Role of Molecular and Interchain Ordering in the Formation of a δ-Hole-Transporting Layer in Organic Solar Cells (original) (raw)

2019, ACS Applied Materials & Interfaces

Interface engineering, especially the realisation of ohmic contacts at the interface between organic semiconductors and metal contacts, is one of the essential preconditions to achieve high efficiency organic electronic devices. Here, the interface structure of polymer/fullerene blends are correlated with the charge extraction/injection properties of working organic solar cells. The model system-P3HT:PCBM-is fabricated using two different degrees of P3HT regioregularity to alter the blend interchain order and molecular packing, resulting in different device performance. Investigations by electroabsorption (EA) spectroscopy on these devices indicate a significant reduction (≈ 1 V) in the built-in potential with an increase in the P3HT regioregularity. This observation is also supported by a change in the WF of high regioregular polymer blends from photoelectron spectroscopy measurement. These results confirm the presence of a strong dipole layer acting as a δ-hole transporting layer at the polymer/MoO 3 /Ag electrode interface. Unipolar hole-only devices show an increase in the magnitude of the hole current in high regioregular P3HT devices, suggesting an increase in the hole injection/extraction efficiency inside device with a δ-hole transporting layer. Microscopically, near edge X-ray absorption fine structure (NEXAFS) spectroscopy was conducted to probe the surface microstructure in these blends finding a highly edge-on orientation of P3HT chains in blends made with high regioregular P3HT. This edge-on orientation of P3HT chains at the interface results in a layer of oriented alkyl side chains capping the surface which favors the formation of a dipole layer at the polymer/MoO 3 interface. The increase in the charge extraction efficiency due to the formation of a δ-hole transporting layer thus results in higher short circuit currents and fill factor values, eventually increasing the device efficiency in high regioregular P3HT devices despite a slight decrease in cell open circuit voltage. These findings emphasise the significance of work function control as a tool for improved device performance, and pave the way towards interfacial optimisation based on the modulation of fundamental polymer properties, such as polymer regioregularity.

Sign up to get access to over 50M papers

Sign up for access to the world's latest research

Dependence of mobility and charge injection on active layer thickness of bulk heterojunction organic solar cells: PCBM:P3HT

Optical and Quantum Electronics, 2020

The asymmetric behavior in the dark current of any solar cell is essential for decoupling recombination and charge extraction for efficient charge collection. Therefore current density dependence on applied voltage can be used to investigate the complex interplay between bulk charge transport, interface exchange effects and recombination mechanisms. In the present work, we investigate from dark current-density [J(V)] of bulk heterojunction solar cells, the dependence of mobility and charge injection mechanisms on different blend layer thicknesses. The active layer thickness has been established through varying the spin-coating speeds between 1000, 2000, 3000 and 4000 revolutions per minute (rpm) and confirmed by a dektak surface profilometer. The carrier mobility (μ) as a factor limiting the efficiency of organic solar cells was investigated from dark space charge limited current and trap free space charge limited current conduction mechanisms to distinguish between charge extraction and recombination. This approach allows the determination of the effects of threshold field through variation of the active layer thickness (ALT) on the potential barrier height (B) at the electrode contacts. Low values of charge carrier mobilities (10-6 cm 2 V −1 s −1) in the trap free space charge limited current conduction region have been correlated to the Langevin recombination constants. In the ohmic region, the highest dark carrier mobility corresponded to the 77.1 nm ALT. Further we observe a shift in the transition voltage at the inflection point of J-V curves with increasing film thickness in the forward bias.

