C61-butyric Acid Methyl Ester Research Articles

Improving photovoltaic characteristics of CdS-based hybrid solar cells through Mn incorporation

CdS thin films, both with and without Mn-doping, were grown via chemical bath deposition on indium tin oxide-coated glass substrates for application in hybrid solar cells. X-ray diffraction analysis revealed that Mn doping led to a deterioration in the crystal quality of CdS samples, evidenced by increased microstrain and dislocation density. Mn atoms were interstitially incorporated into the CdS structure, resulting in an expansion of the unit cell volume. Morphological analysis indicated a decrease in grain size from 390 nm to 140 nm for 0 % and 2 % Mn-doped CdS samples, respectively, while maintaining the spherical shape of the CdS thin films. Mn doping also increased the transmittance of CdS thin films, with the highest transparency of 95 % at 580 nm achieved for the 2 % Mn-doped CdS sample. In comparison to undoped CdS (2.38 eV), the band gap of CdS samples initially decreased to 1.84 eV for 1 % Mn doping but significantly increased to 3.03 eV for 2 % Mn-doped CdS. Photoluminescence (PL) data indicated that 2 % Mn-doped CdS thin films exhibited the lowest peak intensity, suggesting that a high concentration of Mn atoms caused non-radiative charge recombination. Additionally, efficient exciton dissociation was observed between CdS:Mn and P3HT:PCBM (poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM)) layers in the 2 % Mn-doped CdS-based device, as per the PL results. Photovoltaic measurements demonstrated that compared to undoped CdS, 2 % Mn doping increased the power conversion efficiency of the CdS-based device from 0.070 % to 0.202 %, indicating an almost threefold increase in hybrid solar cell efficiency. This improvement is likely attributed to the development of a better interface between the CdS:Mn and P3HT:PCBM layers.

Interface passivation using diketopyrrolopyrrole‐oligothiophene copolymer to improve the performance of perovskite solar cells

AbstractThe unprecedented increase in power conversion efficiency (PCE) of low‐cost organo‐inorganic halide perovskite solar cells (OIHPSCs) toward its Shockley‐Queisser limit intriguingly has prompted researchers to investigate the disadvantages of these devices. The issue of operational stability is the main hurdle challenging the way forward for commercialization. To address this, various engineering processes like composition, additives, anti‐solvents, bulk and interface passivation, and deposition techniques have been widely applied to manage both extrinsic and intrinsic factors that induce degradation of the OIHPSCs. In this work, we employed interface passivation, which is an efficient approach to reduce nonradiative recombination. An ultrathin layer of electron donor diketopyrrolopyrrole‐oligothiophene copolymer (DPP860) was applied as an interface passivator between the photoactive layer and [6,6]‐phenyl C61 butyric acid methyl ester (PCBM). The role of the interface passivation on optoelectronic properties of the OIHPSCs was assessed using current density versus voltage (J‐V) characteristics, photoluminescence spectroscopy and time‐resolved photoluminescence spectroscopy. The findings show devices treated with DPP860 exhibit enhanced current density (Jsc) and fill factor, attributing for suppressed nonradiative recombination. Moreover, it shows relative improvement in the stability of the device. The results of this finding reveal that using oligothiophene copolymer can enhance the photovoltaic performance and the stability of inverted OIHPSCs in the ambient environment.

Influence of the electron transport layer coating technique on sputter damage and its curing in inverted semi-transparent perovskite solar cells without protective buffer layer

In semi-transparent perovskite solar cells (PSCs) comprising a sputtered top electrode, the minimisation of detrimental sputter damage and/or its curing by post-processing treatment is essential to reach high efficiencies. In this work, we investigate the influence of sputter damage and post-deposition annealing steps for different electron transport layers (ETLs) in PSCs without the need of a protective buffer layer such as tin oxide deposited by atomic layer deposition. We compare solution-processed 6,6-Phenyl C61 butyric acid methyl ester (PCBM) to thermally evaporated C60, each in combination with a bathocuproine (BCP) layer deposited by spin coating or thermal evaporation including a thickness variation. In general, we find that C60 is more resilient against sputter damage and thus C60-based cells show higher as-grown power conversion efficiencies (PCEs). Post-deposition annealing of the complete cell stack increases the PCE further to values > 16 % on 0.5 cm2 active area. However, we observe that the remaining solvent in the spin-coated PCBM layer is highly beneficial for the curing of the sputter damage during post-deposition annealing and we achieve even higher PCEs for cells incorporating solution-processed PCBM with up to > 18 % on 0.5 cm2. We show an alternative way to reach high efficiency semi-transparent perovskite solar cells without using thermally evaporated C60 and/or a buffer layer like tin oxide deposited by atomic layer deposition (ALD).

Fluorinated organic ammonium salt passivation for high-efficiency and stable inverted CsPbI2Br perovskite solar cells.

All-inorganic CsPbI2Br inverted perovskite solar cells (PSCs) have drawn increasing attention because of their outstanding thermal stability and compatible process with tandem cells. However, relatively low open circuit voltage (Voc) has lagged their progress far behind theoretical limits. Herein, we introduce phenylmethylammonium iodide and 4-trifluoromethyl phenylmethylammonium iodide (CFPMAI) on the surface of a CsPbI2Br perovskite film and investigate their passivation effects. It is found that CFPMAI with a -CF3 substituent significantly decreases the trap density of the perovskite film by forming interactions with the under-coordinated Pb2+ ions and effectively suppresses the non-radiative recombination in the resulting PSC. In addition, CFPMAI surface passivation facilitates the optimization of energy-level alignment at the CsPbI2Br perovskite/[6,6]-phenyl C61 butyric acid methyl ester interface, resulting in improved charge extraction from the perovskite to the charge transport layer. Consequently, the optimized inverted CsPbI2Br device exhibits a markedly improved champion efficiency of 14.43% with a Voc of 1.12V, a Jsc of 16.31 mA/cm2, and a fill factor of 79.02%, compared to the 10.92% (Voc of 0.95V) efficiency of the control device. This study confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement.

Effective surface passivation for stable and high-performance inverted CsPbI2Br perovskite solar cells with efficiency over 15%

Inverted CsPbI2Br perovskite solar cells (PSCs) still suffer from substantially non-radiative recombination losses at the perovskite interface, which limits the future advancement of CsPbI2Br perovskite-based single- and multi-junction photovoltaic cells. Interfacial defect passivation of perovskite films is an effective approach for enhancing the performance of PSCs. In this study, we introduce thiophene halide salts with different side groups on the surface of CsPbI2Br films to passivate the inorganic perovskite film and investigate their passivation effects. Our studies show that the 2-thiophenemethylammonium iodide (TM) passivator with –CH2NH3I side group effectively mitigates the trap density of the perovskite film by forming coordination bonding with Pb2+ ions, thus significantly inhibiting the non-radiative recombination in the resulting PSC. In addition, after the TM treatment, the better energy-level alignment between the CsPbI2Br/[6,6]-Phenyl C61 butyric acid methyl ester (PCBM) interface is achieved, thus enhancing the charge extraction from perovskite to the charge transport layer. The resulting inverted CsPbI2Br device demonstrates a significantly enhanced champion efficiency of 15.07% with a Voc of 1.16 V, Jsc of 16.42 mA/cm2, and FF of 79.11%, compared to the 11.19% efficiency of the control device, and maintains >97% of the initial efficiency after being stored for over 1700 h in N2 atmosphere. This work confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement.

Toward Low-Voltage and High-Sensitivity Direct X-ray Detectors Based on Thick Bulk Heterojunction Organic Device.

Organic semiconducting materials are promising for the fabrication of flexible ionizing radiation detectors for imaging because of their tissue equivalence, simple large-scale processing, and mass production. However, it is challenging to achieve high-sensitivity detection for organic direct detectors prepared by low-cost solution processing because of the compromise between thickness and carrier transport. In this study, high-performance organic direct X-ray detectors were fabricated by building a micrometer-thick bulk heterojunction (BHJ) using poly(3-hexylthiophene-2,5-diyl) (P3HT):(6,6)-phenyl c71 butyric acid methyl ester. A 5 μm BHJ film was fabricated by drop-casting and enhanced crystallization of P3HT using binary solvents and high-boiling-point additives to improve the charge carrier mobility. Furthermore, this organic direct X-ray detector has a sensitivity of >654.26 μC Gyair s-1 and a self-powered response. Because of the architecture of the thick active layer and the energy cascade in this diode detector, it has a very low dark current of 46.26 pA at -2 V. A fast and efficient approach was developed for fabricating thick, highly mobile organic BHJ films for high-performance direct X-ray detectors. It has great potential for application in a new generation of flexible and portable large-area flat-panel detectors.

Insulating 6,6-Phenyl-C61-butyric Acid Methyl Ester on Transition-Metal Dichalcogenides: Impact of the Hybrid Materials on the Optical and Electrical Properties.

In this study we develop a strategy to insulate 6,6 -Phenyl C61 butyric acid methyl ester (PCBM) on the basal plane of transition metal dichalcogenides (TMDs). Concretely single layers of MoS2, MoSe2, MoTe2, WS2, WSe2 and WTe2 and ultrathin MoO2 and WO2 were grown via chemical vapor deposition (CVD). Then, the thiol group of a PCBM modified with cysteine reacts with the chalcogen vacancies on the basal plane of TMDs, yielding PCBM-MoS2, PCBM-MoSe2, PCBM-WS2, PCBM-WSe2, PCBM-WTe2, PCBM-MoO2 and PCBM-WO2. Afterwards, all the hybrid materials were characterized using several techniques, including XPS, Raman spectroscopy, TEM, AFM, and cyclic voltammetry. Furthermore, PCBM causes a unique optical and electrical impact in every TMDs. For MoS2 devices, the conductivity and photoluminescence (PL) emission achieve a remarkable enhancement of 1700 % and 200 % in PCBM-MoS2 hybrids. Similarly, PCBM-MoTe2 hybrids exhibit a 2-fold enhancement in PL emission at 1.1 eV. On the other hand, PCBM-MoSe2, PCBM-WSe2 and PCBM-WS2 hybrids exhibited a new interlayer exciton at 1.29-1.44, 1.7 and 1.37-154 eV along with an enhancement of the photo-response by 2400, 3200 and 600 %, respectively. Additionally, PCBM-WTe2 and PCBM-WO2 showed a modest photo-response, in sharp contrast with pristine WTe2 or WO2 which archive pure metallic character.

Effect of Anode Interfacial Modification by Self-Assembled Monolayers on the Organic Solar Cell Performance.

A series of self-assembled monolayer (SAM)-based benzoic acid derivatives such as 4-[5'-phenyl-2,2'-bitien-5-yl] benzoic acid (ZE-Ph), 4-[5'-(4-fluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-1F), and 4-[5'-(3,5-difluorophenyl)-2,2'-bitien-5-yl]benzoic acid (ZE-2F) were synthesized to use an interlayer between an ITO electrode and a MoO3 thin film layer in an organic solar cell (OSC) having poly-3 hexylthiophene (P3HT): [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) blend. The work function and surface wetting properties of the ITO were tuned by SAM molecules. The power conversion efficiency of fabricated OSC devices was improved compared to that of the control device from 1.93 to 2.20% and 2.22% with ZE-Ph and ZE-1F-modified ITO electrodes, respectively. The short-circuit current density (Jsc) was increased from 6.16 to 7.10 mA/cm2 and 6.94 mA/cm2 with control, ZE-Ph, and ZE-1F-modified solar cells, respectively. The increase in short-circuit current density (Jsc) shows that the hole-transporting properties between ITO and MoO3 were improved by the use of ZE-Ph and ZE-1F compared with that of the ITO/MoO3 electrode configuration. The open-circuit voltage (Voc) of the SAM-modified ITO-based devices was also improved compared with the Voc of unmodified ITO-based devices. These results show that using a monolayer as an interlayer in OSCs is an important strategy to improve the performance of OSCs. All the device parameters were characterized by Kelvin probe force microscopy, cyclic voltammetry, contact angle, and I-V measurements.

Enhanced Efficiency and Stability of Inverted CsPbI2Br Perovskite Solar Cells via Fluorinated Organic Ammonium Salt Surface Passivation.

All-inorganic perovskite solar cells (PSCs) have recently received increasing attention due to their outstanding thermal stability. However, the performance of these devices, especially for the devices with a p-i-n structure, is still inferior to that of the typical organic-inorganic counterparts. In this study, we introduce phenylammonium iodides with different side groups on the surface of the CsPbI2Br perovskite film and investigate their passivation effects. Our studies indicate that the 4-trifluoromethyl phenylammonium iodide (CFPA) molecule with the -CF3 side group effectively decreases the trap density of the perovskite film by forming interactions with the undercoordinated Pb2+ ions and significantly inhibits the nonradiative recombination in the derived PSC, leading to an enhanced open-circuit voltage (Voc) from 0.96 to 1.10 V after passivation. Also, the CFPA post-treatment enables better energy-level alignment between the conduction band minimum of CsPbI2Br perovskite and [6,6]-phenyl C61 butyric acid methyl ester, thereby enhancing the charge extraction from the perovskite to the charge transport layer. These combined benefits result in a significant enhancement of the power conversion efficiency from 11.22 to 14.37% for inverted CsPbI2Br PSCs. The device without encapsulation exhibits a degradation of only ≈4% after 1992 h in a N2 glovebox.

A Three-Dimensional Non-Fullerene Acceptor with Contorted Hexabenzocoronene and Perylenediimide for Organic Solar Cells.

Although fullerene derivatives such as [6,6]-phenyl-C61/C71-butyric acid methyl ester (PC61BM/PC71BM) have dominated the the photoactive acceptor materials in bulk heterojunction organic solar cells (OSCs) for decades, they have several drawbacks such as weak absorption, limited structural tunability, prone to aggregation, and high costs of production. Constructing non-fullerene small molecules with three-dimensional (3D) molecular geometry is one of the strategies to replace fullerenes in OSCs. In this study, a 3D molecule, contorted hexa-cata-hexabenzocoronene tetra perylenediimide (HBC-4-PDI), was designed and synthesized. HBC-4-PDI shows a wide and strong light absorption in the whole UV-vis region as well as suitable energy levels as an acceptor for OSCs. More importantly, the 3D construction effectively reduced the self-aggregation of c-HBC, leading to an appropriate scale phase separation of the blend film morphology in OSCs. A preliminary power conversion efficiency of 2.70 % with a champion open-circuit voltage of 1.06 V was obtained in OSCs with HBC-4-PDI as the acceptor, which was the highest among the previously reported OSCs based on c-HBC derivatives. The results indicated that HBC-4-PDI may serve as a good non-fullerene acceptor for OSCs.

Equal proportion of donor/acceptor active layer for reduced dark current in visible organic photodiode

The present study investigates a visible organic photodiode with low dark current of 0.002 mA/cm2. The active layer is a bulk heterojunction (BHJ) binary blended film composed of Poly[N-9′-heptadecanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)] (PCDTBT) as a donor material along with (6,6)-Phenyl C71 butyric acid methyl ester (PC71BM) as an acceptor material. The device was fabricated using a facile spin coating technique with the structure of ITO/PEDOT:PSS/PCDTBT:PC71BM/Al. The composition of PCDTBT and PC71BM has significantly improved the absorption of the UV–visible spectrum, especially between 300 and 650 nm. The optimized device of the blended film (1:1 blend ratio) showed a good photoresponsivity of 114 mA/W, with a fast response-recovery time of 733 ms and 597 ms, respectively. It is found that the specific detectivity obtained is 1.79×109 Jones and external quantum efficiency (EQE) is 29.13 %. The results manifested the optimized device can be employed in the fabrication of a cost-effective and highly sensitive visible organic photodiode.

The novel n-channel liquid crystal organic field effect transistor (LC-n-OFET): A promising technology for low-power electronics

In this study, a novel n-channel liquid crystal organic field effect transistor (LC-n-OFET) was fabricated using a mixture of E7 nematic liquid crystal (NLC) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) in an OFET cell. The LC-n-OFET performance was investigated regarding dielectric properties, UV illumination sensitivity, and channel length dependence. Output and transfer current-voltage (I–V) characteristics were measured to evaluate the electrical properties in dark and under UV illumination for varying channel lengths. Additionally, the dielectric characteristics of the LC-n-OFET were determined along with the capacitance-frequency response (Ci-f), threshold voltage (VTh), field-effect mobility (μFET), and on/off current ratio (Ion/off) as a function of UV illumination intensity and channel length changes. Electrical measurements showed the Ion/off current ratio is inversely proportional to channel length but directly proportional to UV intensity. Meanwhile, the threshold voltage (VTh) and mobility (μFET) increased with longer channel length and higher light intensity. Overall, the novel LC-n-OFET exhibited promising performance with low VTh, high μFET, and large Ion/off.

Scalable Solution-Processed Hybrid Electron Transport Layers for Efficient All-Perovskite Tandem Solar Modules.

All-perovskite tandem solar cells offer the potential to surpass the Shockley-Queisser (SQ) limit efficiency of single-junction solar cells while maintaining the advantages of low-cost and high-productivity solution processing. However, scalable solution processing of electron transport layer (ETL) in p-i-n structured perovskite solar subcells remains challenging due to the rough perovskite film surface and energy level mismatch between ETL and perovskites. Here, scalable solution processing of hybrid fullerenes (HF) with blade-coating on both wide-bandgap (≈1.80 eV) and narrow-bandgap (≈1.25 eV) perovskite films in all-perovskite tandem solar modules is developed. The HF, comprising a mixture of fullerene (C60 ), phenyl C61 butyric acid methyl ester, and indene-C60 bisadduct, exhibits improved conductivity, superior energy level alignment with both wide- and narrow-bandgap perovskites, and reduced interfacial nonradiative recombination when compared to the conventional thermal-evaporated C60 . With scalable solution-processed HF as the ETLs, the all-perovskite tandem solar modules achieve a champion power conversion efficiency of 23.3% (aperture area = 20.25 cm2 ). This study paves the way to all-solution processing of low-cost and high-efficiency all-perovskite tandem solar modules in the future.

Tissue Equivalent Curved Organic X-ray Detectors Utilizing High Atomic Number Polythiophene Analogues.

Organic semiconductors are a promising material candidate for X-ray detection. However, the low atomic number (Z) of organic semiconductors leads to poor X-ray absorption thus restricting their performance. Herein, the authors propose a new strategy for achieving high-sensitivity performance for X-ray detectors based on organic semiconductors modified with high -Z heteroatoms. X-ray detectors are fabricated with p-type organic semiconductors containing selenium heteroatoms (poly(3-hexyl)selenophene (P3HSe)) in blends with an n-type fullerene derivative ([6,6]-Phenyl C71 butyric acid methyl ester (PC70 BM). When characterized under 70, 100, 150, and 220kVp X-ray radiation, these heteroatom-containing detectors displayed a superior performance in terms of sensitivity up to 600 ± 11nCGy-1 cm-2 with respect to the bismuth oxide (Bi2 O3 ) nanoparticle (NP) sensitized organic detectors. Despite the lower Z of selenium compared to the NPs typically used, the authors identify a more efficient generation of electron-hole pairs, better charge transfer, and charge transport characteristics in heteroatom-incorporated detectors that result in this breakthrough detector performance. The authors also demonstrate flexible X-ray detectors that can be curved to a radius as low as 2mm with low deviation in X-ray response under 100 repeated bending cycles while maintaining an industry-standard ultra-low dark current of 0.03 ± 0.01pAmm-2 .

Efficient and Stable Air-Processed Ternary Organic Solar Cells Incorporating Gallium-Porphyrin as an Electron Cascade Material.

