shuhui

In article number https://doi.org/10.1002/adma.2019019661901966, Guichuan Xing, Yanlin Song, and co‐workers present a new low‐dimensional perovskite based on 1,4‐butanediamine (BEA), with the alternating ordered of diammonium and monoammonium cations in the interlayer space. Taking advantage of the short layer spacing and hydrogen bonding, a barrier‐free and balanced carrier‐transport pathway with an enhanced carrier‐diffusion mechanism is proposed. Due to the hydrophobicity of BEA, the new low‐dimensional perovskite exhibits excellent stability.

A fullerene derivative, [6,6]‐phenyl‐C₆₁‐butyric acid‐N,N‐dimethyl‐3‐(2‐thienyl)propanam ester (PCBB‐S‐N), is designed and synthesized to correct defects in electron‐transporting layers (ETLs) and perovskite films. Its use leads to a promising power conversion efficiency (PCE) of 21.08% for perovskite solar cells. Importantly, devices containing PCBB‐S‐N simultaneously realize excellent thermal stability and water resistance.

Abstract

The poor long‐term stability of organic–inorganic hybrid halide perovskite solar cells (pero‐SCs) remains a big challenge for their commercialization. Although strategies such as encapsulation, doping, and passivation have been reported, there remains a lack of understanding of the water resistance and thermal stability of pero‐SCs. A fullerene derivative, [6,6]‐phenyl‐C₆₁‐butyric acid‐N,N‐dimethyl‐3‐(2‐thienyl)propanam ester (PCBB‐S‐N) containing a functional sulfur atom and C_60, is synthesized and employed as electron transporting layer (ETL)/intermediary layer to targetedly heal the multitype defects in pero‐SCs or assist the growth of ETL, such as [6,6]‐phenyl‐C₆₁‐butyric acid methyl ester (PCBM), in planar p‐i‐n pero‐SCs. The repaired pero‐SCs can not only dramatically improve their power conversion efficiencies, but also address stability issues under moisture and high temperature. The corresponding mechanism of PCBB‐S‐N with targeted therapy effect in a device is systematically investigated by both experiments and theoretical calculation. This work demonstrates that the proposed fullerene derivative with finely tuned chemical structure can be a promising ETL candidate or intermediary to approach stable and efficient planar p‐i‐n pero‐SCs.

A new method is developed to synthesize SnO _x ‐Cl colloids and to realize an in situ and spontaneous ion‐exchange reaction during the perovskite film crystallization process. It is found that such ion exchange can perfectly passivate the interface defects and reduce energy loss at the interface.

Abstract

Interface engineering is of great concern in photovoltaic devices. For the solution‐processed perovskite solar cells, the modification of the bottom surface of the perovskite layer is a challenge due to solvent incompatibility. Herein, a Cl‐containing tin‐based electron transport layer; SnO _x ‐Cl, is designed to realize an in situ, spontaneous ion‐exchange reaction at the interface of SnO _x ‐Cl/MAPbI₃. The interfacial ion rearrangement not only effectively passivates the physical contact defects, but, at the same time, the diffusion of Cl ions in the perovskite film also causes longitudinal grain growth and further reduces the grain boundary density. As a result, an efficiency of 20.32% is achieved with an extremely high open‐circuit voltage of 1.19 V. This versatile design of the underlying carrier transport layer provides a new way to improve the performance of perovskite solar cells and other optoelectronic devices.

Balancing act: The indeno[1,2‐b]carbazole donor not only combines the characteristics of carbazole and fluorene, but also exhibits excellent thermal stability and high hole mobility as a result of the bulky planar structure. Hole‐transporting materials based on this methoxy‐free donor demonstrate a high efficiency and stability simultaneously, providing a promising strategy for developing efficient and stable perovskite‐based solar cells.

