Power Conversion Efficiency Research Articles

Enhanced Performance and Stability of CsPbBr3 Perovskite Solar Cells Using Trioctylphosphine Oxide Additive.

This study investigates the application of trioctylphosphine oxide (TOPO) and triphenylphosphine oxide (TPPO) as an additive to enhance the performance of all-inorganic CsPbBr3 perovskite solar cells (PSCs). The addition of TOPO and TPPO passivates surface defects, increases grain size, and reduces surface trap states, leading to better light absorption and accelerated carrier transport. These modifications lead to an optimized energy level distribution, resulting in a significant increase in power conversion efficiency from 5.14 to 9.21% with TOPO and from 5.14% to 7.28% with TPPO. Furthermore, the long alkyl chains in TOPO provide effective isolation from air and water, significantly enhancing device stability for over 2400 h without packaging. The findings demonstrate that oxygen phosphine additives with long alkane chains are more effective in improving PSCs than those with aromatic hydrocarbons, offering new insights for the use of passivators in perovskite solar cells.

High Efficiency (>10%) AgBiS2 Colloidal Nanocrystal Solar Cells with Diketopyrrolopyrrole-Based Polymer Hole Transport Layer.

Silver bismuth disulfide (AgBiS2) colloidal nanocrystals (CNCs) have emerged as ecofriendly photoactive materials with excellent photoconductivity and high absorption coefficients, in compliance with the restriction of hazardous substances (RoHS) guidelines. To maximize the theoretical potential of AgBiS2 CNC solar cells, a new diketopyrrolopyrrole (DPP)-based polymer, BD2FCT, optimized as a hole transport layer (HTL), is developed. This asymmetric thiophene-rich polymer HTL effectively complements the optical absorption spectrum of CNCs and forms a homogeneous layer atop the CNCs, facilitating favorable vertical charge transfer through intrinsic molecular packing. Furthermore, the BD2FCT HTL aligns energetically with AgBiS2, significantly reducing charge recombination at the CNC/HTL interfaces and enhancing charge extraction and photocurrent generation across the entire optical absorption spectrum. These characteristics are further optimized through precise molecular engineering. Additionally, a low-bandgap acceptor, IEICO-4F, is structurally incorporated with the BD2FCT polymer to further improve charge funneling and complementary absorption. Transient absorption spectroscopy reveals enhanced hole transfer from CNC to BD2FCT-29DPP:IEICO-4F, resulting in reduced charge recombination and efficient charge extraction. Consequently, a BD2FCT-based AgBiS2 CNC solar cell achieves a power conversion efficiency (PCE) of 10.1%, demonstrating significant improvements in short-circuit current density (JSC) and fill factor (FF).

Chloride Engineering for Boosting Perovskite Photovoltaics: Impact on Precursor Coordination, Crystallization, and Film Quality.

Perovskite solar cells (PSCs) have seen rapid advancements over the past decade, driven by their exceptional optoelectronic properties and high power conversion efficiencies. Cl-based additives strategy has significantly contributed to these advancements by enhancing crystallinity, improving preferred orientation, and optimizing the surface morphology of perovskite films. This review provides a comprehensive summary of recent advancements and insights into the critical role of Cl-based additives in perovskite photovoltaics, focusing on the mechanisms behind Cl incorporation and its effects on film and device performance. First, the impact of Cl on precursor solution coordination and colloidal characteristics is discussed. Then, how Cl-based additives influence the phase transitions of perovskites, including methylammonium lead iodide (MAPbI3), formamidinium lead iodide (FAPbI3), and 2D perovskites is examined. Furthermore, the impact of Cl-based interfacial treatments on perovskite film quality is explored. Based on these insights, the overall impact of Cl treatments is also reviewed on the properties of perovskite films. Finally, a brief overview of the remaining challenges and future perspectives are provided to guide ongoing research efforts toward optimizing Cl additive engineering for high-performance PSCs.

Suppressing Exciton-Vibration Coupling via Intramolecular Noncovalent Interactions for Low-Energy-Loss Organic Solar Cells.

