Showing papers on "Polymer solar cell published in 2017"
TL;DR: The effects of the fluorine atom number and position on electronic properties, charge transport, film morphology, and photovoltaic properties are investigated.
Abstract: We design and synthesize four fused-ring electron acceptors based on 6,6,12,12-tetrakis(4-hexylphenyl)-indacenobis(dithieno[3,2-b;2′,3′-d]thiophene) as the electron-rich unit and 1,1-dicyanomethylene-3-indanones with 0–2 fluorine substituents as the electron-deficient units. These four molecules exhibit broad (550–850 nm) and strong absorption with high extinction coefficients of (2.1–2.5) × 105 M–1 cm–1. Fluorine substitution downshifts the LUMO energy level, red-shifts the absorption spectrum, and enhances electron mobility. The polymer solar cells based on the fluorinated electron acceptors exhibit power conversion efficiencies as high as 11.5%, much higher than that of their nonfluorinated counterpart (7.7%). We investigate the effects of the fluorine atom number and position on electronic properties, charge transport, film morphology, and photovoltaic properties.
779 citations
TL;DR: Results show that fluorinated ITIC-Th1 exhibits redshifted absorption, smaller optical bandgap, and higher electron mobility than the nonfluorinated IT IC-Th, and nonfullerene organic solar cells (OSCs) based on fluorinatedITIC- Th1 electron acceptor and a wide-bandgap polymer donor FTAZ based on benzodithiophene and benzotriazole exhibit power conversion efficiency as high as 12.1%.
Abstract: A new fluorinated nonfullerene acceptor, ITIC-Th1, has been designed and synthesized by introducing fluorine (F) atoms onto the end-capping group 1,1-dicyanomethylene-3-indanone (IC). On the one hand, incorporation of F would improve intramolecular interaction, enhance the push-pull effect between the donor unit indacenodithieno[3,2-b]thiophene and the acceptor unit IC due to electron-withdrawing effect of F, and finally adjust energy levels and reduce bandgap, which is beneficial to light harvesting and enhancing short-circuit current density (JSC ). On the other hand, incorporation of F would improve intermolecular interactions through CF···S, CF···H, and CF···π noncovalent interactions and enhance electron mobility, which is beneficial to enhancing JSC and fill factor. Indeed, the results show that fluorinated ITIC-Th1 exhibits redshifted absorption, smaller optical bandgap, and higher electron mobility than the nonfluorinated ITIC-Th. Furthermore, nonfullerene organic solar cells (OSCs) based on fluorinated ITIC-Th1 electron acceptor and a wide-bandgap polymer donor FTAZ based on benzodithiophene and benzotriazole exhibit power conversion efficiency (PCE) as high as 12.1%, significantly higher than that of nonfluorinated ITIC-Th (8.88%). The PCE of 12.1% is the highest in fullerene and nonfullerene-based single-junction binary-blend OSCs. Moreover, the OSCs based on FTAZ:ITIC-Th1 show much better efficiency and better stability than the control devices based on FTAZ:PC71 BM (PCE = 5.22%).
644 citations
TL;DR: In this paper, the authors expose a link between electron-vibrations coupling and non-radiative recombinations, derive a new limit for the efficiency of organic solar cells, and redefine their optimal optical gap.
Abstract: The conversion efficiency of organic solar cells suffers from their low open-circuit voltages. Here, the authors expose a link between electron-vibrations coupling and non-radiative recombinations, derive a new limit for the efficiency of organic solar cells, and redefine their optimal optical gap.
462 citations
TL;DR: A kind of novel fused-ring small molecular acceptor, whose planar conformation can be locked by intramolecular noncovalent interaction, which will be promising in developing a new acceptor for high efficiency polymer solar cells.
