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The effect of the zinc concentration on the performance of solution‐processed indium gallium zinc oxide (IGZO), as an electron transport layer for an inverted polymer solar cell based on PTB7:PC71BM, is investigated. The performances of the devices have been optimized by tuning the concentrations. The IGZO films significantly enhance the power conversion efficiency of the device from 6.22% to 8.72%.

Organic polymer semiconductor‐based polymer solar cells (PSCs) are drawing tremendous research interest for their superior electrical, structural, optical, mechanical, and chemical properties. During the last two decades, immense efforts have been made toward the development of PSCs. Generally, poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is used as hole transport layer (HTL) of PSCs to improve hole extraction efficiency, but highly acidic PEDOT:PSS reduces device lifetime by destroying indium tin oxide (ITO) electrodes and active layers. To avoid this, some have attempted to develop inverted structured PSCs with different electron transport layers (ETLs); however, the power conversion efficiency (PCE) of these devices is limited owing to low electron mobility of their ETLs. Therefore, an attempt is made to improve the PCE of an inverted‐structured PSC by using indium gallium zinc oxide (IGZO) with optimized amount of indium (In), gallium (Ga), and zinc (Zn). Inverted PSCs with ZnO or IGZO (having various molar ratios of In, Ga, and Zn) as ETL with the structure ITO/ETL/PTB7:PC₇₁BM/MoO₃/Al are constructed. The PCE of the inverted PSC can be increased from 6.22% to 8.72% by using IGZO with an optimized weight ratio of In, Ga, and Zn as an ETL.

Nature Materials, Published online: 04 January 2021; doi:10.1038/s41563-020-00865-5

The mystery of the buried interface in perovskite photovoltaics is deciphered by combining advanced spectroscopy techniques with a lift‐off strategy. The findings open a new avenue to understanding performance losses and thus the design of unique passivation strategies to remove imperfections at the top surfaces and buried interfaces of perovskite photovoltaics, resulting in substantial enhancement in device performance.

Abstract

Understanding the fundamental properties of buried interfaces in perovskite photovoltaics is of paramount importance to the enhancement of device efficiency and stability. Nevertheless, accessing buried interfaces poses a sizeable challenge because of their non‐exposed feature. Herein, the mystery of the buried interface in full device stacks is deciphered by combining advanced in situ spectroscopy techniques with a facile lift‐off strategy. By establishing the microstructure–property relations, the basic losses at the contact interfaces are systematically presented, and it is found that the buried interface losses induced by both the sub‐microscale extended imperfections and lead‐halide inhomogeneities are major roadblocks toward improvement of device performance. The losses can be considerably mitigated by the use of a passivation‐molecule‐assisted microstructural reconstruction, which unlocks the full potential for improving device performance. The findings open a new avenue to understanding performance losses and thus the design of new passivation strategies to remove imperfections at the top surfaces and buried interfaces of perovskite photovoltaics, resulting in substantial enhancement in device performance.

Publication date: April 2021

Source: Nano Energy, Volume 82

Author(s): Jingnan Wu, Qunping Fan, Minghai Xiong, Qiutang Wang, Kai Chen, Haiqin Liu, Mengyuan Gao, Long Ye, Xia Guo, Jin Fang, Qing Guo, Wenyan Su, Zaifei Ma, Zheng Tang, Ergang Wang, Harald Ade, Maojie Zhang

Nonfullerene acceptors dominate organic solar cell research due to their promising high device efficiencies. However, key challenges for achieving high stability in commercially viable devices still remain. In this review, recent progress and challenges toward stable organic solar cells are discussed correlating molecular design and device engineering to device stability.

Abstract

Organic solar cells (OSCs) based on nonfullerene acceptors (NFAs) have made significant breakthrough in their device performance, now achieving a power conversion efficiency of ≈18% for single junction devices, driven by the rapid development in their molecular design and device engineering in recent years. However, achieving long‐term stability remains a major challenge to overcome for their commercialization, due in large part to the current lack of understanding of their degradation mechanisms as well as the design rules for enhancing their stability. In this review, the recent progress in understanding the degradation mechanisms and enhancing the stability of high performance NFA‐based OSCs is a specific focus. First, an overview of the recent advances in the molecular design and device engineering of several classes of high performance NFA‐based OSCs for various targeted applications is provided, before presenting a critical review of the different degradation mechanisms identified through photochemical‐, photo‐, and morphological degradation pathways. Potential strategies to address these degradation mechanisms for further stability enhancement, from molecular design, interfacial engineering, and morphology control perspectives, are also discussed. Finally, an outlook is given highlighting the remaining key challenges toward achieving the long‐term stability of NFA‐OSCs.

Highly efficient CsPbI_1.5Br_1.5 perovskite solar cells (PSCs) are achieved via introducing fluorescein isothiocyanate (FITC) organic dye as passivator. FITC not only reduces the metal ion related trap states but also improves film crystallinity, resulting in an enhancement of device efficiency from 12.3% to 14.05%. In addition, it is demonstrated that CsPbI_1.5Br_1.5 perovskite shows the optimal halide composition for inorganic PSCs.

Abstract

All‐inorganic perovskite solar cells (PSCs) have recently received growing attention as a promising template to solve the thermal instability of organic–inorganic PSCs. However, the thermodynamic phase instability and relatively low device efficiency pose challenges. Herein, highly efficient and stable CsPbI_1.5Br_1.5 compositional perovskite‐based inorganic PSCs are fabricated using an organic dye, fluorescein isothiocyanate (FITC), as a passivator. The carboxyl and thiocyanate groups of FITC not only minimize the trap states by forming interactions with the under‐coordinated Pb²⁺ ions but also significantly increase the grain size and improve the crystallinity of the perovskite films during annealing. Consequently, perovskite films with superior optoelectronic properties, prolonged carrier lifetime, reduced trap density, and improved stability are obtained. The resulting device yields a champion efficiency of 14.05% with negligible hysteresis, which presents the highest reported efficiency for inorganic CsPbI_1.5Br_1.5 solar cells reported thus far. In addition, FITC can be generally adopted as attractive passivator to improve the performance of CsPbI₂Br‐ and CsPbIBr₂‐based PSCs. Furthermore, with a comprehensive comparison of mixed‐halide inorganic perovskites, it is demonstrated that CsPbI_1.5Br_1.5 compositional perovskite is a promising candidate with the optimal halide composition for high‐performance inorganic PSCs.

Field‐induced formation of dopant‐free radial junctions at the Al₂O₃/n‐c‐Si (crystalline silicon) interface is demonstrated. Atomic layer deposition of Al₂O₃ conformally coats tapered c‐Si microwire arrays to form the radial junctions. A dopant‐free radial junction solar cell is fabricated based on this technique. At 20.1%, the device obtains the highest efficiency compared with that of previously reported radial junction solar cells.

Abstract

Radial junctions on crystalline silicon (c‐Si) microwire structures considerably reduce the diffusion length of photoinduced minority carriers required for energy generation by decoupling light absorption and carrier separation in orthogonal spatial directions. Hence, radial junctions mitigate the need for high‐purity materials, and thus reduce the fabrication cost of c‐Si solar cells. In this study, the formation of dopant‐free radial junctions from atomic layer deposition (ALD) of Al₂O₃ on an n‐c‐Si microwire surface is reported. ALD‐Al₂O₃ generates a p⁺ inversion layer, which eventually forms the radial junction on the n‐c‐Si surface. The width of depletion region induced by the p⁺ inversion layer is calculated from PC1D simulation as 900 nm. The fabricated dopant‐free radial junction c‐Si solar cells exhibit a power conversion efficiency of 20.1%, which is higher than those of previously reported microwire‐based radial junction solar cells. Notably, internal quantum efficiencies of over 90% are obtained in the 300–980 nm wavelength region, thereby verifying the successful formation of radial junctions.

Flexible organic solar cells (OSCs) come to the forefront of organic electronics. It's critical to develop high‐merit flexible transparent electrodes (FTEs). The work covers the frontier progress of PEDOT:PSS, graphene, metallic nanostructures, metal oxide/metal/metal oxide, Mxene and hybrid electrodes. It raises the awareness for the importance of developing the FTEs and reveals the critical role in flexible OSCs.

Abstract

Substantial effort has been devoted to both chemical doping and design of flexible transparent electrodes (FTEs) for flexible organic solar cells (OSCs) in the past decade. Poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate), graphene, metal nanostructures, metal oxide/ultrathin metal/metal oxide, Mxene, and their hybrid electrodes emerge to be the most promising flexible conducting materials over indium tin oxide. The FTE fabrications play a critical role in flexible OSCs. This feature review article summarizes the current status on the researches of the FTEs including various approaches and strategies to boost the conductivity, work function, mechanical flexibility, wettability, etc, which directly affect the performances of the flexible OSCs. The most cutting edge progresses on both FTEs and flexible OSCs are highlighted along the line. Advantages and plausible issues are pointed out. Perspectives are provided that can advance the developments of the flexible OSCs. This review raises the awareness for the importance of developing plenty of FTEs and reveals their critical role in flexible OSCs.

This Minireview describes developments in all‐polymer solar cells containing a new type of n‐type conjugated polymer, polymerized small‐molecule acceptors (PSMAs). PSMAs combine the merits of small‐molecule acceptors (narrow band gap, strong absorption, and suitable electronic energy levels) with the good film formation, higher morphology and light‐irradiation stability of polymers.