Abstract

With perovskite‐based solar cells (PSCs) now reaching efficiencies of greater than 20 %, the stability of PSC devices has become a critical challenge for commercialization. However, most efficient hole‐transporting materials (HTMs) thus far still rely on the state‐of‐the‐art methoxy triphenylamine (MOTPA) donor unit in which methoxy groups usually reduce the device stability. Herein, a carbazole‐fluorene hybrid has been employed as a methoxy‐free donor to construct organic HTMs. The indeno[1,2‐b]carbazole group not only inherits the characteristics of carbazole and fluorene, but also exhibits additional advantages arising from the bulky planar structure. Consequently, M129, endowed with indeno[1,2‐b]carbazole simultaneously exhibits a promising efficiency of over 20 % and superior long‐term stability. The hybrid strategy toward the methoxy‐free donor opens a new avenue for developing efficient and stable HTMs.

The fused‐ring acceptor IT‐M is added into an unfused‐core acceptor‐based binary blend of PBDB‐TF:HC‐PCIC. Notable fill factor enhancement and a broad compositional tolerance are achieved for the ternary solar cells. Thus, the power conversion efficiency is significantly improved from 11.14% for binary devices to 12.34% for ternary cells.

The ternary blend strategy has shown great potential to improve the photovoltaic performance of organic solar cells (OSCs). Usually, adopting two acceptors with similar chemical structures shows good compatibility but limited enhancement in performance, whereas adopting two acceptors with different chemical structures always has a compositional sensitivity issue. Herein, a highly efficient ternary OSC with an enhanced fill factor (FF) and a broad compositional tolerance is demonstrated by introducing the fused‐ring acceptor IT‐M to a binary blend based on an unfused‐core acceptor HC‐PCIC and polymer donor PBDB‐TF. Detailed studies on the optical, electrical, and morphological properties of ternary blends reveal the process of charge dynamics and work mechanisms in the ternary device. It is found that the addition of IT‐M into the PBDB‐TF:HC‐PCIC binary blend not only adapts to the parallel‐like model, but also optimizes the morphology and domain sizes in the ternary blend, resulting in a reduced trap‐assisted recombination and suppressed bimolecular recombination. Consequently, open‐circuit voltage (V _oc), short‐circuit current density (J _sc), and FF are synergistically enhanced, leading to an improved power conversion efficiency (PCE) of 12.34% with a high V _oc of 0.88 V, an increased J _sc of 18.69 mA cm⁻², and an enhanced FF of 73.82% for the ternary device with 5% IT‐M content. Moreover, the PCEs of ternary OSCs remain above 11% within an IT‐M ratio of 2.5–50%, exhibiting a broad compositional tolerance, which is rarely reported in fullerene‐free ternary OSCs.

The interface and bulk defects of perovskite solar cells are distinguished and quantified, and are for the first time traced in situ using an expanded admittance model. A fullerene derivative [6, 6]‐phenyl‐C61‐butyric acid (PCBA) is introduced into the TiO₂/perovskite interface to release the interface stress.

Abstract

The stability issue that is obstructing commercialization of the perovskite solar cell is widely recognized, and tremendous effort has been dedicated to solving this issue. However, beyond the apparent thermal and moisture stability, more intrinsic semiconductor mechanisms regarding defect behavior have yet to be explored and understood. Herein, defects are quantified; especially interface defects, within the cell to reveal their impact on device performance and especially stability. Both the bulk and interface defects are distinguished and traced in situ using an expanded admittance model when the cell degrades in its efficiency under illumination or voltage. The electric field‐induced interface, rather than bulk defects, is found to have a direct correlation to stability. Releasing the interface strain using a fullerene derivative is an effective way to suppress interface defect formation and improve stability. Overall, this work provides a quantitative approach to probing the semiconductor mechanism behind the stability issue, and the inherent correlation discovered here among the electric field, interface strain, interface defects, and cell stability has important implications for ongoing device stability engineering.

A power conversion efficiency of 13.36% in ternary organic photovoltaics is obtained by carefully picking materials with good compatibility and complementary absorption spectra, as well as well‐matched energy levels with efficient energy transfer.

