2022
DOI: 10.1016/j.orgel.2022.106448
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Manipulate organic crystal morphology and charge transport

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Cited by 28 publications
(20 citation statements)
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“…[4][5][6][7] At the same time, many efforts have been made to enhance the charge transport properties of small molecules that play a crucial role in improving device performance. 8,9 Charge carrier mobility (m) is strongly related to the crystallinity of materials, and the microstructure and morphology of thin films. 10,11 Many amorphous organic semiconductors show low charge mobilities in the range of 10 À5 -10 À3 cm 2 V À1 s À1 , while m values of highly crystalline small molecules can exceed 10 cm 2 V À1 s À1 .…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…[4][5][6][7] At the same time, many efforts have been made to enhance the charge transport properties of small molecules that play a crucial role in improving device performance. 8,9 Charge carrier mobility (m) is strongly related to the crystallinity of materials, and the microstructure and morphology of thin films. 10,11 Many amorphous organic semiconductors show low charge mobilities in the range of 10 À5 -10 À3 cm 2 V À1 s À1 , while m values of highly crystalline small molecules can exceed 10 cm 2 V À1 s À1 .…”
Section: Introductionmentioning
confidence: 99%
“…10,11 Many amorphous organic semiconductors show low charge mobilities in the range of 10 À5 -10 À3 cm 2 V À1 s À1 , while m values of highly crystalline small molecules can exceed 10 cm 2 V À1 s À1 . 8 Unfortunately, the synthesis and purification of highly crystalline p-conjugated molecules as well as growth of single-crystals are difficult. Moreover, the poor solubility of crystalline materials in common organic solvents hinders the fabrication of electronic devices by high-throughput printing technologies.…”
Section: Introductionmentioning
confidence: 99%
“…For example, TIPS pentacene, when deposited via the method of drop casting, can exhibit dendritic structures of morphology with each organic crystal pointing in different directions. [44][45][46][47][48][49] The organic semiconductor 5,6,11,12-tetrachlorotetracene was also reported to exhibit multiple layers of misoriented wires stacking upon one another. 50 The 2,5-di-(2-ethylhexyl)-3,6-bis(5 00 -n-hexyl-2,2 0 , 5 0 ,2 00 ]terthiophen-5-yl)-pyrrolo [3,4-c]pyrrole-1,4-dione (SMDPPEH) semiconductor from drop casting in a single solvent showed star-shaped organic crystals while a majority of semiconductors formed aggregations on the substrate without full crystallization.…”
Section: Background and Challengesmentioning
confidence: 99%
“…In the solution-based techniques, external forcebased, additive-based, and binary solvent-based techniques are often employed to drive a sequential self-assembly of the molecular solutes in each pattern unit. [27,28] This gradient crystallization exerted by external forces is also helpful to align the inter-pattern orientation to some extent; however, realizing homogeneous orientation among all the isolated pattern units is still a hard task. Likewise, vapor growth of patterns constituted of discrete anisotropic single crystals is essentially different with deposition of the isotropic amorphous or polycrystalline patterns; in the latter process one need not to concern about control of the crystallographic orientation but only to confine the deposition positions.…”
Section: Introductionmentioning
confidence: 99%