Combined effects of carriers charge mobility and electrodes work function on the performances of polymer/fullerene P3HT:PCBM based organic photovoltaic solar cell

The European Physical Journal Applied Physics, 2018

This paper reports a study on the effect of different parameters such as charge carriers mobility, electrodes work function, energy gap, series as well as shunt resistances on the performances of an organic photovoltaic cell based on polymer/fullerene P3HT: PCBM. Thus, numerical simulations have been investigated on ITO/PEDOT:PSS/P3HT: PCBM/LiF/Al structure with Analysis of Microelectronic and Photonic Structures the simulation one dimension (AMPS-1D) and General-Purpose Photovoltaic Device Model (GPVDM) softwares. The results show that the optimum efficiency is obtained for electron and hole motility values of 10−4 cm2 V−1 s−1 and 2 × 10−4 cm2 V−1 s−1, respectively. Moreover, we reported that the ohmic contact for both anode and cathode electrodes of the investigated device remains very important to get the maximum efficiency. Furthermore, when the gap energy increases, the efficiency is considerably improved, and reach's a value of about 5.421%. In addition, in this present wo...

Effect of polydispersity on the bulk-heterojunction morphology of P3HT:PCBM solar cells

Journal of Polymer Science Part B: Polymer Physics

Bulk heterojunctions (BHJ) based on semiconducting electron-donor polymer and electronacceptor fullerene have been extensively investigated as potential photoactive layers for organic solar cells (OSCs). In the experimental studies, poly-(3-hexyl-thiophene) (P3HT) polymers are hardly monodisperse as the synthesis of highly monodisperse polymer mixture is a near impossible task to achieve. However, the majority of the computational efforts on poly-(3-hexylthiophene): phenyl-C61-butyric acid methyl ester (P3HT:PCBM) based OSCs, a monodisperse P3HT is usually considered. Here, results from coarse-grained molecular dynamics (CGMD) simulations of solvent evaporation and thermal annealing process of the BHJ are shared describing the effect of variability in molecular weight (a.k.a. polydispersity) on the morphology of the active layer. Results affirm that polydispersity is beneficial for charge separation as the interfacial area is observed to increase with higher dispersity. Calculations of percolation and orientation tensors, on the other hand, reveal that a certain polydispersity index (PDI) ranging between 1.05-1.10 should be maintained for optimal charge transport. Most importantly, these results point out that the consideration of polydispersity should be considered in computational studies of polymer based organic solar cells.

Organic Field-Effect Devices as Tool to Characterize the Bipolar Transport in Polymer-Fullerene Blends: The Case of P3HT-PCBM

Advanced Functional Materials, 2007

In organic bulk heterojunction solar cells (oBHJ) the blend morphology in combination with the charge transport properties of the individual components controls the extracted photocurrent. The organic field-effect transistor (OFET) has been proved as a powerful instrument to evaluate the unipolar carrier transport properties in a wide range of cases. In our work we extend the OFET concept to the evaluation of the bipolar transport properties in polymer-fullerenes blends and propose a method to improve the accuracy of the evaluation. The method is based on capacitance-voltage (C-V) measurements on MOS structures prepared on the same blends and delivers complementary information on the bulk heterojunction to the one obtained with FETs. The relevance for photovoltaic applications is investigated through the correlation between the current-voltage behavior of solar cells and the bipolar mobility for composites with varying polymer molecular weight and processed from different solvents. In particular the transport features of solar cells produced from o-Xylene (oX), a non chlorinated solvent more suitable to production requirements, have been compared to the one of devices cast from Chlorobenzene (CB) solution. For the P3HT-PCBM blend a consistent correlation between the mobility and the electrical fill factor and power performance was found. A significant asymmetry in the bipolar carrier mobility, together with low electron mobility dependent on the M w value, affects the performances of thick o-Xylene cast devices. In the case of devices processed from Chlorobenzene the slower carrier has higher mobility and the small electrical losses detected are eventually more related to the formation of space-charge and eventually to surface recombination. This results in an efficient charge collection that is almost thickness independent. We report a dependence of the slow-carrier type (electrons or holes) and their mobility on the specific combination of molecular weight and solvent. The mobility data and the solar cell performance coherently fit to the prediction of a device model only based on the drift of carriers under the built-in electric field originated in the donor-acceptor oBHJ.

Loading...

Loading Preview

Sorry, preview is currently unavailable. You can download the paper by clicking the button above.