Abstract: We have developed a kind of novel fused-ring small molecular acceptor, whose planar conformation can be locked by intramolecular noncovalent interaction. The formation of planar supramolecular fused-ring structure by conformation locking can effectively broaden its absorption spectrum, enhance the electron mobility, and reduce the nonradiative energy loss. Polymer solar cells (PSCs) based on this acceptor afforded a power conversion efficiency (PCE) of 9.6%. In contrast, PSCs based on similar acceptor, which cannot form a flat conformation, only gave a PCE of 2.3%. Such design strategy, which can make the synthesis of small molecular acceptor much easier, will be promising in developing a new acceptor for high efficiency polymer solar cells.
445 citations
TL;DR: In this paper, Essig et al. fabricate very efficient dual-and triple-junction solar cells by placing one or two III-V solar cells on top of a silicon solar cell.
Abstract: To improve the efficiency of photovoltaic devices while keeping the same spatial footprint, solar cells can be stacked on top of each other. Here, Essig et al. fabricate very efficient dual-junction and triple-junction solar cells by placing one or two III–V solar cells on top of a silicon solar cell.
429 citations
TL;DR: A strategy to synthesize a high-performance polymer acceptor PZ1 by embedding an acceptor-donor-acceptor building block into the polymer main chain and showing a record-high PCE for the all-PSCs is demonstrated.
Abstract: All-polymer solar cells (all-PSCs) offer unique morphology stability for the application as flexible devices, but the lack of high-performance polymer acceptors limits their power conversion efficiency (PCE) to a value lower than those of the PSCs based on fullerene derivative or organic small molecule acceptors. We herein demonstrate a strategy to synthesize a high-performance polymer acceptor PZ1 by embedding an acceptor–donor–acceptor building block into the polymer main chain. PZ1 possesses broad absorption with a low band gap of 1.55 eV and high absorption coefficient (1.3×105 cm−1). The all-PSCs with the wide-band-gap polymer PBDB-T as donor and PZ1 as acceptor showed a record-high PCE of 9.19 % for the all-PSCs. The success of our polymerization strategy can provide a new way to develop efficient polymer acceptors for all-PSCs.
417 citations
TL;DR: Wang et al. as discussed by the authors constructed superstrate Sb2Se3 solar cells with a certified power conversion efficiency of 5.93% using random oriented ZnO produced by spray pyrolysis.
Abstract: Sb2Se3, a binary compound containing non-toxic and Earth-abundant constituents, is a promising absorber material for low-cost, high-efficiency photovoltaics. Current Sb2Se3 thin-film solar cells use toxic CdS as the buffer layer and suffer from unsatisfactory stability. Here we selected ZnO as the buffer layer and constructed superstrate Sb2Se3 solar cells with a certified power conversion efficiency of 5.93%. Randomly oriented ZnO produced by spray pyrolysis induced the growth of Sb2Se3 with preferred [221] orientation, and hence resulted in devices with fewer interfacial defects and better efficiency. Moreover, our unencapsulated device survived the stringent damp-heat (85 ∘C, 85% humidity, 1,100 h), light-soaking (50 ∘C, 1.3 sun, 1,100 h), thermal cycling, and ultraviolet preconditioning tests. The combined features of stability, Earth-abundant constituent and potentially low-cost manufacturing highlight the great potential of Sb2Se3 solar cell as a possible non-toxic alternative to CdTe photovoltaics. Thin-film photovoltaic devices are often based on toxic or rare materials. Here, Wang et al. grow oriented Sb2Se3 thin film on a ZnO buffer layer, and fabricate solar cells with a certified 5.9% conversion efficiency and which pass harsh stability tests under humidity, heat and illumination.
413 citations
TL;DR: Five polymer donors with distinct chemical structures and different electronic properties are surveyed in a planar and narrow-bandgap fused-ring electron acceptor (IDIC)-based organic solar cells, which exhibit power conversion efficiencies of up to 11%.
Abstract: Five polymer donors with distinct chemical structures and different electronic properties are surveyed in a planar and narrow-bandgap fused-ring electron acceptor (IDIC)-based organic solar cells, which exhibit power conversion efficiencies of up to 11%.