Two gallium porphyrins, a tetraphenyl GaCl porphyrin, termed as (TPP)GaCl, and an octaethylporphyrin GaCl porphyrin, termed as (OEP)GaCl, were synthesized to use as an electron cascade in ternary organic bulk heterojunction films. A perfect matching of both gallium porphyrins' energy levels with that of poly(3-hexylthiophene-2,5-diyl) (P3HT) or poly[N-9'-heptadecanyl-2,7-carbazole-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT) polymer donor and the 6,6-phenyl C71 butyric acid methyl ester (PCBM) fullerene acceptor, forming an efficient cascade system that could facilitate electron transfer between donor and acceptor, was demonstrated. Therefore, ternary organic solar cells (OSCs) using the two porphyrins in various concentrations were fabricated where a performance enhancement was obtained. In particular, (TPP)GaCl-based ternary OSCs of low concentration (1:0.05 vv%) exhibited a ~17% increase in the power conversion efficiency (PCE) compared with the binary device due to improved exciton dissociation, electron transport and reduced recombination. On the other hand, ternary OSCs with a high concentration of (TPP)GaCl (1:0.1 vv%) and (OEP)GaCl (1:0.05 and 1:0.1 vv%) showed the poorest efficiencies due to very rough nanomorphology and suppressed crystallinity of ternary films when the GaCl porphyrin was introduced to the blend, as revealed from X-ray diffraction (XRD) and atomic force microscopy (AFM). The best performing devices also exhibited improved photostability when exposed to sunlight illumination for a period of 8 h than the binary OSCs, attributed to the suppressed photodegradation of the ternary (TPP)GaCl 1:0.05-based photoactive film.

Hybrid photonic device based on Graphene Oxide (GO) doped P3HT-PCBM/p-Silicon for photonic applications

Graphene oxide (GO) doped poly(3-hexylthiophene):[6,6]-phenyl C61 butyric acid methyl ester (P3HT:PCBM) interlayered Al/p-Si Schottky barrier diodes (SBDs) were manufactured by spin coating technique and investigated for the effects of GO concentration on electrical and photodiode parameters. The current–voltage (I-V), measurements for the different mass ratios of GO:P3HT:PCBM (0:1:1(S1), 0.5:1:1(S2) and 2:1:1(S3)) used diodes allowed the determination of key electrical parameters, including ideality factor (n), barrier height (Φ B ), series resistance (R s ), shunt resistance (R sh ), interface states density (N ss ) and optical sensing behaviors in dark and different illumination levels (10, 30, 60, 80 and 100 mW cm−2). The rectification ratio (RR) was found to be in the order of 104. The trends obtained for the n, Φ B , R s /R sh and N ss show that these are influenced by the contribution of the GO. Observed increasing behavior of reverse current with increasing illumination shows that this SBDs can be use as photo-diodes/sensors/detectors. On the other hand, it was observed that the linear dynamic range (LDR), which is important parameter for image sensors, increased (6.86, 16.95 and 26.98 for S1, S2 and S3, respectively) with increasing GO contribution. In addition, to investigate and compare in more detail, capacitance–voltage (C-V) and conductance-voltage (G-V) measurements used for the determination of diffusion potential (V D ), concentration of dopant acceptor atoms (N A ), Fermi energy level (E F ), depletion layer width (W D ) for low frequency (1 kHz) and high frequency (1 MHz). The measured capacitance values showed a high value at the low frequency in comparison with the high frequency. This behavior explained on the basis of N ss . The findings suggest that the prepared diodes has the potential to serve as a photo-diodes/sensors/detectors for optical sensing applications.

Supramolecular interaction of PCBM with porphyrins in solution: Photophysical insights

This work reports the self-assembly between [6,6]-phenyl C71 butyric acid methyl ester (PCBM) and 2,3,7,8,12,13,17,18-octaethyl-21H,23H porphyrin (1)(and/2,3,7,8,12,13,17,18-octaethyl-21H,23H porphyrin Zn(II) (2) in toluene. Ground state intermolecular interaction is evidenced from absorption spectrophotometric measurements. New absorption bands are observed in the visible region which may be identified due to charge transfer (CT). Several important physicochemical factors are enumerated for PCBM-1 and PCBM-2 systems. Fluorescence investigations elicit complex formation of PCBM with porphyrins (with both 1 and 2) and reveal considerable magnitude of binding constant (K) for PCBM-2 system, i.e., KPCBM-2 = 80,435 dm3⋅mol−1 compared to PCBM-1 system, i.e., KPCM-1 = 12,600 dm3·mol-1 as well as highly ratio of selectivity in binding (KPCBM-2/KPCBM-1 ∼ 6.4). Time resolved fluorescence experiments reveal that photoexcited decay from the excited singlet state of porphyrins (i.e., 1* and 2*) by PCBM is statically controlled compared to dynamic path. Magnitude of solvent reorganization energy indicates possibility of faster charge recombination in case of PCBM-2 system. Both 1H and 13C NMR measurements provide substantial support behind complexation of PCBM with porphyrins (both 1 and 2) in solution. Ab initio calculations in vacuo support the trend in K for PCBM-1 and PCBM-2 systems and establish the proper orientation of PCBM towards 1 (and/ 2) during complexation. Transient absorption measurements establish two different mode of energy transfer pathway from porphyrin to PCBM in toluene.

