface. In this work, a facile and multifunctional biocolina thin layer is incorporated on the bottom electrodes to regulate the interface energy level alignment by forming an interface dipole layer, resulting in a suppressed nonradiative recombination and an improved charge extraction. Furthermore, the biocolina thin layer possess the capability to passivate the surface defects within the perovskite films while simultaneously facilitate the formation of perovskite crystals. Consequently, a remarkable enhancement in photovoltaic performance is observed in the biocolina-based ETL-free PSCs with an increase from 15.96 % to an outstanding 20.01 %. Additionally, the biocolina extends the stability and relieves the hysteresis effect through the interface defect passivation and inhibition of interface charge accumulation. This research contributes to the development of cost-effective, simplified designs for highly efficient ETL-free PSCs by modifying the bottom electrodes.

Improving Thermal Stability of High-Efficiency Methylammonium-Free Perovskite Solar Cells via Chloride Additive Engineering.

Tin dioxide (SnO2), in perovskite solar cells (PSCs), stands out as the material most suited to the electron transport layer (ETL), yielding advantages with regard to ease of preparation, high mobility, and favorable energy level alignment. Nonetheless, there is a chance that energy losses from defects in the SnO2 and interface will result in a reduction in the Voc. Consequently, optimizing the interfaces within solar cell devices is a key to augmenting both the efficiency and the stability of PSCs. Herein this present study, we introduced butylammonium chloride (BACl) into the SnO2 ETL. The resulting optimized SnO2 film mitigated interface defect density, thereby improving charge extraction. The robust bonding capability of negatively charged Cl- ions facilitated their binding with noncoordinated Sn4+ ions, effectively passivating defects associated with oxygen vacancies and enhancing charge transport within the SnO2 ETL. Concurrently, doped BA+ and Cl- diffused into the perovskite lattice, fostering perovskite grain growth and reducing the defects in perovskite. In comparison to the control device, the Voc saw a 70 mV increase, achieving a champion efficiency of 22.86%. Additionally, following 1000 h of ambient storage, the unencapsulated device based on SnO2 preburied with BACl retained around 90% of its initial photovoltaic conversion efficiency.

Recent Advances in Carbon Nanotube Utilization in Perovskite Solar Cells: A Review.

Due to their exceptional optoelectronic properties, halide perovskites have emerged as prominent materials for the light-absorbing layer in various optoelectronic devices. However, to increase device performance for wider adoption, it is essential to find innovative solutions. One promising solution is incorporating carbon nanotubes (CNTs), which have shown remarkable versatility and efficacy. In these devices, CNTs serve multiple functions, including providing conducting substrates and electrodes and improving charge extraction and transport. The next iteration of photovoltaic devices, metal halide perovskite solar cells (PSCs), holds immense promise. Despite significant progress, achieving optimal efficiency, stability, and affordability simultaneously remains a challenge, and overcoming these obstacles requires the development of novel materials known as CNTs, which, owing to their remarkable electrical, optical, and mechanical properties, have garnered considerable attention as potential materials for highly efficient PSCs. Incorporating CNTs into perovskite solar cells offers versatility, enabling improvements in device performance and longevity while catering to diverse applications. This article provides an in-depth exploration of recent advancements in carbon nanotube technology and its integration into perovskite solar cells, serving as transparent conductive electrodes, charge transporters, interlayers, hole-transporting materials, and back electrodes. Additionally, we highlighted key challenges and offered insights for future enhancements in perovskite solar cells leveraging CNTs.

Improved charge extraction in inverted perovskite solar cells with dual-site-binding ligands.

Inverted (pin) perovskite solar cells (PSCs) afford improved operating stability in comparison to their nip counterparts but have lagged in power conversion efficiency (PCE). The energetic losses responsible for this PCE deficit in pin PSCs occur primarily at the interfaces between the perovskite and the charge-transport layers. Additive and surface treatments that use passivating ligands usually bind to a single active binding site: This dense packing of electrically resistive passivants perpendicular to the surface may limit the fill factor in pin PSCs. We identified ligands that bind two neighboring lead(II) ion (Pb2+) defect sites in a planar ligand orientation on the perovskite. We fabricated pin PSCs and report a certified quasi-steady state PCE of 26.15 and 24.74% for 0.05- and 1.04-square centimeter illuminated areas, respectively. The devices retain 95% of their initial PCE after 1200 hours of continuous 1 sun maximum power point operation at 65°C.

Interface engineering and defect passivation for enhanced hole extraction, ion migration, and optimal charge dynamics in both lead-based and lead-free perovskite solar cells

The study elucidates the potential benefits of incorporating a BiI3 interfacial layer into perovskite solar cells (PSCs). Using MAPbI3 and MAGeI3 as active layers, complemented by the robust TiO2 and Spiro-OMeTAD as the charge-transport-layers, we employed the SCAPS-1D simulation tool for our investigations. Remarkably, the introduction of the BiI3 layer at the perovskite-HTL interface significantly enhanced hole extraction and effectively passivated defects. This approach minimized charge recombination and ion migration towards opposite electrodes, thus elevating device performance relative to conventional configurations. The efficiency witnessed a rise from 19.28 to 20.30% for MAPbI3 and from 11.90 to 15.57% for MAGeI3. Additionally, MAGeI3 based PSCs saw an improved fill-factor from 50.36 to 62.85%, and a better Jsc from 13.22 to 14.2 mA/cm2, signifying reduced recombination and improved charge extraction. The FF for MAPbI3 based PSCs saw a minor decline, while the Voc slightly ascended from 1.24 to 1.25 V and Jsc from 20.01 to 21.6 mA/cm2. A thorough evaluation of layer thickness, doping, and temperature further highlighted the critical role of the BiI3 layer for both perovskite variants. Our examination of bandgap alignments in devices with the BiI3 interfacial layer also offers valuable understanding into the mechanisms fueling the observed improvements.

Fluorinated organic ammonium salt passivation for high-efficiency and stable inverted CsPbI2Br perovskite solar cells.

All-inorganic CsPbI2Br inverted perovskite solar cells (PSCs) have drawn increasing attention because of their outstanding thermal stability and compatible process with tandem cells. However, relatively low open circuit voltage (Voc) has lagged their progress far behind theoretical limits. Herein, we introduce phenylmethylammonium iodide and 4-trifluoromethyl phenylmethylammonium iodide (CFPMAI) on the surface of a CsPbI2Br perovskite film and investigate their passivation effects. It is found that CFPMAI with a -CF3 substituent significantly decreases the trap density of the perovskite film by forming interactions with the under-coordinated Pb2+ ions and effectively suppresses the non-radiative recombination in the resulting PSC. In addition, CFPMAI surface passivation facilitates the optimization of energy-level alignment at the CsPbI2Br perovskite/[6,6]-phenyl C61 butyric acid methyl ester interface, resulting in improved charge extraction from the perovskite to the charge transport layer. Consequently, the optimized inverted CsPbI2Br device exhibits a markedly improved champion efficiency of 14.43% with a Voc of 1.12V, a Jsc of 16.31 mA/cm2, and a fill factor of 79.02%, compared to the 10.92% (Voc of 0.95V) efficiency of the control device. This study confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement.