Kung-Shih Chen

Development of New Conjugated Polymers with Donor−π-Bridge−Acceptor Side Chains for High Performance Solar Cells

Two new conjugated polymers have been designed and synthesized for polymer solar cells. Both of them exhibit excellent photovoltaic properties with a power conversion efficiency as high as 4.74%. Different from the traditional linear donor-acceptor (D-A) type conjugated polymers, these newly designed polymers have a two-dimensional conjugated structure with their tunable acceptors located at the end of D-A side chains and connected with the donors on the main chain through an efficient pi-bridge. This approach provides great flexibility in fine-tuning the absorption spectra and energy levels of the resultant polymers for achieving high device performance.

Surface Doping of Conjugated Polymers by Graphene Oxide and Its Application for Organic Electronic Devices

Conjugated polymers are a novel class of solution-processable semiconducting materials with intriguing optoelectronic properties. [ 1 ] They have received great attention as active components in organic electronic devices such as organic photovoltaic cells (OPVs), organic light-emitting diodes (OLEDs), and organic fi eld-effect transistors (OFETs) due to their light weight, facile tuning of electronic properties through molecular engineering, and ease of processing. The performance and lifetime of conjugated polymer-based electronic devices are critically dependent on the bulk properties of the active materials and the interfacial properties of electrode/polymer contacts. [ 2–4 ] In these devices, the electrode(s) either inject charge into or extract charges from the organic semiconductor layer(s). Mismatch of the work functions between metal or metal oxide electrodes and molecular orbital energy levels of organic semiconductors can lead to high contact resistance, which decreases the charge injection and extraction effi ciency. Therefore, it is essential to minimize contact resistance at the electrode/organic semiconductor interface. To improve charge injection/extraction across the electrode/ organic semiconductor interface, several strategies have been developed. One is to tune the interfacial dipole across the electrode/semiconductor interface to reduce the injection/collection energy barrier. This can be achieved by modifying the electrode surface with self-assembled dipolar molecules to tune the energy level alignment at the semiconductor/electrode interface. [ 5–7 ] Alternatively, the introduction of a thin layer of polymer surfactant that contains polar side chains between the conjugate polymer/electrode interface can also be used to improve the interfacial properties. The polar side chains can provide not

Increased open circuit voltage in fluorinated benzothiadiazole-based alternating conjugated polymers

Small band-gap conjugated polymers based on monofluoro- and difluoro-substituted benzothiadiazole were developed. Highly efficient polymer solar cells (PCE as high as 5.40%) could be achieved for devices made from these polymers.

Semi-transparent polymer solar cells with 6% PCE, 25% average visible transmittance and a color rendering index close to 100 for power generating window applications

Inverted semi-transparent organic photovoltaic (OPV) cells with very high device performance, tunable transparency, and extraordinary transparency color perception and rendering properties have been demonstrated for power-generating window applications for buildings and automotives.

Conjugated polymers based on C, Si and N-bridged dithiophene and thienopyrroledione units: synthesis, field-effect transistors and bulk heterojunction polymer solar cells

A series of low band-gap conjugated polymers (PDTC, PDTSi and PDTP) containing electron-rich C-, Si-, and N-bridged bithiophene and electron-deficient thienopyrroledione units were synthesized viaStille coupling polymerization. All these polymers possess a low-lying energy level for the highest occupied molecular orbital (HOMO) (as low as −5.44 eV). As a result, photovoltaic devices derived from these polymers show high open circuit voltage (Voc as high as 0.91 V). These rigid polymers also possess respectable hole mobilities of 1.50 × 10−3, 6.0 × 10−4, and 3.9 × 10−4 cm2 V−1s−1 for PDTC, PDTSi, and PDTP, respectively. The combined high Voc and good hole mobility enable bulk hetero-junction photovoltaic cells to be fabricated with relatively high power conversion efficiency (PCE as high as 3.74% for the PDTC-based device).

