2019
DOI: 10.1021/acsami.9b02090
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Control over Tuning Fullerene Microcrystals by Means of Engineering Charge-Transfer Interactions

Abstract: Multifunctional fullerene microcrystals have been prepared by the instruction of water in the liquidliquid interfacial precipitation. The resulting microcrystals were characterized microscopically and spectroscopically. The role of water in engineering charge transfer interactions between fullerenes and electron donating solvents have been corroborated through thermogravimetric and transient absorption spectroscopy analysis.

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Cited by 5 publications
(5 citation statements)
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“…For example, the activation/deactivation of charge‐transfer interactions between Y@C 82 /NiP is dominated by solvents used for the co‐crystallization due to the solvent‐dependent crystallographic packing in the co‐crystals. [ 25 ] Similar observations have also been demonstrated in C 60 /NMP FMNAs [ 67 ] and the Sc 3 N@C 80 /ZnTPyP system, [ 124 ] where the incorporation of water or surfactant CTAB modulates charge‐transfer interactions in both the ground and excited states. In addition to these above‐mentioned factors, the wetting of substrates could also affect the formation of well‐aligned C 60 ribbons and the electron mobility of the field‐effect transistor device.…”
Section: Properties Modulation and Emerging Applications Of Fmnassupporting
confidence: 63%
See 1 more Smart Citation
“…For example, the activation/deactivation of charge‐transfer interactions between Y@C 82 /NiP is dominated by solvents used for the co‐crystallization due to the solvent‐dependent crystallographic packing in the co‐crystals. [ 25 ] Similar observations have also been demonstrated in C 60 /NMP FMNAs [ 67 ] and the Sc 3 N@C 80 /ZnTPyP system, [ 124 ] where the incorporation of water or surfactant CTAB modulates charge‐transfer interactions in both the ground and excited states. In addition to these above‐mentioned factors, the wetting of substrates could also affect the formation of well‐aligned C 60 ribbons and the electron mobility of the field‐effect transistor device.…”
Section: Properties Modulation and Emerging Applications Of Fmnassupporting
confidence: 63%
“…For example, solvent combinations of CCl 4 /IPA, benzene/IPA, benzene/TBA, NMP/IPA, or NMP/IPA/H 2 O guide the generation of C 60 -based hexagonal 2D nanosheets, 1D nanowhiskers, mixed 2D polygons, 1D fibers, or microparticles, respectively (Figure 9). [27,67,75] Moreover, varying the alcohol type from ethanol, 1-propanol, to 1-butanol (as poor solvents) leads to the evolution of the morphologies of the final C 60 -based FMNAs from 3D irregular, 2D (e.g., hexagonal plates), to 1D rod-shaped microcrystals. [76] Interestingly, cyclic transformation of the shape of C 60 microcrystals was achieved by changing the solvents, which led to a change of the as-grown rod-shape to hexagonal disc-shape, then to belt-shape, and back to rod-shape.…”
Section: Solvent Engineeringmentioning
confidence: 99%
“…Fullerenes have also been recognized as good candidates for solid lubricants, due to the unique spherical or ellipsoidal structures, high compressive capacity, weak intermolecular force, and low surface energy . Since the fullerene was first discovered by Kroto et al in 1985 in the process of vaporizing graphite by laser irradiation, the synthesis and property of fullerenes have been widely investigated. With the excellent performance in superconductivity, magnetism, and optics, fullerenes demonstrate great potential to be applied to solar cells, optical devices, drug delivery, and so forth. …”
Section: Introductionmentioning
confidence: 99%
“…The amorphous structure of the heat-treated samples was further confirmed by studying Raman spectra (Figure 2b). The pC 60 crystalline material exhibits several Raman vibration bands (six H g vibrations and two A g vibration bands) [47]. However, molecular rotations of the fullerene molecules are restricted in the self-assembled FE-HS system due to crosslinking of the fullerene and EDA molecules; therefore, most of the Raman bands corresponding to the crystalline fullerene are absent in the spectrum of the FE-HS sample (Figure 2b).…”
Section: Resultsmentioning
confidence: 99%