Abstract

Organic photovoltaics (OPVs) are fabricated with PM6 as donor and T6Me, IT‐2F, or their mixture as acceptor. A 13.36% power conversion efficiency (PCE) is achieved from the optimized ternary OPVs with 50 wt% IT‐2F in acceptors, which is attributed to the enhanced photon harvesting of ternary active layers and improved exciton utilization efficiency through energy transfer from IT‐2F to T6Me. The efficient energy transfer from IT‐2F to T6Me can be confirmed from the photoluminescence spectra of neat and blend films, which may provide additional channels to enhance exciton utilization efficiency for achieving short‐circuit current density (J _SC) improvement of ternary OPVs. It should be highlighted that the fill factor (FF) of ternary OPVs can be monotonously increased along with the incorporation of IT‐2F, indicating the gradually optimized phase separation degree of ternary active layers. The third component IT‐2F plays a key role in optimizing phase separation as a morphology regulator. Over 8% PCE improvement is achieved in the optimized ternary OPVs compared with the over 12% PCEs of the corresponding binary OPVs, respectively. This work indicates that the performance of ternary OPVs can be well optimized by carefully picking materials with good compatibility and complementary absorption spectra, as well as the appropriate energy levels.

Herein, a facile strategy that can carry out double passivation to improve the performance of perovskite solar cells (PSCs) is demonstrated. By using the dilute halide salt PEABr solution to treat the perovskite film, PbI₂ can precipitate from the perovskite. Both PEABr and PbI₂ can passivate the perovskite film; double passivation improves the performance of PSCs significantly.

Material passivation is essential to enhance the quality of perovskite materials and boost the performance of perovskite solar cells (PSCs). However, most of the previous reports only paid attention to improving the quality of perovskite films by adopting single passivation. Here, a facile strategy that can carry out double passivation to improve the performance of PSCs is demonstrated. By using the dilute halide salt PEABr solution to treat the perovskite film, PbI₂ can precipitate from the perovskite. Both PEABr and PbI₂ can passivate the perovskite film, and by combining PEABr and PbI₂, the double passivation improves the performance of PSCs significantly. Very high short‐circuit current density of 24.30 mA cm⁻², open‐circuit voltage of 1.10 V, and fill factor of 79.75% are achieved which lead to a surprising efficiency of 21.32% for the passivated device. The improved efficiency is mainly according to the available surface passivation of the perovskite material, leading to repressed nonradiative recombination and unhindered charge collection. In addition, the passivated device exhibits better power conversion efficiency stability relative to the control device.

Small‐molecule electrolyte (C6‐E‐OTs) hybridized ZnO layer is provided as the electron transporting layer. The device based on the blend of PTB7 and PC₇₁BM as the active layer shows an enhanced power conversion efficiency (PCE) from 7.6% based on ZnO to 8.8% using the C6‐E‐OTs hybridized ZnO layer. Hybridized ZnO layer process can overcome the limitation faced by the thickness tolerance of interlayer.

Abstract

Small‐molecule electrolyte (C6‐E‐OTs) hybridized ZnO layer is provided as the electron transporting layer. The device based on the blend of PTB7 and PC₇₁BM as the active layer shows an enhanced power conversion efficiency (PCE) from 7.6% based on ZnO to 8.8% using the C6‐E‐OTs hybridized ZnO layer. The device can be further improved by simultaneously using a C6‐E‐OTs hybridized ZnO layer and a 5 nm thick C6‐E‐OTs as the interlayer. The synergy effect of hybridization and interlayer enhanced the PCE of the device to 8.9%, which is a 17.1% increase in comparison with the device based on ZnO. The presence of C6‐E‐OTs hybridized ZnO and a 5 nm of C6‐E‐OTs as the interlayer in the device with PTB7‐Th as the donor significantly improves the PCE from 8.0% based on ZnO to 9.4%, resulting in a 17.5% enhancement. Main contribution for enhancing the PCE of the device is the improved J _sc, which results from the reduction of energy offset at the cathode interface. Thus, hybridized ZnO layer process can overcome the limitation faced by the thickness tolerance of interlayer.