Microcavity‐Enhanced Light‐Trapping for Highly Efficient Organic Parallel Tandem Solar Cells

A high-performance parallel tandem solar cell employing ultra-thin Ag as the intermediate anode is demonstrated, which comprises a semitransparent front sub-cell and a microcavity assisted back sub-cell. In addition to the extended optical field as a result of the tandem architecture, the prominent microcavity resonance formed in the back sub-cell enables such a parallel tandem configuration to possess high light utilization efficiency (the peak EQE value is over 80%) and a high photovoltaic performance of 9.2%. This study establishes an effective architecture that can be generally applicable to all organic materials for improving their performance.

Strong photocurrent enhancements in highly efficient flexible organic solar cells by adopting a microcavity configuration.

Organic solar cells often show inefficient light harvesting due to a short absorption path length limited by the low charge mobility of organic semiconductors. We demonstrate a flexible organic solar cell in a microcavity configuration using a TeO2/Ag semitransparent electrode to confine the optical field within the device with significant performance improvements and reaching a power conversion efficiency of 8.56%.

n-Doping of thermally polymerizable fullerenes as an electron transporting layer for inverted polymer solar cells

A novel [6,6]-phenyl-C61-butyric acid methyl styryl ester (PCBM-S) was synthesized and employed as an electron transporting interfacial layer for bulk heterojunction polymer solar cells with an inverted device configuration. After the deposition of PCBM-S film from solution, the styryl groups of PCBM-S were polymerized by post-thermal treatment to form a robust film which is resistive to common organic solvents. This allows the solution processing of upper bulk heterojunction film without eroding the PCBM-S layer. Additionally, the PCBM-S was n-doped with decamethylcobaltocene (DMC) to increase the conductivity of the film, which resulted in a significantly improved power conversion efficiency from 1.24% to 2.33%. The improved device performance is due to the decrease of series resistance and improved electron extraction property of the n-doped PCBM-S film.

Polymer Triplet Energy Levels Need Not Limit Photocurrent Collection in Organic Solar Cells

We study charge recombination via triplet excited states in donor/acceptor organic solar cells and find that, contrary to intuition, high internal quantum efficiency (IQE) can be obtained in polymer/fullerene blend devices even when the polymer triplet state is significantly lower in energy than the intermolecular charge transfer (CT) state. Our model donor system comprises the copolymer PIDT-PhanQ: poly(indacenodithiophene-co-phenanthro[9,10-b]quinoxaline), which when blended with phenyl-C(71)-butyric acid methyl ester (PC(71)BM) is capable of achieving power conversion efficiencies of 6.0% and IQE ≈ 90%, despite the fact that the polymer triplet state lies 300 meV below the interfacial CT state. However, as we push the open circuit voltage (V(OC)) higher by tailoring the fullerene reduction potential, we observe signatures of a new recombination loss process near V(OC) = 1.0 V that we do not observe for PCBM-based devices. Using photoinduced absorption and photoluminescence spectroscopy, we show that a new recombination path opens via the fullerene triplet manifold as the energy of the lowest CT state approaches the energy of the fullerene triplet. This pathway appears active even in cases where direct recombination via the polymer triplet remains thermodynamically accessible. These results suggest that kinetics, as opposed to thermodynamics, can dominate recombination via triplet excitons in these blends and that optimization of charge separation and kinetic suppression of charge recombination may be fruitful paths for the next generation of panchromatic organic solar cell materials with high V(OC) and J(SC).

Solution processed inverted tandem polymer solar cells with self-assembled monolayer modified interfacial layers

Inverted tandem bulk-heterojunction solar cells with comparable efficiency to single layer devices have been demonstrated by utilizing two thin layers (∼50 nm) of poly-(3-hexylthiophene):[6,6]-phenyl C61 butyric acid methyl ester as the active material and a fullerene self-assembled monolayer (C60-SAM) to modify the interfaces between the ZnO buffer layer and the active layer. Single and tandem solar cells without the SAM modification have much lower efficiencies than the ones with modification. The successful demonstrations of inverted tandem devices with SAM modification give promise of further device improvements if active materials with complementary absorption can be used.