2021
DOI: 10.1016/j.surfin.2021.101058
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Growth, morphology and molecular orientation of controlled Indigo thin films on silica surfaces

Abstract: del Risorgimento, 4 -40136 Bologna (Italy) [b] Consiglio Nazionale delle Ricerche -Istituto per lo Studio dei Materiali Nanostrutturati (CNR-ISMN) via P. Gobetti 101, 40129 Bologna, Italy [c] Consiglio Nazionale delle Ricerche -Istituto per la Microelettronica e i Microsistemi (CNR-IMM) via P.

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Cited by 7 publications
(7 citation statements)
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References 63 publications
(90 reference statements)
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“…Similarly, vapor films grown on various substrates [100] displayed a sharp single diffraction peak, which was taken as an indication of a crystalline texture with a preferential orientation, without however reporting to which polymorph it should be attributed. The issue has been clarified with the help of low-wavenumber Raman spectroscopy in a recent work [101] which provides new insight on the molecular arrangement of indigo on the substrate via the employment of a combination of techniques, confirming the key role of the extended network of intermolecular H-bonds in the growth of these systems. Figure 8 displays the AFM morphologies of three indigo films deposited in ultra-high vacuum conditions on Si/SiO 2 at different evaporation rates (10, 70 and 200 ng/min), alongside with their specular X-ray and Raman spectra.…”
Section: Indigo High-vacuum Evaporated Films and Their Phase Composition Questionmentioning
confidence: 99%
“…Similarly, vapor films grown on various substrates [100] displayed a sharp single diffraction peak, which was taken as an indication of a crystalline texture with a preferential orientation, without however reporting to which polymorph it should be attributed. The issue has been clarified with the help of low-wavenumber Raman spectroscopy in a recent work [101] which provides new insight on the molecular arrangement of indigo on the substrate via the employment of a combination of techniques, confirming the key role of the extended network of intermolecular H-bonds in the growth of these systems. Figure 8 displays the AFM morphologies of three indigo films deposited in ultra-high vacuum conditions on Si/SiO 2 at different evaporation rates (10, 70 and 200 ng/min), alongside with their specular X-ray and Raman spectra.…”
Section: Indigo High-vacuum Evaporated Films and Their Phase Composition Questionmentioning
confidence: 99%
“…116 Since then significant efforts towards incorporating indigo in the organic electronics have emerged. 115,[117][118][119][120][121][122][123][124][125][126][127][128][129][130] Indigo has exhibited very promising semiconducting behaviors. It has balanced ambipolar charge transport, stemming from its reversible redox states and displays good charge mobility (1 Â 10 À2 cm 2 V À1 s À1 ).…”
Section: Indigomentioning
confidence: 99%
“…115,117,118 Indigo thin films have been extensively used in OFET devices, organic inverters, and photodiode as active layers. [117][118][119][120][121] Indigo is electronic deficient and has been used as an non-fullerene acceptor in blends with the donor P3HT for use in OPVs. 122 Besides acting as a small molecule semiconductor itself, indigo is also an electron accepting building block in semiconducting D-A copolymers.…”
Section: Indigomentioning
confidence: 99%
“…14 All elements of the class also exhibit extended polymorphism, with phases which are metastable in the processing conditions getting stabilized at surface growths or forming genuine thin film phases. [11][12][13]15,16 Among other pigment candidates as semiconductors, quinacridone (QA) has the peculiarity of possessing a molecular structure appearing like that of OSC pentacene, 17 where however the p conjugation on the molecular skeleton is broken by the substituents on the rings. Thus, similar to the case of indigo, 15 the solid-state assembly is driven both by the very strong intermolecular H-bonds due to the substituents and by the p stacking of neighboring molecules.…”
Section: Introductionmentioning
confidence: 99%
“…[11][12][13]15,16 Among other pigment candidates as semiconductors, quinacridone (QA) has the peculiarity of possessing a molecular structure appearing like that of OSC pentacene, 17 where however the p conjugation on the molecular skeleton is broken by the substituents on the rings. Thus, similar to the case of indigo, 15 the solid-state assembly is driven both by the very strong intermolecular H-bonds due to the substituents and by the p stacking of neighboring molecules. The interplay of interactions results for QA in the existence of four known polymorphs.…”
Section: Introductionmentioning
confidence: 99%