Thionation is a straightforward strategy to dramatically boost the performance of dopant‐free polymeric hole‐transporting materials (HTMs) for perovskite solar cells. Upon HTM thionation, a nearly 40% enhancement in the power conversion efficiency of the corresponding devices is observed. Such an increase is attributed to the enhancement of both the hole transport within the HTM and the interfacial hole transfer dynamics.

Abstract

To date, the most efficient perovskite solar cells (PSCs) require hole‐transporting materials (HTMs) that are doped with hygroscopic additives to improve their performance. Unfortunately, such dopants negatively impact the overall PSCs stability and add cost and complexity to the device fabrication. Hence, there is a need to investigate new strategies to boost the typically modest performance of dopant‐free HTMs for efficient and stable PSCs. Thionation is a simple and single‐step approach to enhance the carrier‐transport capability of organic semiconductors, yet still completely unexplored in the context of HTMs for PSCs. In this work, a novel polymeric semiconductor, P1, based on a diketopyrrolopyrrole (DPP) moiety, is proposed as a dopant‐free HTM. Its modest performance in PSCs (power conversion efficiency (PCE) = 7.1%) is significantly enhanced upon thionation of the DPP moiety. The resulting dithioketopyrrolopyrrole‐based HTM, P2, leads to PSCs with nearly 40% performance improvement (PCE = 9.7%) compared to devices based on the nonthionated HTM (P1). Furthermore, thionation also remarkably boosts the shelf‐storage and thermal stability with respect to traditional 2,2′,7,7′‐tetrakis(N,N‐di‐p‐methoxyphenylamine)‐9,9′‐spirobifluorene‐based PSCs. This work provides useful insights to further design effective dopant‐free HTMs employing the straightforward one‐step thionation strategy for efficient and stable PSCs.

Publication date: November 2019

Source: Nano Energy, Volume 65

Author(s): Van-Dang Tran, S.V.N. Pammi, Byeong-Ju Park, Yire Han, Cheolho Jeon, Soon-Gil Yoon

Graphical abstract

Hybrid halide perovskites and ferroelectric perovskites are two different classes of materials with analogies in their structure. Such analogies and state‐of‐the‐art technologies based on these materials are reviewed so that future multisource energy conversion devices (which are capable of utilizing piezoelectric, pyroelectric, photovoltaic, and thermoelectric effects simultaneously) and storage devices can be created in a holistic manner.

Abstract

An insight into the analogies, state‐of‐the‐art technologies, concepts, and prospects under the umbrella of perovskite materials (both inorganic–organic hybrid halide perovskites and ferroelectric perovskites) for future multifunctional energy conversion and storage devices is provided. Often, these are considered entirely different branches of research; however, considering them simultaneously and holistically can provide several new opportunities. Recent advancements have highlighted the potential of hybrid perovskites for high‐efficiency solar cells. The intrinsic polar properties of these materials, including the potential for ferroelectricity, provide additional possibilities for simultaneously exploiting several energy conversion mechanisms such as the piezoelectric, pyroelectric, and thermoelectric effect and electrical energy storage. The presence of these phenomena can support the performance of perovskite solar cells. The energy conversion using these effects (piezo‐, pyro‐, and thermoelectric effect) can also be enhanced by a change in the light intensity. Thus, there lies a range of possibilities for tuning the structural, electronic, optical, and magnetic properties of perovskites to simultaneously harvest energy using more than one mechanism to realize an improved efficiency. This requires a basic understanding of concepts, mechanisms, corresponding material properties, and the underlying physics involved with these effects.

The studies from the steady‐state and time‐dependent measurements indicate that the extended absorption range, short charge carrier extraction time, and high charge carrier mobility by the non‐fullerene electron acceptors in the photoactive layer are responsible for enhanced photocurrent in ternary organic solar cells.