379 citations
TL;DR: Ternary polymer solar cells are fabricated based on one donor PBDB-T and two acceptors (a methyl-modified small-molecular acceptor and a bis-adduct of Bis[70]PCBM) and a high power conversion efficiency can be achieved.
Abstract: Ternary polymer solar cells are fabricated based on one donor PBDB-T and two acceptors (a methyl-modified small-molecular acceptor (IT-M) and a bis-adduct of Bis[70]PCBM). A high power conversion efficiency of 12.2% can be achieved. The photovoltaic performance of the ternary polymer solar cells is not sensitive to the composition of the blend.
357 citations
TL;DR: In this paper, the synergistic effects of processing solvents and molecular weight on the photovoltaic performance of all-polymer solar cells were investigated, which consist of an n-type polymer N2200 and a p-type wide bandgap polymer PTzBI that are made of benzodithiophene and imide-functionalized benzotriazole units.
Abstract: Increasing interest has been devoted to developing high-performance all-polymer solar cells (all-PSCs) owing to their specific advantages in light absorption and long-term stability. In this work, we systematically investigated the synergistic effects of processing solvents and molecular weight on the photovoltaic performance of all-PSCs, which consist of an n-type polymer N2200 and a p-type wide bandgap polymer PTzBI that are made up of benzodithiophene and imide-functionalized benzotriazole units. It is noted that increasing the molecular weight of N2200 can simultaneously enhance exciton generation and dissociation, reduce bimolecular recombination, and facilitate charge extraction. The films processed with the environmentally-friendly solvent 2-methyl-tetrahydrofuran (MeTHF) exhibit a more favourable film morphology than those processed with commonly used halogenated solvents. The all-PSC consisting of the high molecular weight N2200 and PTzBI processed with the environmentally friendly solvent MeTHF presents a remarkable power conversion efficiency of 9.16%, which is the highest value so far observed for all-PSCs. Of particular interest is that the PCE remains 6.37% with the active layer thickness of 230 nm. These observations imply the great promise of the developed all-PSCs for practical applications toward high-throughput roll-to-roll technology.
323 citations
TL;DR: The morphology characterizations show that both the polymer and the SMA can maintain high crystallinity in the blend film, resulting in crystalline and small domains, which is the best performance for a non-fullerene organic solar cell with such a small voltage loss.
Abstract: To achieve efficient non-fullerene organic solar cells, it is important to reduce the voltage loss from the optical bandgap to the open-circuit voltage of the cell. Here we report a highly efficient non-fullerene organic solar cell with a high open-circuit voltage of 1.08 V and a small voltage loss of 0.55 V. The high performance was enabled by a novel wide-bandgap (2.05 eV) donor polymer paired with a narrow-bandgap (1.63 eV) small-molecular acceptor (SMA). Our morphology characterizations show that both the polymer and the SMA can maintain high crystallinity in the blend film, resulting in crystalline and small domains. As a result, our non-fullerene organic solar cells realize an efficiency of 11.6%, which is the best performance for a non-fullerene organic solar cell with such a small voltage loss.
TL;DR: A novel wide-bandgap conjugated copolymer based on an imide-functionalized benzotriazole building block containing a siloxane-terminated side-chain is developed and can be a promising candidate toward high-performance all-PSCs for practical applications.
Abstract: A novel wide-bandgap conjugated copolymer based on an imide-functionalized benzotriazole building block containing a siloxane-terminated side-chain is developed. This copolymer is successfully used to fabricate highly efficient all-polymer solar cells (all-PSCs) processed at room temperature with the green-solvent 2-methyl-tetrahydrofuran. When paired with a naphthalene diimide-based polymer electron-acceptor, the all-PSC exhibits a maximum power conversion efficiency (PCE) of 10.1%, which is the highest value so far reported for an all-PSC. Of particular interest is that the PCE remains 9.4% after thermal annealing at 80 °C for 24 h. The resulting high efficiency is attributed to a combination of high and balanced bulky charge carrier mobility, favorable face-on orientation, and high crystallinity. These observations indicate that the resulting copolymer can be a promising candidate toward high-performance all-PSCs for practical applications.
