Single graphene derivative layer as a hole transport in organic solar cells based on PBDB-T:ITIC.

A layer of fluorinated reduced graphene oxide (FrGO), as an alternative hole transport (HTL) in organic solar cells (OSCs) based on a PBDB-T:ITIC active layer, is reported. OSC configuration is ITO/HTL/PBDB-T:ITIC/PFN/FM; FM is Field's metal, a eutectic alloy deposited at room atmosphere. PEDOT:PSS, FrGO/PEDOT:PSS, and FrGO are tested as HTLs; the average efficiencies of 8.8, 8.2, and 5.3%, respectively, are reached. Inhomogeneity of the FrGO layer is determined as the main factor that affects the photovoltaic behavior and stability. Device stability is very acceptable, sometimes with a superior behavior than data previously reported; FM also could potentially contribute to this enhanced stability.

Scanning Probe Microscopy Analysis of Nonfullerene Organic Solar Cells.

In this work, scanning probe microscopies (SPMs) are used for the analysis of PBDB-T, ITIC, and PBDB-T:ITIC layers of solar cells (OSCs). Scanning tunneling microscopy (STM) images of PBDB-T reveal that thin films (<1 nm) tend to form worm-like pattern (amorphous type) domains with an average chain-to-chain distance of 950 pm; likewise, STM images of ITIC show that side arms form chain-like patterns. STM images of PBDB-T:ITIC blend suggest why PBDB-T domains could facilitate charge dissociation. Further, a strong interchain π-π interaction of the ITIC molecules could promote self-organization, and under the mutual interaction with the PBDB-T polymer, it could influence the pathway formation for electron transport. Moreover, when correlating electrostatic force microscopy (EFM) and photoconductive atomic force microscopy (pc-AFM), the blend morphology and its electrical/electronic properties are determined; the ideal domain size of PBDB-T:ITIC blend phases for maximizing the generated photocurrent is 15-35 nm. Furthermore, phase contrast and surface electric potential characteristics with Kelvin probe force microscopy (KPFM) are measured to examine additional details about the surface and potential changes due to the domain differences in the active layer. OSCs based on the nonfullerene PBDB-T:ITIC active layer reach an average power conversion efficiency (PCE) of 9.1% (best 9.2%).

Core carbo-mer of an Extended Tetrathiafulvalene: Redox-Controlled Reversible Conversion to a carbo-Benzenic Dication.

carbo-Benzene is an aromatic molecule devised by inserting C2 units within each C-C bond of the benzene molecule. By integrating the corresponding carbo-quinoid core as bridging unit in a π-extended tetrathiafulvalene (exTTF), it is shown that a carbo-benzene ring can be reversibly formed by electrochemical reduction or oxidation. The so-called carbo-exTTF molecule was thus experimentally prepared and studied by UV-visible absorption spectroscopy and cyclic voltammetry, as well as by X-ray crystallography and by scanning tunneling microscopy (STM) on a surface of highly oriented pyrolytic graphite (HOPG). The molecule and its oxidized and reduced forms were subjected to a computational study at the density functional theory (DFT) level, supporting carbo-aromaticity as a driving force for the formation of the dication, radical cation, and radical anion. By allowing co-planarity of the dithiolylidene rings and carbo-quinoidal core, carbo-exTTFs present a promising new class of redox-active systems.

Interfacial Energetic Level Mapping and Nano-Ordering of Small Molecule/Fullerene Organic Solar Cells by Scanning Tunneling Microscopy and Spectroscopy.

Using scanning tunneling microscopy (STM) and spectroscopy (STS) at the liquid/solid interface, morphology evolution process and energetic level alignment of very thin solid films (thickness: <700 pm), of the low molecular weight molecule DRCN5T and DRCN5T:[70]PCBM blend are analyzed after applying thermal annealing at different temperatures. These films exhibit a worm-like pattern without thermal annealing (amorphous shape); however, after applying thermal annealing at 120 °C, the small molecule film domains crystallize verified by X-ray diffraction: structural geometry becomes a well-defined organized array. By using STS, the energy band diagrams of the semiconductor bulk heterojunction (blended film) at the donor-acceptor interface are determined; morphology and energy characteristics can be correlated with the organic solar cells (OSC) performance. When combining thermal treatment and solvent vapor annealing processes as described in previous literature by using other techniques, OSC devices based on DRCN5T show a very acceptable power conversion efficiency of 9.0%.

Nontoxic pyrite iron sulfide nanocrystals as second electron acceptor in PTB7:PC71BM-based organic photovoltaic cells.

Herein, we report the synthesis of nontoxic pyrite iron sulfide (FeS2) nanocrystals (NCs) using a two-pot method. Moreover, we study the influence of these NCs incorporated into the PTB7:PC71BM active layer of bulk-heterojunction ternary organic photovoltaic (OPV) cells. The OPV devices are fabricated with the direct configuration glass/ITO/PEDOT:PSS/PTB7:PC71BM:FeS2/PFN/FM. The Field's metal (FM) is a eutectic alloy composed of 32.5% Bi, 51% In and 16.5% Sn by weight that melts at 62 °C. It is deposited on the active layer/PFN under atmospheric conditions. Ternary active layers are prepared by adding small amounts of the semiconducting FeS2 NCs at different weight ratios of 0.0, 0.25, 0.5, and 1.0 wt % with respect to the electron donor PTB7. With respect to the reference device (without FeS2), a 21% increase in the power conversion efficiency (PCE) is observed for OPVs with 0.5 wt % FeS2, such that the PCE of the OPVs is enhanced from 5.69 to 6.47%. According to the Kruskal-Wallis and Mann-Whitney statistical tests, all OPV devices follow the same trend.