Abstract

All‐polymer solar cells (all‐PSCs) have drawn tremendous research interest in recent years, due to their inherent advantages of good film formation, stable morphology, and mechanical flexibility. The most representative and most widely used n‐CP acceptor was the naphthalene diimide based D‐A copolymer N2200 before 2017, and the power conversion efficiency (PCE) of the all‐PSCs based on N2200 reached over 8% in 2016. However, the low absorption coefficient of N2200 in the near‐infrared (NIR) region limits the further increase of its PCE. In 2017, we proposed a strategy of polymerizing small‐molecule acceptors (SMAs) to construct new‐generation polymer acceptors. The polymerized SMAs (PSMAs) possess low band gap and strong absorption in the NIR region, which attracted great attention and drove the PCE of the all‐PSCs to over 15% recently. In this Minireview we explain the design strategies of the molecular structure of PSMAs and describe recent research progress. Finally, current challenges and future prospects of the PSMAs are analyzed and discussed.

The power conversion efficiencies (PCEs) of single‐junction organic solar cells have now reached over 18%. Recent progress that has been made in understanding the morphology and the device photophysics of high performing polymer:non‐fullerene acceptor blends and some of the major challenges that must be overcome to attain PCEs of over 20% are highlighted.

Abstract

The power conversion efficiencies (PCEs) of single‐junction organic solar cells (OSC) have now reached over 18%. This rapid recent progress can be attributed to the development of new nonfullerene electron acceptors (NFAs) that are paired with suitable high performing polymer electron donors. Substantial improvements in the PCEs and long‐term stability enabled by NFA OSCs have allowed the development and integration of these systems into many niche and novel applications. Here, the recent progress that has been made in understanding the device photophysics of high performing polymer:NFA blends is highlighted. As the bulk heterojunction morphology is intrinsically linked to the device photophysics, this review focuses on studies that have provided noteworthy morphological insights using advanced techniques such as solid‐state NMR and resonant soft X‐ray scattering. Through this, some of the major challenges that must be overcome to attain PCEs of over 20% in NFA OSCs are addressed.

Conformation effects of Y6‐type acceptors are systematically studied based on asymmetric design strategies. Z‐shape and W‐shape conformations‐based acceptors can help reduce energy loss in devices through significantly suppressed nonradiative energy loss. Benefiting from the high open‐circuit voltage of BP5T‐4F in the devices, ternary organic solar cells based on PM6:BP5T‐4F:CH1007 achieve a 17.2% efficiency.

Abstract

Y6, as a state‐of‐the‐art nonfullerene acceptor (NFA), is extensively optimized by modifying its side chains and terminal groups. However, the conformation effects on molecular properties and photovoltaic performance of Y6 and its derivatives have not yet been systematically studied. Herein, three Y6 analogs, namely, BP4T‐4F, BP5T‐4F, and ABP4T‐4F, are designed and synthesized. Owing to the asymmetric molecular design strategies, three representative molecular conformations for Y6‐type NFAs are obtained through regulating the lateral thiophene orientation of the fused core. It is found that conformation adjustment imposes comprehensive effects on the molecular properties in neat and blend films of these NFAs. As a result, organic solar cells (OSCs) fabricated with PM6:BP4T‐4F, PM6:BP5T‐4F, and PM6:ABP4T‐4F show high power conversion efficiency of 17.1%, 16.7%, and 15.2%, respectively. Interestingly, these NFAs with different conformations also show reduced energy loss (E _loss) in devices via gradually suppressed nonradiative E _loss. Moreover, by employing a selenium‐containing analog, CH1007, as the complementary third component, ternary OSCs based on PM6:BP5T‐4F:CH1007 (1:1.02:0.18) achieve a 17.2% efficiency. This work helps shed light on engineering the molecular conformation of NFAs to achieve high efficiency OSCs with reduced voltage loss.

A new class of polymer acceptors (P _As, P(BDT2BOY5‐X)) consisting of benzodithiophene (BDT) and non‐fullerene small molecule‐accepting units is developed, which shows excellent material compatibility with an efficient BDT‐based polymer donor (P _D). The resulting all‐polymer solar cells show excellent photovoltaic efficiency, thermal stability, and mechanical robustness at the same time, benefitting from the high chemical and molecular compatibilities between P _D and P _A.