TL;DR: Fullerene-free organic solar cells show over 11% power conversion efficiency, processed by low toxic solvents, and the applied donor and acceptor in the bulk heterojunction exhibit almost the same highest occupied molecular orbital level, yet exhibit very efficient charge creation.
Abstract: Fullerene-free organic solar cells show over 11% power conversion efficiency, processed by low toxic solvents. The applied donor and acceptor in the bulk heterojunction exhibit almost the same highest occupied molecular orbital level, yet exhibit very efficient charge creation.
TL;DR: The results indicate that fluorobenzotriazole based 2D conjugated p-OSs are promising medium bandgap donors in the nonfullerene OSCs.
Abstract: In the last two years, polymer solar cells (PSCs) developed quickly with n-type organic semiconductor (n-OSs) as acceptor. In contrast, the research progress of nonfullerene organic solar cells (OSCs) with organic small molecule as donor and the n-OS as acceptor lags behind. Here, we synthesized a D–A structured medium bandgap organic small molecule H11 with bithienyl-benzodithiophene (BDTT) as central donor unit and fluorobenzotriazole as acceptor unit, and achieved a power conversion efficiency (PCE) of 9.73% for the all organic small molecules OSCs with H11 as donor and a low bandgap n-OS IDIC as acceptor. A control molecule H12 without thiophene conjugated side chains on the BDT unit was also synthesized for investigating the effect of the thiophene conjugated side chains on the photovoltaic performance of the p-type organic semiconductors (p-OSs). Compared with H12, the 2D-conjugated H11 with thiophene conjugated side chains shows intense absorption, low-lying HOMO energy level, higher hole mobility ...
TL;DR: An abnormal strong burn-in degradation in highly efficient polymer solar cells is demonstrated caused by spinodal demixing of the donor and acceptor phases, which dramatically reduces charge generation and can be attributed to the inherently low miscibility of both materials.
Abstract: The performance of organic solar cells is determined by the delicate, meticulously optimized bulk-heterojunction microstructure, which consists of finely mixed and relatively separated donor/acceptor regions. Here we demonstrate an abnormal strong burn-in degradation in highly efficient polymer solar cells caused by spinodal demixing of the donor and acceptor phases, which dramatically reduces charge generation and can be attributed to the inherently low miscibility of both materials. Even though the microstructure can be kinetically tuned for achieving high-performance, the inherently low miscibility of donor and acceptor leads to spontaneous phase separation in the solid state, even at room temperature and in the dark. A theoretical calculation of the molecular parameters and construction of the spinodal phase diagrams highlight molecular incompatibilities between the donor and acceptor as a dominant mechanism for burn-in degradation, which is to date the major short-time loss reducing the performance and stability of organic solar cells.
TL;DR: With this polymer acceptor, a new record power-conversion efficiencies (PCE) of 8.59% has been achieved for all-PSCs and the stronger absorption of NDP-V in the shorter-wavelength range offers a better complement to the donor.
Abstract: A new polymer acceptor, naphthodiperylenetetraimide-vinylene (NDP-V), featuring a backbone of altenating naphthodiperylenetetraimide and vinylene units is designed and applied in all-polymer solar cells (all-PSCs). With this polymer acceptor, a new record power-conversion efficiencies (PCE) of 8.59% has been achieved for all-PSCs. The design principle of NDP-V is to reduce the conformational disorder in the backbone of a previously developed high-performance acceptor, PDI-V, a perylenediimide-vinylene polymer. The chemical modifications result in favorable changes to the molecular packing behaviors of the acceptor and improved morphology of the donor-acceptor (PTB7-Th:NDP-V) blend, which is evidenced by the enhanced hole and electron transport abilities of the active layer. Moreover, the stronger absorption of NDP-V in the shorter-wavelength range offers a better complement to the donor. All these factors contribute to a short-circuit current density (J sc ) of 17.07 mA cm-2 . With a fill factor (FF) of 0.67, an average PCE of 8.48% is obtained, representing the highest value thus far reported for all-PSCs.
TL;DR: In this article, the progress in lowbandgap conjugated polymers and several tandem OPV cells enabled by these low-bandgap polymers is discussed. But the authors focus on the progress of polymer-based organic photovoltaic (OPV).
Abstract: The technology of polymer-based organic photovoltaic (OPV) cells has made great progress in the past decade, with the power conversion efficiency increasing from just a few per cent to around 12%, and the stability increasing from hours to years. One of the important milestones in this progress has been the invention of infrared-absorbing low-bandgap polymers, which allows the OPV cells to form effective tandem structures for harvesting near-infrared energy from the solar spectrum. In this Review, we focus on the progress in low-bandgap conjugated polymers and several tandem OPV cells enabled by these low-bandgap polymers. Specifically, we cover polymer-based tandem solar cells; hybrid tandem solar cells combining polymers with hydrogenated amorphous silicon; and unconventional solar cells. For each of these technologies, we address the challenges and offer our perspectives for future development. Low-bandgap (<1.6 eV) polymers enable polymer solar cells to form effective tandem structures for harvesting near-infrared solar energy as well as reducing thermal loss. This Review summarizes recent progress and provides a perspective on various low-bandgap polymer-containing tandem solar cells; namely, pure polymer–polymer tandem, hybrid polymer–amorphous silicon tandem and unconventional perovskite–polymer tandem solar cells.
TL;DR: The effect of fluorination on the device performance of solar cells as a function of the position of fluorine (on the acceptor unit or on the donor unit) is examined, aiming to outline a clear understanding of the benefits of this curious substituent.
Abstract: ConspectusOrganic solar cells (OSCs) have been a rising star in the field of renewable energy since the introduction of the bulk heterojunction (BHJ) in 1992. Recent advances have pushed the efficiencies of OSCs to over 13%, an impressive accomplishment via collaborative efforts in rational materials design and synthesis, careful device engineering, and fundamental understanding of device physics. Throughout these endeavors, several design principles for the conjugated donor polymers used in such solar cells have emerged, including optimizing the conjugated backbone with judicious selection of building blocks, side-chain engineering, and substituents. Among all of the substituents, fluorine is probably the most popular one; improved device characteristics with fluorination have frequently been reported for a wide range of conjugated polymers, in particular, donor–acceptor (D–A)-type polymers. Herein we examine the effect of fluorination on the device performance of solar cells as a function of the positio...
TL;DR: The results demonstrate that side-chain conjugation can tune energy levels, enhance absorption, and electron mobility, and finally enhance photovoltaic performance of nonfullerene acceptors.
Abstract: A side-chain conjugation strategy in the design of nonfullerene electron acceptors is proposed, with the design and synthesis of a side-chain-conjugated acceptor (ITIC2) based on a 4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b′]di(cyclopenta-dithiophene) electron-donating core and 1,1-dicyanomethylene-3-indanone electron-withdrawing end groups. ITIC2 with the conjugated side chains exhibits an absorption peak at 714 nm, which redshifts 12 nm relative to ITIC1. The absorption extinction coefficient of ITIC2 is 2.7 × 105m−1 cm−1, higher than that of ITIC1 (1.5 × 105m−1 cm−1). ITIC2 exhibits slightly higher highest occupied molecular orbital (HOMO) (−5.43 eV) and lowest unoccupied molecular orbital (LUMO) (−3.80 eV) energy levels relative to ITIC1 (HOMO: −5.48 eV; LUMO: −3.84 eV), and higher electron mobility (1.3 × 10−3 cm2 V−1 s−1) than that of ITIC1 (9.6 × 10−4 cm2 V−1 s−1). The power conversion efficiency of ITIC2-based organic solar cells is 11.0%, much higher than that of ITIC1-based control devices (8.54%). Our results demonstrate that side-chain conjugation can tune energy levels, enhance absorption, and electron mobility, and finally enhance photovoltaic performance of nonfullerene acceptors.