Minimizing energy loss is crucial for breaking through the efficiency bottleneck of organic solar cells (OSCs). The main mechanism of energy loss can be attributed to non-radiative recombination energy loss (ΔEnr) that occurs due to exciton-vibration coupling. To tackle this challenge, tuning intramolecular noncovalent interactions is strategically utilized to tailor novel fused ring electron acceptors (FREAs). Upon comprehensive analysis of both theoretical and experimental results, this approach can effectively enhance molecular rigidity, suppress structural relaxation, reduce exciton reorganization energy, and weakens exciton-vibration coupling strength. Consequently, the binary OSC device based on Y-SeSe, which features dual strong intramolecular Se···O noncovalent interactions, achieves an outstanding power conversion efficiency (PCE) of 19.49%, accompanied by an extremely small ΔEnr of 0.184 eV, much lower than those of Y-SS and Y-SSe based devices with weaker intramolecular noncovalent interactions. These achievements not only set an efficiency record for selenium-containing OSCs, but also mark the lowest reported ΔEnr value among high-performance binary devices. Furthermore, the ternary blend device showcases a remarkable PCE of 20.51%, one of the highest PCEs for single-junction OSCs. This work demonstrates the effectiveness of intramolecular noncovalent interactions in suppressing exciton-vibration coupling, thereby achieving low-energy-loss and high-efficiency OSCs.

Design and simulation of CsPb.625Zn.375IBr2-based perovskite solar cells with different charge transport layers for efficiency enhancement

In this work, CsPb.625Zn.375IBr2-based perovskite solar cells (PSCs) are numerically simulated and optimized under ideal lighting conditions using the SCAPS-1D simulator. We investigate how various hole transport layers (HTL) including Zn3P2, PTAA, MoS2, MoO3, MEH-PPV, GaAs, CuAlO2, Cu2Te, ZnTe, MoTe2, CMTS, CNTS, CZTS, CZTSe and electron transport layers (ETL) such as CdS, SnS2, ZnSe, PC60BM interact with the devices’ functionality. Following HTL material optimization, a maximum power conversion efficiency (PCE) of 16.59% was observed for the FTO/SnS2/CsPb.625Zn.375IBr2/MoS2/Au structure, with MoS2 proving to be a more economical option. The remainder of the investigation is done following the HTL optimization. We study how the performance of the PSC is affected by varying the materials of the ETL and to improve the PCE of the device, we finally optimized the thickness, charge carrier densities, and defect densities of the absorber, ETL, and HTL. In the end, the optimized arrangement produced a VOC of 0.583 V, a JSC of 43.95 mA/cm2, an FF of 82.17%, and a PCE of 21.05% for the FTO/ZnSe/CsPb.625Zn.375IBr2/MoS2/Au structure. We also examine the effects of temperature, shunt resistance, series resistance, generation rate, recombination rate, current-voltage (JV) curve, and quantum efficiency (QE) properties to learn more about the performance of the optimized device. At 300 K, the optimized device provides the highest thermal stability. Our research shows the promise of CsPb.625Zn.375IBr2-based PSCs and offers insightful information for further development and improvement.

Highly accurate, efficient, and fabrication tolerance-aware nanostructure prediction for high-performance optoelectronic devices

Despite extensive efforts to predict optimal nanostructures for enhancing optical devices, a more accurate, efficient, and practical method for nanostructure optimisation is required. In particular, fabrication tolerance is a promising avenue for significantly improving manufacturing efficiency; however, research in this area is limited. In this study, we introduce a practical approach for enhancing the performance of optoelectronic devices using an artificial intelligence (AI)-based nanostructure optimisation strategy. We optimised a support vector regression (SVR) model to capture the complex and nonlinear relationships between the transmittance and nanograting structure variables with the goal of improving optoelectronic devices. Our versatile model accurately predicted the continuous transmittance data with high precision (R2 = 0.995) using only 216 training data points. It can also make predictions under untrained conditions, thereby enabling the creation of a transmittance nanostructure contour map (R2 = 0.949). This method facilitates the design of nanostructures tailored to specific optical properties and provides valuable insights into fabrication tolerance. Through experimental validation, we identified an optimal nanograting structure with the highest transmittance in the visible-light spectrum. When integrated into optoelectronic devices such as organic light-emitting diodes (OLEDs) and organic solar cells (OSCs), their performance is significantly improved by increasing the light transmittance. Specifically, devices using the fabricated nanograting film exhibited a 17% improvement in external quantum efficiency (EQE) for solution-processed organic light-emitting diodes (SP-OLEDs) and a 10.7% improvement in power-conversion efficiency (PCE) for OSCs.

