Nanoscopic Management of Molecular Packing and Orientation of Small Molecules by a Combination of Linear and Branched Alkyl Side Chains

Authors
Jung, MinwooYoon, YoungwoonPark, Jae HoonCha, WonsukKim, AjeongKang, JinbackGautam, SanjeevSeo, DongkyunCho, Jeong HoKim, HyunjungChoi, Jong YongChae, Keun HwaKwak, KyungwonSon, Hae JungKo, Min JaeKim, HonggonLee, Doh-KwonKim, Jin YoungChoi, Dong HoonKim, BongSoo
Issue Date
2014-06
Publisher
AMER CHEMICAL SOC
Citation
ACS NANO, v.8, no.6, pp.5988 - 6003
Abstract
We synthesized a series of acceptor donor acceptor-type small molecules (SIDPP-EE, SIDPP-EO, SIDPP-OE, and SIDPP-OO) consisting of a dithienosilole (SI) electron-donating moiety and two diketopyrrolopyrrole (DPP) electron-withdrawing moieties each bearing linear n-octyl (O) and/or branched 2-ethylhoryl (E) alkyl side chains. X-ray diffraction patterns revealed that SIDPP-EE and SIDPP-EO films were highly crystalline with pronounced edge-on orientation, whereas SIDPP-OE and SIDPP-OO films were less crystalline with a radial distribution of molecular orientations. Near-edge X-ray absorption fine structure spectroscopy disclosed an edge-on orientation with a molecular backbone tilt angle of similar to 22 degrees for both SIDPP-EE and SIDPP-EO. Our analysis of the molecular packing and orientation indicated that the shorter 2-ethylhexyl groups on the SI core promote tight pi-pi stacking of the molecular backbone, whereas n-octyl groups on the SI core hinder close pi-pi stacking to some degree. Conversely, the longer linear n-octyl groups on the DPP arms facilitate close intermolecular packing via octyl octyl interdigitation. Quantum mechanics/molecular mechanics molecular dynamics simulations determined the optimal three-dimensional positions of the flexible alkyl side chains of the SI and DPP units, which elucidates the structural cause of the molecular packing and orientation explicitly. The alkyl-chain-dependent molecular stacking significantly affected the electrical properties of the molecular films. The edge-on oriented molecules showed high hole mobilities in organic field-effect transistors, while the radially oriented molecules exhibited high photovoltaic properties in organic photovoltaic cells. These results demonstrate that appropriate positioning of alkyl side chains can modulate crystallinity and molecular orientation in SIDPP films, which ultimately have a profound impact on carrier transport and photovoltaic performance.
Keywords
PROCESSED SMALL-MOLECULE; POLYMER SOLAR-CELLS; OLIGOTHIOPHENE DERIVATIVES; FILM MORPHOLOGY; ENERGY-LEVELS; THIN-FILMS; DIKETOPYRROLOPYRROLE; EFFICIENCY; DESIGN; DONOR; PROCESSED SMALL-MOLECULE; POLYMER SOLAR-CELLS; OLIGOTHIOPHENE DERIVATIVES; FILM MORPHOLOGY; ENERGY-LEVELS; THIN-FILMS; DIKETOPYRROLOPYRROLE; EFFICIENCY; DESIGN; DONOR; organic semiconductors; conjugated small molecules; molecular self-assembly; molecular orientation; hole mobility; power conversion efficiency; organic field-effect transistors; organic photovoltaic cells
ISSN
1936-0851
URI
https://pubs.kist.re.kr/handle/201004/126743
DOI
10.1021/nn501133y
Appears in Collections:
KIST Article > 2014
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