01 Jul 2017
TL;DR: In this article, the phase stability of cubic cubic CsPbI3 perovskite is investigated for single junction or tandem solar cells due to their large bandgaps.
Abstract: Hygroscopicity risk and organic–inorganic hybrid perovskites easy decomposition in solar cells limit their usefulness. Apart from the hybrid organic–inorganic perovskites, inorganic perovskite solar cells display a better stability toward moisture, light soaking, and thermal stressing. However, most inorganic perovskites are inappropriate for single junction or tandem solar cells due to their large bandgaps (>1.8 eV), which eventually results in light absorption loss. Fortunately, cubic CsPbI3 perovskite (having 1.73 eV bandgap) could potentially serve as top cells in tandem devices with silicon solar cells. Poor phase stability of CsPbI3 is considered a major obstacle to design CsPbI3 perovskite solar cells. This review highlights the most recent studies on the progress in CsPbI3-based solar cell device field. Moreover, this review also summarizes certain strategies to improve phase stability, such as size reduction to nanocrystal or external cations/anions doping, with the aim to improve the devices design.
TL;DR: A new, easy, and efficient approach is reported to enhance the driving force for charge transfer, break tradeoff between open-circuit voltage and shortcircuit current, and simultaneously achieve very small energy loss, very high open-Circuit voltage, and very high efficiency in fullerene-free organic solar cells via an energy driver.
Abstract: A new, easy, and efficient approach is reported to enhance the driving force for charge transfer, break tradeoff between open-circuit voltage and short-circuit current, and simultaneously achieve very small energy loss (0.55 eV), very high open-circuit voltage (>1 V), and very high efficiency (>10%) in fullerene-free organic solar cells via an energy driver.
TL;DR: In this paper, the authors discussed the present development in fullerene derivative and summarized the efficient Fullerene derivatives for the BHJ-OSCs application suggest a possible application for the future cage-based solar cells.
TL;DR: In this article, a doctor-bladed OIHP solar cell with p-i-n planar hetero-junction structure was used to enhance the power conversion efficiency.
Abstract: Organic-inorganic halide perovskite (OIHP) solar cells with efficiency over 18% power conversion efficiency (PCE) have been widely achieved with lab scale spin-coating method which is however not scalable for the fabrication of large area solar panels. The PCEs of OIHP solar cells made by scalable deposition methods, such as doctor-blading or slot-die coating, have been lagging far behind than spin-coated devices. In this study the authors report composition engineering in doctor-bladed OIHP solar cells with p-i-n planar hetero-junction structure to enhance their efficiency. Phase purer OIHP thin films are obtained by incorporating a small amount of cesium (Cs+) and bromine (Br-) ions into perovskite precursor solution, which also reduces the required film formation temperature. Pinhole free OIHP thin films with micrometer-sized grains have been obtained assisted by a secondary grain growth with added methylammonium chloride into the precursor solution. The OIHP solar cells using these bladed thin films achieved PCEs over 19.0%, with the best stabilized PCE reaching 19.3%. This represents a significant step toward scalable manufacture of OIHP solar cells.
TL;DR: A novel-small molecular acceptor with electron-deficient 1,3,5-triazine as the core and perylene diimides as the arms is developed as the acceptor material for efficient bulk heterojunction organic solar cells with an efficiency of 9.15%.
Abstract: A novel-small molecular acceptor with electron-deficient 1,3,5-triazine as the core and perylene diimides as the arms is developed as the acceptor material for efficient bulk heterojunction organic solar cells with an efficiency of 9.15%.
TL;DR: E enlarging the conjugated area of the terminal-group in these A-D-A-type SMAs is a promising approach not only for enhancing the electron mobility, but also for improving the blend morphology, and both of them are conducive to the fill-factor breakthrough.
