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Efficiency Enhancement of Hybrid Perovskite Solar Cells with MEH-PPV Hole-Transporting Layers


In this study, hybrid perovskite solar cells are fabricated using poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) and poly(3-hexylthiophene-2,5-diyl) (P3HT) as dopant-free hole-transporting materials (HTMs) and two solution processes (one- and two-step methods, respectively) for preparing methylammonium lead iodide perovskite. By optimizing the concentrations and solvents of MEH-PPV solutions, a power conversion efficiency of 9.65% with hysteresis-less performance is achieved, while the device with 2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′spirobifluorene (Spiro-OMeTAD) doped with lithium salts and tert-butylpyridine (TBP) exhibits an efficiency of 13.38%. This result shows that non-doped MEH-PPV is a suitable, low-cost HTM for efficient polymer-based perovskite solar cells. The effect of different morphologies of methylammonium lead iodide perovskite on conversion efficiency is also investigated by incident photon-to-electron conversion efficiency (IPCE) curves and electrochemical impedance spectroscopy (EIS).


In recent years, hybrid organolead halide perovskite solar cells have attracted significant attention, attributed to their inherent facile fabrication, potential cost-effectiveness and high power conversion efficiency (PCE) reaching ~20%1,2,3,4,5. In 2009, Miyasaka et al. first reported a solar cell incorporating a perovskite absorber and this perovskite-sensitized solar cell containing a liquid electrolyte exhibits a conversion efficiency of 3.8%6. In 2011, Park et al. reported a further increase in the conversion efficiency to 6.5%7. However, because the liquid electrolyte is corrosive, the perovskite material dissolves within a few minutes of device operation; this prompts a shift towards solid-state devices consisting of hole conductors such as 2,2′,7,7′-tetrakis(N, N-di-p-methoxyphenylamine)-9,9′spirobifluorene (Spiro-OMeTAD)1, poly(3-hexylthiophene-2,5-diyl) (P3HT)8,9, poly-(2,1,3-benzothiadiazole-4,7-diyl(4,4-bis(2-ethylhexyl)-4H-cyclopenta)2,1-b:3,4-b′)dithiophene-2,6-diyl)) (PCPDTBT)10 and poly-triarylamine (PTAA)4,10 and other hole-transporting materials (HTMs)11,12,13,14,15,16. Spiro-OMeTAD is the most commonly used HTM, which exhibits efficient charge transport, low recombination rates and good pore filling of the TiO2 layer; these characteristics enhance device performance with respect to polymer-based HTMs17,18. As a small-molecule HTM, pristine Spiro-OMeTAD exhibits low mobility (approximately 10−6 to 10−5 cm2 V−1s−1)19,20. The hole conductivity of a Spiro-OMeTAD film has been reported to be improved significantly by an order of magnitude through doping with a cobalt electrolyte and lithium salts under air oxidation21,22,23,24,25. Nevertheless, precise control of these poorly defined oxidative processes is challenging, due to the lack of physical understanding and device reproducibility. Additionally, oxidation-induced efficiency enhancements decline after the devices are encapsulated/stored under inert atmosphere, thus preventing from the real applications26. Furthermore, some dopants are hydrophilic, which compromises solar cell stability considering that the perovskite active layers are susceptible to moisture-induced degradation27. Consequently, developing dopant-free, hydrophobic/O2-stable HTMs is critical for advancing perovskite solar cell technologies28. However, for a conducting polymer, van der Waals interactions between polymer chains (as well as those between polymer and solvent molecules in solution-processed films) are generally thought to determine the manner in which the chains are packed in the film state29. In fact, the film morphology developed during processing significantly affects inter-chain hopping and device performance. Besides, the size of the polymeric chain can reduce the pore filling of the mesoporous layer, thereby limiting conversion efficiency30. Some studies have demonstrated that the electronic properties of conjugated polymers possibly depend on film processing conditions, such as solvent, solution concentration, additives and methods or conditions of film preparation31.

In this study, poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV) is demonstrated to be a suitable HTM for efficient perovskite-based solar cells. A fluorine-doped tin oxide (FTO) substrate/TiO2/CH3NH3PbI3/MEH-PPV/Au architecture is proposed with the aim of optimizing the performance of MEH-PPV-based perovskite solar cells by controlling the solvents and solution concentration. Although Masi et al. have reported an MEH-PPV with perovskite for fabricating an optoelectronic device with polymer or perovskite nanocomposites32, which exhibits an inferior efficiency of 3%, the structure of the devices in their study is significantly different from those fabricated herein. Their device structure is similar to that of the bulk hetero-junction solar cells by exploiting polymers as the template agent and forming perovskite inside the polymer matrix as the nanocomposite film, which is obtained from a MEH-PPV, methylammonium iodide and lead iodide blend solution in a binary mixture of solvents tetrahydrofurane (THF) and N,N-dimethylformamide (DMF)32. For the first time, the combination of dopant-free MEH-PPV and CH3NH3PbI3 is used in the present study, attaining a final device efficiency of 9.65%; to the best of our knowledge, this efficiency is the highest reported value for a solar cell using MEH-PPV as an HTM.


Perovskite solar cells with different HTMs were fabricated under ambient air conditions; details are described in methods part. Figure 1 shows the energy band diagram and chemical structures of MEH-PPV, P3HT and Spiro-OMeTAD. For devices of the type FTO/TiO2/perovskite/HTMs/Au, the open-circuit voltage (VOC) under illumination of 1 sun is determined by the difference between the TiO2 quasi-Fermi energy level of ~3.2 eV and the work function of the Au electrode or the HOMO level of the HTMs. In our system, the Au electrode work function of −5.1 eV forms a nearly Ohmic contact with the HOMO level of HTMs −5.4 to −5.1 eV. The HOMO levels of polymer-based MEH-PPV and P3HT were slightly lower than that of Spiro-OMeTAD, indicating that VOC is possibly higher in these two HTMs. Figure 2 shows the cross-sectional scanning electron microscopy (SEM) images of the layers observed for the perovskite solar cells fabricated by the one-step method (CH3NH3PbI3−xClx) and two-step method (CH3NH3PbI3) (tetragonal structure) using Spiro-OMeTAD and MEH-PPV as the HTMs. The polymer-based MEH-PPV layer (Fig. 2c,f,g) exhibited morphologies significantly different from those of the small-molecular-based Spiro-OMeTAD layer (Fig. 2a,b,d,e). As compared to the MEH-PPV layer, the Spiro-OMeTAD layer was significantly more smooth and compact, attributed to the small molecular property. Besides, both Spiro-OMeTAD (Fig. 2a) and MEH-PPV (10 mg mL−1) layers (Fig. 2c) with thicknesses of approximately 350 nm completely covered the perovskite/TiO2 layers; however, a lower MEH-PPV concentration (5 mg mL−1) resulted in a thinner layer (Fig. 2f). In a typical one-step method, a mesoporous TiO2 nanocrystal layer was deposited above a TiO2 compact layer pre-deposited on a ~300 nm thick FTO, followed by spin-coating with an organo-lead halide perovskite precursor solution (CH3NH3I and PbCl2 in DMF); the spin-coated perovskite/TiO2 layer was dried at 100 °C (Fig. 2a). However, in the two-step method, lead iodide (PbI2) was first introduced into the TiO2 nanopores by spin-coating a 1 M solution of PbI2 in DMF, followed by drying at 70 °C. Subsequently, the TiO2/PbI2 composite film was dipped into a solution of CH3NH3I in 2-propanol (10 mg mL−1) and the color immediately changed from yellow to dark brown, indicating the formation of CH3NH3PbI3. From Fig. 2b, e, the two-step method resulted in the formation of a capping layer with a tetragonal structure significantly different from that produced by the one-step method. The perovskite tetragonal crystals were significantly greater than the TiO2 nanoparticles (~400 nm); hence, perovskite is not a thin conformal layer covering the TiO2 particles sandwiched by Spiro-OMeTAD. As can be observed in Fig. 2e, the TiO2 pores were filled with PbI2 and a capping layer of PbI2 was also formed during the first coating step. During the second step in which the TiO2/PbI2 composed film was dipped into a CH3NH3I solution, PbI2 was completely converted to perovskite, as confirmed by X-ray diffraction (XRD) (Figure S1 in the Supplementary Information). Hence, perovskite forms not only inside the TiO2 pores but also on the surface of the TiO2 layer. Because the TiO2 film has a small pore size, the growth of perovskite is limited inside the mesopores; however, larger crystal growth is possible on the top of the TiO2 film.

Figure 1

Energy band diagram and molecular structures of MEH-PPV, P3HT and Spiro-OMeTAD.

Figure 2

Cross-sectional SEM images of the layers observed in perovskite solar cells fabricated by the (a,d) one-step method of preparing CH3NH3PbI3−xClx and (b,e) two-step method of preparing CH3NH3PbI3 (tetragonal structure) with Spiro-OMeTAD (15 mg mL−1), (c,g) MEH-PPV (10 mg mL−1) and (f) MEH-PPV (5 mg mL−1).

The effects of solvents and concentration on device performance are investigated. Figure 3 shows the typical current density–voltage characteristics (J–V) measured under 100 mW cm−2 AM 1.5 solar illumination for solar cells with HTMs of 8 wt% Spiro-OMeTAD in chlorobenzene (CB), 15 mg mL−1 P3HT in CB and 5–15 mg mL−1 MEH-PPV in CB, dichlorobenzene (DCB) and toluene. Table 1 summarizes the values of the device parameters, such as short-circuit current density (JSC), VOC, fill factor (FF) and PCE (η) values and both the one- and two-step methods for preparing the perovskite layer were tested. However, because the one-step method demonstrates more general applicability in this work, it is used for preparing the perovskite layer; it was systematically investigated to examine the effect of solvents on the use of Spiro-OMeTAD, P3HT and MEH-PPV based on one-step method. We also prepared the devices based on the planar structure (without any mesoporous TiO2 layer) by the one-step method, as shown in Figure S2 in the Supplementary Information. Since the planar structure one always comes with a huge hysteresis, we decided to use the devices structure with a mesoporous TiO2 layer. The effect of the HTM thickness of MEH-PPV (Fig. 2f,g) was examined by controlling the variation of the CB concentration. PPV was insoluble in most solvents as its backbone comprises rigid monomer units; however, its derivative, hairy-rod polymer MEH-PPV, was highly soluble in common organic solvents, such as THF, chloroform, chlorobenzene, dichlorobenzene, toluene and xylene as its backbone comprises short flexible soft side chains33. Nevertheless, at a MEH-PPV concentration of higher than 15 mg mL−1, the viscosity of the MEH-PPV solution became so high that it was difficult to spread its solution on perovskite so as to achieve a completely covered layer. In the MEH-PPV/toluene solution, toluene molecules are among the conjugated main chains and they prevent segment aggregation from the inter-conjugated main chains. Previously, some studies have demonstrated that the charge carrier mobility in toluene-cast MEH-PPV films is higher than that of CB-cast MEH-PPV films34,35. The MEH-PPV/toluene-based device with an optimized thickness or concentration at 10 mg mL−1 exhibited the highest η of 8.87%. The low VOC for Spiro-OMeTAD can be explained by the fact that Spiro-OMeTAD (−5.1 eV) has a HOMO higher than that of MEH-PPV (−5.4 eV) (Fig. 1). As for the hysteresis behavior of J–V performance, MEH-PPV-based cells exhibited good hysteresis-free J–V characteristics, while P3HT-based cells and Spiro-OMeTAD cells exhibited small hysteresis between forward and back scans (Fig. 4).

Table 1 Photovoltaic characteristics, JSC, VOC, FF and η of perovskite solar cells with Spiro-OMeTAD, P3HT and MEH-PPV as HTMs dissolved in various solvents as well as concentrations.
Figure 3

Current density–voltage (J–V) characteristic curves of perovskite solar cells with Spiro-OMeTAD, P3HT and MEH-PPV HTMs dissolved in various solvents as well as concentrations.

Figure 4

Current density–voltage (J–V) characteristic curves of the perovskite solar cells with Spiro-OMeTAD, P3HT and MEH-PPV HTMs at forward scan (FS) and backward scan (BS).

For further enhancing device performance, the two-step method for preparing the perovskite layer was utilized, including post-treatment of the mesoporous TiO2 layer using TiCl4 before the deposition of the perovskite layer. In a dye-sensitized solar cell (DSSC) system, TiCl4 post-treatment improves the adhesion and mechanical strength of the nanocrystalline TiO2 layer and enhances the surface roughness factor and necking of the TiO2 particles, thereby increasing dye adsorption and resulting in high photocurrent36. Figure 5 and Table 2 show the J–V curves, histogram with the Gaussian fit of PCE distribution and photovoltaic characteristics of perovskite solar cells fabricated using Spiro-OMeTAD and MEH-PPV as the HTMs by one- and two-step methods for preparing the perovskite layer with or without post-treatment using TiCl4. From the results, JSC and VOC significantly increased after post-treatment of the mesoporous TiO2 layer using TiCl4 for Spiro-OMeTAD; this increase in VOC and JSC is attributed to the blocking of recombination at the interface between perovskite and the FTO interface and post-treatment using TiCl4, respectively. The best performance for MEH-PPV-based devices was observed after fabrication by the one-step method for preparing the perovskite layer with post-treatment of the mesoporous TiO2 layer using TiCl4 with a η of 9.65%. The devices fabricated by the one-step method always exhibited high JSC, while devices fabricated by the two-step method always exhibited high VOC compared to each other in both methods. This result is attributed to either the difference in the morphologies of perovskite observed between the one- and two-step methods or the incorporation of Cl residues in the perovskite crystals. The best performance for the Spiro-OMeTAD-based HTMs was observed by the two-step method for preparing the perovskite layer with post-treatment of the mesoporous TiO2 layer using TiCl4, achieving an η of 13.38%, a JSC of 21.19 mA cm−2, a VOC of 1.04 V and an FF of 0.61 (backward scan), albeit with presence of small hysteresis.

Table 2 Photovoltaic characteristics, JSC, VOC, FF and η of perovskite solar cells with Spiro-OMeTAD and MEH-PPV as the hole-transporting layer (HTL) by the one- and two-step methods for preparing perovskite with or without post-treatment by TiCl4 measured under 1 sun illumination.
Figure 5

(a) Current density–voltage (J–V) curves of perovskite solar cells with Spiro-OMeTAD and MEH-PPV as the HTMs by one- and two-step methods for preparing perovskite with or without post-treatment using TiCl4. PCE histograms from the one-step method with TiCl4 post-treatment for (b) Spiro-OMeTAD, (c) MEH-PPV and (d) PCE histograms from the two-step method with TiCl4 post-treatment for Spiro-OMeTAD with 10 cells.

Figure 6 shows the incident-photon-to-current-efficiency (IPCE) spectra of the perovskite solar cell. As can be observed, the generation of photocurrent began at 800 nm, which is in agreement with the bandgap of CH3NH3PbI3 and attained peak values of greater than 80% in the short-wavelength region of the visible spectra. These spectra indicate that the difference in JSC between one- and two-step methods for the preparation of perovskites with Spiro-OMeTAD is in full light absorption wavelength of perovskite and as compared to the Spiro-OMeTAD device, the MEH-PPV-based device exhibited a lower IPCE ranging from 300 to 500 nm, attributed to the light absorption of MEH-PPV (400–500 nm) in this region29. Although the cell performance of polymeric MEH-PPV was not better than that of Spiro-OMeTAD, their similar spectra still supports the view that MEH-PPV is an excellent HTM for perovskite solar cells. Notably, the conversion efficiency of the solar cells fabricated by the two-step method was greater than those by the one-step methods as reported previously, attributed to the submicrometer-sized CH3NH3PbI3 tetragonal crystals and the perfectly infiltrated PbI2 into the TiO2 mesoporous network2.

Figure 6

Incident-photon-to-current-efficiency (IPCE) spectra of perovskite solar cells with Spiro-OMeTAD and MEH-PPV as the HTMs by the one- or two-step method utilized for preparing perovskite layers.

Electrochemical impedance spectroscopy (EIS) was employed for quantifying the parameters of charge transport in solar cells, such as chemical capacitance, recombination resistance and charge conductivity. These parameters are imperative to aid in the explanation of the factors that determine the performance metrics of the HTMs in the corresponding solar cells and Table 2 summarizes the VOC, FF and JSC values. Figure 7 shows the (a) Nyquist and (b) Bode plots of the solar cells with different HTMs, which were recorded at VOC under 1 sun illumination. The frequency in EIS measurements ranged from 1 Hz to 1 MHz. The inset of Fig. 7a shows the fitting of the EIS spectra to an appropriate equivalent circuit model. Typically, Nyquist plots (Fig. 7a) were separated into two main regions or arcs at high and low frequencies; nevertheless, only one arc was observed under illumination. For convenience, a parallel charge-transfer resistance (RCT)–chemical capacitance (CCT) sub-circuit was applied, where recombination resistance (Rrec) and chemical capacitance (Crec) represent the charge recombination resistance and capacitance, respectively. Here, the absence of the recombination of electrons through a TiO2 network is attributed to the very thin TiO2 films and low electron transport resistance15. Hence, only one arc typically originates from the charge-transfer resistance at the interface between perovskite and HTMs in the devices. In accordance to a previous study on CH3NH3PbI3, a simplified circuit model (see inset of Fig. 7a) was utilized and the arc was assigned to the charge-transfer resistance in the devices15. As the devices predominantly differ with respect to the HTM, the arc is attributed to RCT and CCT at the interface between perovskite and HTMs. After photogenerated carriers were separated, holes transfer in the HTMs and electrons transfer in the TiO2 layer before arriving at both the electrodes. Hence, the charge-transfer resistance is one of the main factors limiting cell performance. From Table 2, as compared to the MEH-PPV based device, the Spiro-OMeTAD-based device exhibited a higher JSC under 1 sun illumination, indicative of better contact between Spiro-OMeTAD and perovskite as compared with that between MEH-PPV and perovskite. Hence, the charge-transfer resistance RCT simultaneously decreases because of better contact and easier charge transfer at the interface between perovskite and Spiro-OMeTAD. In addition, the electron lifetimes (τe) for the Spiro-OMeTAD and MEH-PPV-based devices were determined by Bode-phase plots. Figure 7b shows the Bode-phase plots of EIS spectra, which show the frequency peaks corresponding to charge transfer at different interfaces of Spiro-OMeTAD and MEH-PPV-based devices. From Fig. 7b and Table 2, the characteristic frequency peaks exhibited a shift toward lower frequencies for Spiro-OMeTAD-based devices as compared to MEH-PPV-based devices, implying a longer electron lifetime is observed for Spiro-OMeTAD-based devices. These observations imply that a better contact and charge transfer are observed between Spiro-OMeTAD and the perovskite layer.

Figure 7

Electrochemical impedance spectra (EIS), (a) Nyquist plot and (b) Bode plot for the perovskite solar cells with Spiro-OMeTAD and MEH-PPV as HTM at one-step or two-step method for perovskite layer preparation with TiCl4 post-treatment on mesoporous TiO2 layer. The equivalent circuit of this study is shown in the inset.


Spiro-OMeTAD was systematically investigated in comparison to the well-known hole-transporting polymer material MEH-PPV for solution-processed perovskite solar cells. The best performance for MEH-PPV was achieved by the one-step method for preparing the perovskite layer by post-treatment of the mesoporous TiO2 layer using TiCl4, with an η of 9.65% as well as hysteresis-free performance. The best performance for Spiro-OMeTAD was observed by the two-step method prepared using TiCl4-treated perovskite, exhibiting an η up to 13.38%. Our study demonstrated that MEH-PPV as a cost-effective, dopant-free HTM is a potential candidate for the development of perovskite solar cells in the future. Furthermore, as compared to Spiro-OMeTAD-based devices, which were typically affected by moisture, MEH-PPV-based devices without encapsulation exhibited higher stability against ambient moisture and we will further disclose it in other study.


Synthesis of methylammonium iodide

Methylammonium iodide (CH3NH3I) was prepared from 24 mL of methylamine solution (33% in ethanol) and diluted with 100 mL of absolute ethanol. A 10 mL aqueous solution of hydriodic acid (57 wt%) was added to this solution under constant stirring. After a reaction time of 1 h at room temperature, the solvents were removed by rotary evaporation. The obtained white solid was washed with dry diethyl ether and finally recrystallized from ethanol.

Device fabrication

FTO coated glass sheets (10 Ω □−1, Nippon Sheet Glass, 1.1 mm in thickness) were etched with zinc powder and HCl (2.0 M) to obtain the required electrode pattern. The sheets were then washed with 100 mL soap (2% Hellmanex® II in water), deionized water, acetone and 2-propanol and finally treated under UV ozone for 10 min to remove the last traces of organic residues. To make a dense TiO2 compact layer, the cleaned FTO glasses were coated with 0.15 M titanium diisopropoxide bis(acetylacetonate) (75% Aldrich) in 2-propanol (Wako) solution by the spin-coating method and heated at 125 °C for 5 min. After the coated film was cooled down to the room temperature, the same process was repeated twice with 0.3 M titanium diisopropoxide bis(acetylacetonate) solution in 2-propanol. The three times coated FTO glasses with TiO2 precursor solutions were heated at 550 °C for 15 min. The substrates were then coated with a commercially available screen-printable TiO2 paste (Solaronix, T/SP) mixed in 2:7 weight ratio with ethanol, prepared and sintered at 550 °C in air to achieve mesoporous TiO2 films. Afterward, the sintered TiO2 films were immersed in 0.02 M aqueous TiCl4 (Aldrich) solution at 70 °C for 60 min and heated at 550 °C for 30 min. For one-step method, the CH3NH3PbI3 perovskite precursor solution (CH3NH3I to PbI2 in 3:1 molar ratio, Sigma Aldrich 98%) was prepared to a concentration of 40 wt% in N-dimethylformamide (DMF) and spin coated onto the substrate under ambient atmosphere. The substrate was then transferred to a hotplate where it was heated in inert atmosphere to 100 °C for 90 min. This procedure allows for the formation of a perovskite layer in the mesoporous TiO2 film. For two-step method, the mesoporous TiO2 film were infiltrated with PbI2 by spin-coating a PbI2 solution in DMF (462 mg ml−1) that was kept at 70 °C for 30 min. After drying, the films were dipped into a solution of CH3NH3I in 2-propanol (10 mg ml−1) for 45 s and rinsed with 2-propanol for 10 s. After drying, the films were covered with a 400 nm layer of Spiro-OMeTAD (Merck). 96 mg of Spiro-OMeTAD was dissolved in 1 mL of chlorobenzene (CB) and mixed with 10 μL 4-tertbutylpyridine (tBP) and 40 μL of a 170 mg mL−1 bis(trifluoromethane)sulfonimide lithium salt (LiTFSI) solution in acetonitrile (ACN). This solution was spin coated at 3000 rpm for 45 s. In the second case, the hole-transport layer was obtained by a spin-coating in nitrogen atmosphere (glove box), poly(3-hexylthiophene-2,5-diyl) (P3HT, Rieke Metals, Inc., 15 mg mL−1, MW 50,000~70,000) solution in CB and 5-(2′-ethyl-hexyloxy)-p-phenylenevinylene (MEH-PPV, American Dye Source, Inc., MW 100,000~150,000, 5~15 mg mL−1) solution in CB, dichlorobenzene (DCB), or toluene with the following parameters: 600 rpm for 12 s and finally at 1500 rpm for 40 s; dried up at 90 °C for 10 min and 120 °C for 10 min. Before thermal depositing the gold electrodes, Spiro-OMeTAD was treated for oxidative doping in air overnight at room temperature and 30% relative humidity to enhance the conductivity; however, films of P3HT and MEH-PPV were employed as dopant-free without oxidation.

Solar cell characterization

Photocurrent density–voltage (J–V) characteristics were measured by a computer-controlled digital source meter (Keithley 2400) under 1 sun illumination. Irradiation of 100 mW cm−2 (1 sun) light was made with a Peccell Technologies, Inc. PEC-L11 solar simulator (AM 1.5G). All photovoltaic devices were masked with a thin black mask which was used to define the active area to be 0.1032 cm2. Bias voltage scanning was carried out at step voltage: 0.01 V; number of power line cycle (NPLC): 1 (20 ms); search delay: 0.05 s at scanning rate of 140 mV s−1. The incident photon to current efficiency (IPCE), or external quantum efficiency (EQE) action spectra of the device were measured by Keithley 2400 source meter in ambient air at room temperature on Peccell Technologies, Inc., PEC-S20 by scanning wavelength with 5 nm interval in conditions of a delay time of 5000 ms and under short-circuit condition (0 bias) of device. Absolute incident power density of monochromatic light in EQE measurement was monitored based on a standard Si photodetector.

Additional Information

How to cite this article: Chen, H.-W. et al. Efficiency Enhancement of Hybrid Perovskite Solar Cells with MEH-PPV Hole-Transporting Layers. Sci. Rep. 6, 34319; doi: 10.1038/srep34319 (2016).


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This study was partially sponsored by the Ministry of Science and Technology of Taiwan (MOST 102-2221-E-002-186-MY3) and the National Taiwan University. Some of the instruments utilized in this study were made available by the support of Academia Sinica of Taiwan and in part by the Japan Science and Technology Agency (JST) and the Advanced Low Carbon Technology R&D program (ALCA).

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H.-W.C. designed and performed the experiment. T.-Y.H. and T.-H.C. originated an idea in using the MEH-PPV material. C.-W.K. discussed with H.-W.C. about the details of the scientific results. Y.S. carried out scanning electron microscopic measurement. C.-W.C. implemented the idea and offered a glove box system and discussed with H.-W.C. M.I., T.M. and K.-C.H. supervised this study and revised the manuscript with lots of suggestions. H.-W.C. prepared the manuscript, to which all authors contributed many scientific suggestions.

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Chen, HW., Huang, TY., Chang, TH. et al. Efficiency Enhancement of Hybrid Perovskite Solar Cells with MEH-PPV Hole-Transporting Layers. Sci Rep 6, 34319 (2016).

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