Helical π‐Extended Terrylene Diimide Dimer Based on Ring‐Fused Ethylene Bridge for Organic Solar Cells

AbstractTerrylene diimides (TDIs), as the higher homologues of perylene diimide (PDI) in the series of rylene diimides (RDIs), exhibit several especial properties including enhanced absorption ability in the near infrared (NIR) region, higher fluorescence quantum yields as well as stronger π–π stacking in comparison to naphthalene diimides (NDIs) and perylene diimides (PDIs). However, TDIs have been largely overlooked in terms of their photovoltaic applications because of the chemical inaccessibility and poor solubility. In this contribution, a helical π‐extended terrylene diimide dimer based on ring‐fused ethylene bridge, namely FTDI2 is designed and synthesized. The photovoltaic performances of FTDI2 and the parent TDI are investigated using the commercially available PTB7‐Th as the electron donor. A significantly improved power‐conversion efficiency (PCE) of 5.11 % compared to that of TDI based ones (0.5 %) is achieved for FTDI2‐based device, demonstrating the potential of terrylene dyes in the photovoltaics field.

Enhancing Flexibility, Long-Term Stability, and Efficiency in Full Air Fabricated Perovskite Solar Cells via Multifunctional Fluorinated Polyurethane Additives.

Perovskite films often suffer from surface and grain boundary defects, including uncoordinated ions, lattice distortions, and dangling bonds, coupled with lattice distortions due to solvent volatilization anisotropy and the thermal expansion coefficient. Such defects severely compromise both the photovoltaic efficiency and long-term solar cell stability. Here, fluorinated polyurethane (FPU) was synthesized and introduced into the perovskite precursor as a multifunctional additive. Excess Pb2+ ions interact with the carbonyl group (C═O) of FPU, thereby reducing nonradiative recombination. The perovskite and FPU form various hydrogen bonds via MA+ with F and -NH with -I. This multiplies the passivation of grain boundary defects, increases grain size, reduces defect density, releases residual lattice stress, and facilitates charge transport. Accordingly, the power conversion efficiency of the FPU-modified perovskite solar cells (PSCs) on rigid substrates and flexible substrates reached 21.18 and 17.76%, respectively. Notably, the long-chain C-F compound, which constructs a moisture-resistant barrier, could inhibit moisture corrosion in the perovskite films. After 2000 h of storage at ambient temperature in dark, the PSCs's initial efficiency still remained 82%. Additionally, after it undergoes 300 bending cycles (r = 0.7 cm), the device maintains 92.4% of its initial efficiency.

Methylthio Substituent in SAM Constructing Regulatory Bridge with Photovoltaic Perovskites

Inverted (p‐i‐n) perovskite solar cells (PSCs) have experienced remarkable advancements in recent years, which is largely attributed to the development of novel hole‐transport layer (HTL) self‐assembled monolayer (SAM) materials. Methoxy (MeO‐) groups are typically introduced into SAM materials to enhance their wettability and effectively passivate the perovskite buried interface. However, MeO‐based SAM materials exhibit a mismatch in highest occupied molecular orbital (HOMO) levels with perovskite layer due to the strong electron‐donating capability of methoxy group. In this work, we introduced a methylthio (MeS‐) substituent that is superior to methoxy as a highly versatile self‐assembled molecular design strategy. As a soft base, sulfur atom forms a stronger Pb‐S bond than oxygen. Additionally, within the CbzPh series of SAM materials, MeS‐CbzPh demonstrates a more optimal HOMO level and enhanced hole transport properties. Consequently, the MeS‐CbzPh HTL based device achieved an impressive power conversion efficiency (PCE) of 26.01% and demonstrated high stability, retaining 93.3% efficiency after 1000 hours of maximum power point tracking (MPPT). Moreover, in comparison with the commonly used 4PACz‐based SAM molecular series, MeS‐4PACz also exhibited the best performance among its peers. Our work provides valuable insights for the molecular design of SAM materials, offering a highly versatile functional substituent group.

Methylthio Substituent in SAM Constructing Regulatory Bridge with Photovoltaic Perovskites

Inverted (p‐i‐n) perovskite solar cells (PSCs) have experienced remarkable advancements in recent years, which is largely attributed to the development of novel hole‐transport layer (HTL) self‐assembled monolayer (SAM) materials. Methoxy (MeO‐) groups are typically introduced into SAM materials to enhance their wettability and effectively passivate the perovskite buried interface. However, MeO‐based SAM materials exhibit a mismatch in highest occupied molecular orbital (HOMO) levels with perovskite layer due to the strong electron‐donating capability of methoxy group. In this work, we introduced a methylthio (MeS‐) substituent that is superior to methoxy as a highly versatile self‐assembled molecular design strategy. As a soft base, sulfur atom forms a stronger Pb‐S bond than oxygen. Additionally, within the CbzPh series of SAM materials, MeS‐CbzPh demonstrates a more optimal HOMO level and enhanced hole transport properties. Consequently, the MeS‐CbzPh HTL based device achieved an impressive power conversion efficiency (PCE) of 26.01% and demonstrated high stability, retaining 93.3% efficiency after 1000 hours of maximum power point tracking (MPPT). Moreover, in comparison with the commonly used 4PACz‐based SAM molecular series, MeS‐4PACz also exhibited the best performance among its peers. Our work provides valuable insights for the molecular design of SAM materials, offering a highly versatile functional substituent group.