Abstract: Improving the fill factor (FF) is known as a challenging issue in organic solar cells (OSCs). Herein, a strategy of extending the conjugated area of end-group is proposed for the molecular design of acceptor-donor-acceptor (A-D-A)-type small molecule acceptor (SMA), and an indaceno[1,2-b:5,6-b']dithiophene-based SMA, namely IDTN, by end-capping with the naphthyl fused 2-(3-oxocyclopentylidene)malononitrile is synthesized. Benefiting from the π-conjugation extension by fusing two phenyls, IDTN shows stronger molecular aggregation, more ordered packing structure, thus over one order of magnitude higher electron mobility relative to its counterpart. By utilizing the fluorinated polymer (PBDB-TF) as the electron donor, the corresponding device exhibits a high efficiency of 12.2% with a record-high FF of 0.78, which is approaching the theoretical limit of OSCs. Compared with the reference molecule, such a high FF in the IDTN system can be mainly attributed to the more ordered π-π packing of acceptor aggregates, higher domain purity and symmetric carrier transport in the blend. Hence, enlarging the conjugated area of the terminal-group in these A-D-A-type SMAs is a promising approach not only for enhancing the electron mobility, but also for improving the blend morphology, and both of them are conducive to the fill-factor breakthrough.
TL;DR: In this article, a materials design concept for achieving large-area, solution-coated all-polymer bulk heterojunction solar cells with stable phase separation morphology between the donor and acceptor is presented.
Abstract: The challenge of continuous printing in high-efficiency large-area organic solar cells is a key limiting factor for their widespread adoption. A materials design concept for achieving large-area, solution-coated all-polymer bulk heterojunction solar cells with stable phase separation morphology between the donor and acceptor is presented. The key concept lies in inhibiting strong crystallization of donor and acceptor polymers, thus forming intermixed, low crystallinity, and mostly amorphous blends. Based on experiments using donors and acceptors with different degree of crystallinity, the results show that microphase separated donor and acceptor domain sizes are inversely proportional to the crystallinity of the conjugated polymers. This methodology of using low crystallinity donors and acceptors has the added benefit of forming a consistent and robust morphology that is insensitive to different processing conditions, allowing one to easily scale up the printing process from a small-scale solution shearing coater to a large-scale continuous roll-to-roll (R2R) printer. Large-area all-polymer solar cells are continuously roll-to-roll slot die printed with power conversion efficiencies of 5%, with combined cell area up to 10 cm2. This is among the highest efficiencies realized with R2R-coated active layer organic materials on flexible substrate.
TL;DR: In this work, highly efficient ternary-blend organic solar cells (TB-OSCs) are reported based on a low-bandgap copolymer of PTB7-Th, a medium-band gap copolymers of PBDB-T, and a wide- bandgap small molecule of SFBRCN, which exhibit a broad composition tolerance with a high PCE over 10% throughout the whole blend ratios.
Abstract: In this work, highly efficient ternary-blend organic solar cells (TB-OSCs) are reported based on a low-bandgap copolymer of PTB7-Th, a medium-bandgap copolymer of PBDB-T, and a wide-bandgap small molecule of SFBRCN. The ternary-blend layer exhibits a good complementary absorption in the range of 300–800 nm, in which PTB7-Th and PBDB-T have excellent miscibility with each other and a desirable phase separation with SFBRCN. In such devices, there exist multiple energy transfer pathways from PBDB-T to PTB7-Th, and from SFBRCN to the above two polymer donors. The hole-back transfer from PTB7-Th to PBDB-T and multiple electron transfers between the acceptor and the donor materials are also observed for elevating the whole device performance. After systematically optimizing the weight ratio of PBDB-T:PTB7-Th:SFBRCN, a champion power conversion efficiency (PCE) of 12.27% is finally achieved with an open-circuit voltage (Voc) of 0.93 V, a short-circuit current density (Jsc) of 17.86 mA cm−2, and a fill factor of 73.9%, which is the highest value for the ternary OSCs reported so far. Importantly, the TB-OSCs exhibit a broad composition tolerance with a high PCE over 10% throughout the whole blend ratios.