Enhancing efficiency and decelerating degradation in bulk heterojunction solar cells with N,N-Dimethylformamide cosolvent for poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)

Focused on the improvement of hole transport layer of organic solar cells based on poly(3-hexylthiophene) (P3HT)/6,6-phenil C61-butyric acid methyl ester (PCBM) blend, we studied the possibility of extending the lifetime of these devices. Thus, influence of N,N-dimethylformamide (DMF) added to poly(3,4-ethylenedioxythiofene):poly(styrenesulfonate) (PEDOT:PSS) hole transport layer was analyzed. We report that DMF causes an increase in the power conversion efficiency (PCE) of organic solar cells. A likely reason for this improvement might be a reduced intermolecular distance between the poly(3,4-ethylenedioxythiofene): (PEDOT) and poly(styrenesulfonate) (PSS) chains. The optimal volume of DMF in PEDOT:PSS was studied: two parts of DMF to one part of PEDOT:PSS increases PCE by 47%. Furthermore, PEDOT:PSS layer with DMF generated a reduction in the degradation of PCE, extending the lifetime of bulk heterojunction solar cells.

Silver Nanoparticle-PEDOT:PSS Composites as Water-Processable Anodes: Correlation between the Synthetic Parameters and the Optical/Morphological Properties.

The morphological, spectroscopic and rheological properties of silver nanoparticles (AgNPs) synthesized in situ within commercial PEDOT:PSS formulations, labeled PP@NPs, were systematically investigated by varying different synthetic parameters (NaBH4/AgNO3 molar ratio, PEDOT:PSS formulation and silver and PEDOT:PSS concentration in the reaction medium), revealing that only the reagent ratio affected the properties of the resulting nanoparticles. Combining the results obtained from the field-emission scanning electron microscopy analysis and UV-Vis characterization, it could be assumed that PP@NPs' stabilization occurs by means of PSS chains, preferably outside of the PEDOT:PSS domains with low silver content. Conversely, with high silver content, the particles also formed in PEDOT-rich domains with the consequent perturbation of the polaron absorption features of the conjugated polymer. Atomic force microscopy was used to characterize the films deposited on glass from the particle-containing PEDOT:PSS suspensions. The film with an optimized morphology, obtained from the suspension sample characterized by the lowest silver and NaBH4 content, was used to fabricate a very initial prototype of a water-processable anode in a solar cell prepared with an active layer constituted by the benchmark blend poly(3-hexylthiophene) and [6,6]-Phenyl C61 butyric acid methyl ester (PC60BM) and a low-temperature, not-evaporated cathode (Field's metal).

The impact of Ag/Co nanocomposite on organic charge transport medium for improved photocurrent in polymer solar cell

AbstractTuning charge transport properties using silver‐cobalt bimetallic nanoparticles is investigated to enhance the photo‐current collection in polymer solar cells. The silver‐cobalt nanoparticles were not only augmenting the charge transport processes but also expected to trap light by way of reflection. The polymers blend consisting of poly‐(3‐hexylthiophene) (P3HT):[6,6]‐phenyl C61 butyric acid methyl ester (PC61BM) is used in the fabrication of polymer solar cells. The experimental results indicated that the solar cells' performance depended on the concentration of Ag/Co in the hole transport layer (HTL). Nevertheless, the high‐power conversion efficiency value of up to 4.21% was observed, at the concentration of 0.1% by weight, which is much higher than pristine solar cells due to improved measured photocurrents from the devices. This is a significant improvement in PCE by 66.4% compared to the undoped transport medium. Ag/Co nanocomposite is found to be more stable under ambient laboratory conditions.