Tuning of the Polymeric Nanofibril Geometry via Side-Chain Interaction toward 20.1% Efficiency of Organic Solar Cells.

Constructing fibril morphology has been believed to be an effective method of achieving efficient exciton dissociation and charge transport in organic solar cells (OSCs). Despite emerging endeavors on the fibrillization of organic semiconductors via chemical structural design or physical manipulation, tuning of the fibril geometry, i.e., width and length, for tailored optoelectronic properties remains to be studied in depth. In this work, a series of alkoxythiophene additives featuring varied alkyl side chains connected to thiophene are designed to modulate the growth of fibril aggregates in cutting-edge polymer donors PM6 and D18. Molecular dynamics simulations and morphological characterizations reveal that these additives preferentially locate near and entangle with the side chains of polymer donors, which enhance the conjugated backbone stacking of polymer donors to form nanofibrils with the width expanding from 12.6 to 21.8 nm and the length increasing from 98.3 to 232.7 nm. This nanofibril structure is feasible to acquire efficient exciton dissociation and charge transport simultaneously. By integrating the fibril PM6 and L8-BO as the donor and acceptor layers in pseudo-bulk heterojunction (p-BHJ) OSCs via layer-by-layer deposition, an improvement of power conversion efficiency (PCE) from 18.7% to 19.8% is observed, contributed by enhanced light absorption, charge transport, and reduced charge recombination. The versatility of these additives is also verified in D18:L8-BO OSCs, with enhanced PCE from 19.3% to 20.1%, which is among the highest values reported for OSCs.

Effect of PANI-Doped-Graphene Oxide as HTL in Perovskite Solar Cells Using SCAPS-1D Software

This research examines and analyses the solar cell performance of methylammonium lead triiodide (MAPbI3) perovskite solar cells (PSC) that utilize Polyaniline (PANI)-doped-graphene oxide (GO) as HTL. Additionally, the study used the SCAPS-1D simulation software to model and analyze the experimental data. The simulated data generated by the SCAPS-1D software is afterward compared to the experimental findings. This comparison serves as a foundation for further optimization of the solar cell's performance. This study explicitly examined the impact of layer thickness and doping density on device performance in order to determine which parameters should be optimized to enhance overall performance. The SCAPS-1D simulation obtained a highest power conversion efficiency (PCE) of 15.37%. This work presented an improved efficiency of 40% from the experimental data. The findings of our study have the potential to be used in the prediction of key parameters for the optimization of perovskite solar cells (PSCs) using doped PANI/GO as a hole transport layer (HTL).

Enhancing the Performance of Perovskite Solar Cells by Extending the Terminal Conjugation of Spiro‐Type Hole Transport Material

Hole transport materials (HTM) play a vital role in the performance of perovskite solar cells (PSCs). Optimizing the molecular structure of HTMs has been proven to be an important method for improving PSCs’ efficiency and stability. Herein, a novel dibenzofuran‐terminated spiro‐type HTM with extending π‐conjugation is designed and developed, named spiro‐BNF. The structure–property relationship is also studied with spiro‐OMeTAD and spiro‐DBF as the reference. The results show that spiro‐BNF has improved hole mobility and glass transition temperature (reaching 198 °C) than spiro‐OMeTAD and spiro‐BDF. spiro‐BNF also exhibits matched highest occupied molecular orbital level with perovskite and superior morphology on the perovskite layer. Accordingly, the PSCs employing spiro‐BNF display a higher power conversion efficiency of 23.65% and improved stability than the device employing spiro‐OMeTAD or spiro‐BDF. The findings provide a new insight for enhancing the performance of PSCs.

