A Highly Crystalline Fused‐Ring n‐Type Small Molecule for Non‐Fullerene Acceptor Based Organic Solar Cells and Field‐Effect Transistors
- 13 July 2018
- journal article
- research article
- Published by Wiley in Advanced Functional Materials
- Vol. 28 (35)
Abstract
N‐type organic small molecules (SMs) are attracting attention in the organic electronics field, due to their easy purification procedures with high yield. However, only a few reports show SMs that perform well in both organic field‐effect transistors (OFETs) and organic solar cells (OSCs). Here, the synthesis and characterization of an n‐type small molecule with an indacenodithieno[3,2‐b]thiophene (IDTT) core unit and linear alkylated side chain (C16) (IDTTIC) are reported. Compared to the state‐of‐the‐art n‐type molecule IDTIC, IDTTIC exhibits smaller optical bandgap and higher absorption coefficient, which is due to the enhanced intramolecular effect. After mixing with the polymer donor PBDB‐T, IDTIC‐based solar cells deliver a power conversion efficiency of only 5.67%. In stark contrast, the OSC performance of IDTTIC improves significantly to 11.2%. It is found that the superior photovoltaic properties of PBDB‐T:IDTTIC blends are mainly due to reduced trap‐assisted recombination and enhanced molecular packing coherence length and higher domain purity when compared to IDTIC. Moreover, a significantly higher electron mobility of 0.50 cm2 V−1 s−1 for IDTTIC in OFET devices than for IDTIC (0.15 cm2 V−1 s−1) is obtained. These superior performances in OSCs and OFETs demonstrate that SMs with extended π‐conjugation of the backbone possess a great potential for application in organic electronic devices.Keywords
Funding Information
- King Abdullah University of Science and Technology
- Office of Naval Research Global (N00141512322)
- U.S. Department of Energy (DE‐AC02‐05CH11231)
This publication has 51 references indexed in Scilit:
- Rational Design of Small Molecular Donor for Solution‐Processed Organic Photovoltaics with 8.1% Efficiency and High Fill Factor via Multiple Fluorine Substituents and Thiophene BridgeAdvanced Functional Materials, 2015
- Two-Dimensional π-Expanded Quinoidal Terthiophenes Terminated with Dicyanomethylenes as n-Type Semiconductors for High-Performance Organic Thin-Film TransistorsJournal of the American Chemical Society, 2014
- Imide- and Amide-Functionalized Polymer SemiconductorsChemical Reviews, 2014
- Soft x-ray scattering facility at the Advanced Light Source with real-time data processing and analysisReview of Scientific Instruments, 2012
- Solution-Processed Molecular Bis(Naphthalene Diimide) Derivatives with High Electron MobilityChemistry of Materials, 2011
- Differential Resistance Analysis of Charge Carrier Losses in Organic Bulk Heterojunction Solar Cells: Observing the Transition from Bimolecular to Trap‐Assisted Recombination and Quantifying the Order of RecombinationAdvanced Energy Materials, 2011
- Indacenodithiophene Semiconducting Polymers for High-Performance, Air-Stable TransistorsJournal of the American Chemical Society, 2010
- A high-mobility electron-transporting polymer for printed transistorsNature, 2009
- Experimental determination of the rate law for charge carrier decay in a polythiophene: Fullerene solar cellApplied Physics Letters, 2008
- Effect of traps on the performance of bulk heterojunction organic solar cellsApplied Physics Letters, 2007