Abstract

All‐polymer solar cells (all‐PSCs) are a highly attractive class of photovoltaics for wearable and portable electronics due to their excellent morphological and mechanical stabilities. Recently, new types of polymer acceptors (P _As) consisting of non‐fullerene small molecule acceptors (NFSMAs) with strong light absorption have been proposed to enhance the power conversion efficiency (PCE) of all‐PSCs. However, polymerization of NFSMAs often reduces entropy of mixing in PSC blends and prevents the formation of intermixed blend domains required for efficient charge generation and morphological stability. One approach to increase compatibility in these systems is to design P _As that contain the same building blocks as their polymer donor (P _D) counterparts. Here, a series of NFSMA‐based P _As [P(BDT2BOY5‐X), (X = H, F, Cl)] are reported, by copolymerizing NFSMA (Y5‐2BO) with benzodithiophene (BDT), a common donating unit in high‐performance P _Ds such as PBDB‐T. All‐PSC blends composed of PBDB‐T P _D and P(BDT2BOY5‐X) P _A show enhanced molecular compatibility, resulting in excellent morphological and electronic properties. Specifically, PBDB‐T:P(BDT2BOY5‐Cl) all‐PSC has a PCE of 11.12%, which is significantly higher than previous PBDB‐T:Y5‐2BO (7.02%) and PBDB‐T:P(NDI2OD‐T2) (6.00%) PSCs. Additionally, the increased compatibility of these all‐PSCs greatly improves their thermal stability and mechanical robustness. For example, the crack onset strain (COS) and toughness of the PBDB‐T:P(BDT2BOY5‐Cl) blend are 15.9% and 3.24 MJ m^–3, respectively, in comparison to the PBDB‐T:Y5‐2BO blends at 2.21% and 0.32 MJ m^–3.

Photoelectrochemical (PEC) water splitting is an attractive method to produce carbon dioxide emission‐free hydrogen fuel. However, most PEC devices are small and lacking the durability and reproducibility necessary for commercial applications. In article number 2002706, Nemanja Danilovic and co‐workers describe the scale‐up of an integrated PEC platform from 1 to 8 cm², with repeatable measurement results and good durability in two markedly different locations. (Image credit: Yalili Naranjo Chavez).

The moisture instability and unscalable fabrication protocols are still unsolved and blocking FACs‐based perovskite solar cells’ further applications. Here, high‐quality FACsPbI₃ films are fabricated by crown ether tailoring (which chelated with Cs⁺/Pb²⁺ ions) to inhibit the moisture invasion and stabilize the α‐phase FACsPbI₃, producing large‐area perovskite films and improving solar module performance.

Abstract

FACs‐based (FA⁺, formamidinium and Cs⁺, cesium) perovskite solar cells have gained great attention due to their remarkable light and thermal stabilities toward practical application of perovskite modules. However, the moisture instability and difficulty in scalable fabrication are still the main obstacles blocking their photovoltaic applications in current status. Here, the employment of novel interaction between crown ether with metal cations is introduced to tailor the uniform growth and inhibit moisture invasion during the crystallization of α‐phase FACsPbI₃, yielding the successful synthesis of high‐quality perovskite films in a large scale. Consequently, perovskite solar cells (PSC) modules in the total area of 4 × 4 and 10 × 10 cm² are readily fabricated with respective champion efficiencies of 16.69% and 13.84% and excellent stability over 1000 h. This facile scaling‐up strategy assisted by crown ether has shown great promise for pursuing efficient and highly stable large‐area PSC modules.

A defect‐resolved mobility measurement (DRMM) method is developed, enabling the evaluation of effective majority carrier mobility of highly anisotropic materials such as antimony chalcogenides directly from a working device. This method provides a reliable approach to the investigation of the carrier transport mechanisms of Sb₂Se₃ and Sb₂S₃ solar cells and other anisotropic low‐dimensional crystal semiconductor devices.

Majority carrier mobility is one of the most fundamental and yet important carrier transport parameters determining the optimal device architecture and performance of the emerging antimony chalcogenide solar cells. However, carrier mobility measurements based on the Hall effect have limitations for these highly anisotropy materials due to the discrepancy of transport directions under Hall measurement and device operation. Herein, a defect‐resolved mobility measurement (DRMM) method enabling the evaluation of effective majority carrier mobility from a working device without such limitations is presented. Using this method, comprehensive information about the carrier transport in representative Sb₂S₃ and Sb₂Se₃ solar cells is extracted. Though with preferred [hk1]‐crystalline orientation, Sb₂S₃ and Sb₂Se₃ still suffer from extremely low carrier mobility and low carrier density, respectively, resulting in large bulk resistance and poor carrier collection efficiency. Further crystalline structure analysis discloses that crystalline defects such as dislocations may significantly constrain carrier transport in these low‐dimensional materials. These results suggest that a p‐i‐n device architecture with fully depleted absorber is a promising optimization approach for further efficiency advances of antimony chalcogenide solar cells.