Ternary organic solar cells, a single active layer comprising three different components, are demonstrated to be one of the most efficient ways to approach high‐performance organic solar cells. But nevertheless, most of the ternary organic solar cells are characterized by steady‐state measurements, which are helpful but inadequate to fully understand the underlying charge carrier behavior at a short time scale. Herein, a comparison of the steady‐state and time‐dependent measurements is used to investigate the functionality of non‐fullerene electron acceptors in ternary organic solar cells. The steady‐state measurements indicate that non‐fullerene electron acceptors enlarge the absorption range of the photoactive layer, suppress charge carrier recombination, reduce charge carrier transfer resistance, and thereby increase photocurrent in ternary organic solar cells. The time‐dependent measurements demonstrate that a short charge carrier extraction time and a high charge carrier mobility are responsible for enhanced photocurrent in ternary organic solar cells. A comprehensive method understanding the underlying of enhanced efficiency of ternary organic solar cells is provided herein.

This study presents a reasonable strategy for designing 2DBDT‐chlorinated thiophene‐based donor polymers with balanced molecular weight and solubility by modifying the structure of previously reported low cost P(Cl) to achieve high‐efficiency polymer solar cells (PSCs). As a result, the new P(Cl–Cl)(BDD = 0.2) reaches a high power conversion efficiency of 13.9% using eco‐friendly solvents for commercialization of PSCs.

Abstract

To industrialize nonfullerene polymer solar cells (NFPSCs), the molecular design of the donor polymers must feature low‐cost materials and a high overall yield. Two chlorinated thiophene‐based polymers, P(F–Cl) and P(Cl–Cl), are synthesized by introducing halogen effects like fluorine (F) and chlorine (Cl) to the previously reported P(Cl), which exhibits low complexity. However, the molecular weights of these polymers are insufficient owing to their low solubility, which in turn is caused by introducing rigid halogen atoms during the polymerization. Thus, they show relatively low power conversion efficiencies (PCEs) of 11.8% and 10.3%, respectively. To overcome these shortcomings, two new terpolymers are designed and synthesized by introducing a small amount of 1,3‐bis(5‐bromothiophen‐2‐yl)‐5,7‐bis(2‐ethylhexyl)benzo[1,2‐c:4,5‐c′]dithiophene‐4,8‐dione (BDD) unit into each backbone, namely, P(F–Cl)(BDD = 0.2) and P(Cl–Cl)(BDD = 0.2). As a result, both polymers remain inexpensive and show a better molecular weight–solubility balance, achieving high PCEs of 12.7% and 13.9%, respectively, in NFPSCs processed using eco‐friendly solvents.

Progress in the development of expitaxial two‐terminal GaInP/GaAs/Si triple‐junction solar cells is reported. By reducing the defect density in the metamorphic III–V layers to a value of 2.2 × 10⁷ cm⁻², the conversion efficiency is increased from 19.7% to 22.3% under AM1.5g conditions. A detailed characterization of the device is provided to identify the main loss mechanisms.

III–V on Si multijunction solar cells exceede the efficiency limit of Si single‐junction devices but are often challenged by expensive layer transfer techniques. Here, progress in the development of direct epitaxial growth for GaInP/GaAs/Si triple‐junction solar cells is reported. III–V absorbers with a total thickness of 4.9 μm are grown onto a Si bottom cell using metal organic vapor phase epitaxy. A new record efficiency of 22.3% under AM1.5g conditions is reached herein, outperforming the previous value of 19.7%. This improvement is possible through better nucleation conditions for the first GaP layer on Si and consequently the reduction of threading dislocations within the III–V absorbers from 1.4 × 10⁸ to 2.2 × 10⁷ cm⁻². Further efficiency improvements toward 30% require even lower threading dislocation densities in the order of 1 × 10⁶ cm⁻², better light trapping in the Si bottom cell, and a reduction of parasitic absorption within the GaAs _y P_1–y graded buffer.

Publication date: 18 September 2019

Source: Joule, Volume 3, Issue 9

Author(s): Henk J. Bolink