TL;DR: It is demonstrated difluoro-substitution of thiophene conjugated side chain on donor polymer can suppress triplet formation for reducing carrier recombination and indicates that side chain engineering can provide a new solution to suppress carrier recombinations toward high efficiency.
Abstract: Suppression of carrier recombination is critically important in realizing high-efficiency polymer solar cells. Herein, it is demonstrated difluoro-substitution of thiophene conjugated side chain on donor polymer can suppress triplet formation for reducing carrier recombination. A new medium bandgap 2D-conjugated D-A copolymer J91 is designed and synthesized with bi(alkyl-difluorothienyl)-benzodithiophene as donor unit and fluorobenzotriazole as acceptor unit, for taking the advantages of the synergistic fluorination on the backbone and thiophene side chain. J91 demonstrates enhanced absorption, low-lying highest occupied molecular orbital energy level, and higher hole mobility, in comparison with its control polymer J52 without fluorination on the thiophene side chains. The transient absorption spectra indicate that J91 can suppress the triplet formation in its blend film with n-type organic semiconductor acceptor m-ITIC (3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone)-5,5,11,11-tetrakis(3-hexylphenyl)-dithieno[2,3-d:2,3'-d']-s-indaceno[1,2-b:5,6-b']-dithiophene). With these favorable properties, a higher power conversion efficiency of 11.63% with high VOC of 0.984 V and high JSC of 18.03 mA cm-2 is obtained for the polymer solar cells based on J91/m-ITIC with thermal annealing. The improved photovoltaic performance by thermal annealing is explained from the morphology change upon thermal annealing as revealed by photoinduced force microscopy. The results indicate that side chain engineering can provide a new solution to suppress carrier recombination toward high efficiency, thus deserves further attention.
TL;DR: In this paper, the authors summarized the progress in the understanding of the function of fullerenes in perovskite solar cells in blocking leakage through pin-holes, passivating the defects at the pervskite film surfaces and grain boundaries, and modulating the open-circuit voltage of the devices.
Abstract: There is increasing interest in the application of fullerene-based carbon materials in perovskite solar cells for increased efficiency, reduced hysteresis, and improved stability. This Perspective summarizes the progress in the understanding of the function of fullerenes in perovskite solar cells in blocking leakage through pin-holes, passivating the defects at the perovskite film surfaces and grain boundaries, and modulating the open-circuit voltage of the devices. We also critically reviewed several open questions on the functions of fullerenes in perovskite solar cells based mainly on recent progress: How do fullerenes reduce current hysteresis? What is the function of double-fullerene layers? Does the doping of the fullerene by perovskite contribute to eliminating the photocurrent hysteresis at room temperature? Why do some perovskite/fullerene solar cells still have hysteresis at low temperature? Are perovskite solar cells with fullerenes in the intergranular boundaries bulk heterojunction solar cell...
TL;DR: This work demonstrates the potential of (CH3NH3)3Bi2I9 for highly efficient and long-term stable solar cells, which are characterized with absorption coefficient, trap density of states, and charge diffusion length comparable to those of some lead perovskite analogues.
Abstract: Bismuth-based solar cells have exhibited some advantages over lead perovskite solar cells for nontoxicity and superior stability, which are currently two main concerns in the photovoltaic community. As for the perovskite-related compound (CH3NH3)3Bi2I9 applied for solar cells, the conversion efficiency is severely restricted by the unsatisfactory photoactive film quality. Herein we report a novel two-step approach— high-vacuum BiI3 deposition and low-vacuum homogeneous transformation of BiI3 to (CH3NH3)3Bi2I9—for highly compact, pinhole-free, large-grained films, which are characterized with absorption coefficient, trap density of states, and charge diffusion length comparable to those of some lead perovskite analogues. Accordingly, the solar cells have realized a record power conversion of efficiency of 1.64% and also a high external quantum efficiency approaching 60%. Our work demonstrates the potential of (CH3NH3)3Bi2I9 for highly efficient and long-term stable solar cells.