Enhanced photovoltaic performance and longevity of perovskite modules via interface engineering of transport layer

Abstract This research presents interfacial engineering of large–area perovskite modules. The quality of the interface between the electron transport layer(ETL) and the perovskite layer are studied, because it significantly affects the optoelectronic performance of large–area module devices. In large–area fabrication, film uniformity and interfacial quality are critical, as the ETL/perovskite interface governs both electron extraction and transport efficiency, while also affecting the uniformity and crystallinity of the perovskite. To overcome these issues, using picosecond laser technique (P1,P2,P3) to fabricate large–area modules, integrating monolithic cells in series. Planar SnO2 and mesoporous TiO2 ETL are prepared. Results show that meso–type ETL structures are better suited for large–area modules. The modules with meso–type TiO2 exhibit fewer shunting issues and stronger emission in electroluminescence images. Photoluminescence mapping indicates improved structural uniformity of perovskite. The perovskite module with meso–type TiO2 achieve power conversion efficiency of 18.2% (4cm2) and maintain 80% of initial efficiency after 700 hours.

Development of GaN-Based, 6.6 kW, 450 V, Bi-Directional On-Board Charger with Integrated 1 kW, 12 V Auxiliary DC-DC Converter with High Power Density

Automotive-grade GaN power switches have recently been made available in the market from a growing number of semiconductor suppliers. The exploitation of this technology enables the development of very efficient power converters operating at much higher switching frequencies with respect to components implemented with silicon power devices. Thus, a new generation of automotive power components with an increased power density is expected to replace silicon-based products in the development of higher-performance electric and hybrid vehicles. 650 V GaN-on-silicon power switches are particularly suitable for the development of 3–7 kW on-board battery chargers (OBCs) for electric cars and motorcycles with a 400 V nominal voltage battery pack. This paper describes the design and implementation of a 6.6 kW OBC for electric vehicles using automotive-grade, 650 V, 25 mΩ, discrete GaN switches. The OBC allows bi-directional power flow, since it is composed of a bridgeless, interleaved, totem-pole PFC AC/DC active front end, followed by a dual active bridge (DAB) DC-DC converter. The OBC can operate from a single-phase 90–264 Vrms AC grid to a 200–450 V high-voltage (HV) battery and also integrates an auxiliary 1 kW DC-DC converter to connect the HV battery to the 12 V battery of the vehicle. The auxiliary DC-DC converter is a center-tapped phase-shifted full-bridge (PSFB) converter with synchronous rectification. At the low-voltage side of the auxiliary converter, 100 V GaN power switches are used. The entire OBC is liquid-cooled. The first prototype of the OBC exhibited a 96% efficiency and 2.2 kW/L power density (including the cooling system) at a 60 °C ambient temperature.

Computational Modeling of Graphene-Enhanced Back Surface Fields for Higher Efficiency in Copper Indium Gallium Selenide Solar Cell

The efficiency of CIGS (Copper Indium Gallium Selenide) solar cells has been significantly improved by incorporating Graphene Oxide (GO) or Graphene into their structure, specifically designed as Al/Tungsten Sulphoselenide (WSSe)/CIGS/GO or Graphene. GO or Graphene is employed as a back surface field to enhance charge carrier collection, with GO yielding better results than Graphene. This integration has resulted in a substantial increase in power conversion efficiency (PCE). The optimization process involved fine-tuning various parameters, including thickness adjustments and acceptor concentration levels. Moreover, the analysis addressed key factors such as shunt and series resistance, as well as the impact of temperature. The proposed design achieved a remarkable peak efficiency of 33.28%. In addition, extensive studies on temperature effects were conducted, offering deeper insights into the cell's performance under different conditions. Overall, this innovative structure shows great promise for future fabrication, offering enhanced performance and significant potential for advancing solar cell technology.

Quasi-solid-state monolithic DSSCs with optimized spacer layers and composite electrolytes for better efficiency and stability

In this study, high-performance quasi-solid-state monolithic dye-sensitized solar cells (QS-M-DSSCs) were designed using an optimized spacer layer architecture to enhance electrolyte transport and improve cell performance. Spacer layers, made from a combination of zirconium oxide (ZrO2) and titanium dioxide (TiO2), were precisely tuned to reduce mass-transport limitations. A 5.2 μm thick ZrO2/TiO2 layer provided good light reflectance and incident photon-to-current conversion efficiency compared to double layers of either material alone. Electrochemical impedance spectroscopy analysis of the m-DSSCs revealed that this architecture (photoelectrode TiO2 layer/ZrO2/TiO2 spacer layer/counter electrode catalyst layer) significantly increased recombination resistance, leading to an improvement in open-circuit voltage. As a result, acetonitrile iodide liquid-DSSCs using N719 dye achieved a high power conversion efficiency (PCE) of 8.45 %, surpassing cells with alternative spacer designs. For fully printable QS-M-DSSCs, printable gel electrolytes (PGEs) composed of polyethylene oxide and polymethyl methacrylate in 3-methoxypropionitrile (MPN) were employed. A 5 wt% PEO/PMMA composition demonstrated fast and efficient penetration of the PGEs through spacer layers. Moreover, incorporation of 4 wt% TiO2 nanoparticles into PGEs further enhanced their electrochemical properties, achieving a PCE (7.31 %) higher than cells with liquid electrolytes (6.72 %). QS-M-DSSCs demonstrated greater stability than liquid-state DSSCs.

Dimeric Acceptors Using Different Central Linkers to Manipulate Electronic and Morphological Properties

AbstractDimerized acceptors show promise in combining the high performance of small‐molecule non‐fullerene acceptors (NFAs) with the excellent stability of polymer acceptors. The central linking units that connect two acceptor molecules together have a profound impact on dimeric acceptor properties and structure‐performance relationships in blended thin films. It is seen that different linkers significantly affect the electronic properties and morphology in blended thin film. The electron‐donating linker elevates the absorption coefficient, affords a lower bandgap, and reduces energy loss, and thus better photovoltaic device performance. Better fibrillar morphology can be obtained. The best material DY‐EDOT‐based device shows a power conversion efficiency (PCE) of 18.21%, an open‐circuit voltage (Voc) of 0.924 V, a short‐circuit current density (Jsc) of 25.20 mA cm−2, a fill factor (FF) of 78.19%, which is among the highest value for dimerized acceptors. This study reveals the fundamental importance of linker units in determining the dimerized acceptor properties and provides useful strategies for developing oligomeric and polymeric acceptors, which is critical in simultaneously improving the performance and stability of organic solar cells (OSCs).

A theoretical study on the insights of designing and optimization of a CsSn(IxBr1-x)3 based solar cell

This work focuses on designing and optimizing a lead-free perovskite solar cell. The significance of band gap grading in obtaining better performance of the solar cell was studied in detail with CsSn(IxBr1-x)3 () being used as the active absorber material. The device showed a maximum power conversion efficiency (PCE) of when the interfacial defects were not considered. The optimum thickness was obtained to be 1 μm, and the corresponding doping concentration was 1020 cm-3. Further, a detailed discussion on the band diagrams, electric fields, and different recombination processes has been carried out in this work to get an idea about the varying PCE values at different operating conditions. The presence of Shockley-Read-Hall (SRH) recombination at various temperature values was observed, which partially contributed to the reduction in PCE values at higher temperatures. This work also discusses briefly about the probable losses involved with the device, which may be considered as the plausible reasons for obtaining PCE values less than the SQ limit. This information opens up a wide window for researchers to experimentally fabricate solar cells with proper cautions so that a device with PCE value exceeding Shockley Quisser (SQ) limit can be made available commercially.

Impact of Self-Assembled Monolayer Structural Design on Perovskite Phase Regulation, Hole-Selective Contact, and Energy Loss in Inverted Perovskite Solar Cells

Recent studies have shown that self-assembled molecule (SAM)-based hole-selective contacts (HSCs) offer a promising solution to the challenges faced by perovskite solar cells (PVSCs), including minimal material consumption, scalable production, high interface stability, and the use of environmentally friendly solvents. In this study, the efficacy of two designs of SAMs (Cz and PA) as HSCs in inverted PVSCs was investigated by comparing them with the conventional MeO-2PACz (MeO) SAM. Surface analyses showed that the surface of PA is smoother than that of Cz, which helps to reduce interfacial defects. Subsequent perovskite deposition exhibited a reduced formation of the PbI2 phase, incidiating that its phase modulation ability is superior to that of MeO. Further analyses demonstrate the superior charge extraction ability of PA as a result of reduced interfacial defects and non-radiative recombination at the HSC/perovskite interface. By further coupling with phenethylammonium iodide (PEAI) surface passivation, both interfaces of the perovskite film were optimized and the inverted ((FAPbI3)0.85(MAPbBr3)0.15)0.95(CsPbI3)0.05 (bandgap = 1.62eV) PVSC achieves a high power conversion efficiency (PCE) of 23.3% and a very high open-circuit voltage of 1.227V due to the largely reduced energy loss. In addition, the PA PVSC exhibits enhanced long-term thermal stability at 85°C in a nitrogen atmosphere.