3 research outputs found
Facile Method toward Hierarchical Fullerene Architectures with Enhanced Hydrophobicity and Photoluminescence
A two-step self-assembly strategy
has been developed for the preparation of fullerene hierarchical architectures.
Typically, the precipitation method is utilized to synthesize the
initial fullerene microstructures, and subsequently a drop-drying
process is employed to facilitate the fullerene microstructures to
self-assemble into the final hierarchical structures. Overall, this
methodology is quite simple and feasible, which can be applied to
prepare fullerene hierarchical structures with different morphological
features, simply by choosing proper solvent. Moreover, the as-obtained
C<sub>70</sub> hierarchical structures have many superior properties
over the original C<sub>70</sub> microrods such as superhydrophobicity
and unique photoluminescence behaviors, promising their applications
as waterproof optoelectronics
Lu<sub>2</sub>@C<sub>82</sub> Nanorods with Enhanced Photoluminescence and Photoelectrochemical Properties
One-dimensional
(1D) single-crystalline hexagonal nanorods of Lu<sub>2</sub>@<i>C</i><sub>3<i>v</i></sub>(8)–C<sub>82</sub> were prepared for the first time using the liquid–liquid
interface precipitation (LLIP) method from the interfaces between
carbon disulfide (CS<sub>2</sub>) and isopropyl alcohol (IPA). The
length of the nanorods can be readily controlled by varying the concentration
of the Lu<sub>2</sub>@C<sub>82</sub> solution in addition to the volume
ratio of CS<sub>2</sub> to IPA. The latter factor also exhibits a
significant influence on the morphology of the crystals. The crystalline
structure of the nanorods has been investigated by XRD and selected
area electron diffraction (SAED), suggesting a face-centered cubic
structure. Photoluminescence of the Lu<sub>2</sub>@C<sub>82</sub> nanorods
shows a remarkable enhancement as compared to that of pristine Lu<sub>2</sub>@C<sub>82</sub> powder because of the high crystallinity.
Furthermore, we have investigated the photoelectrochemical properties
of Lu<sub>2</sub>@C<sub>82</sub> nanorods, proving their potential
applications as photodetectors
Understanding Charge-Transfer Characteristics in Crystalline Nanosheets of Fullerene/(Metallo)porphyrin Cocrystals
Cocrystals
in the form of crystalline nanosheets comprised of C<sub>70</sub> and
(metallo)Âporphyrins were prepared by using the liquid–liquid
interfacial precipitation (LLIP) method where full control over the
morphologies in the C<sub>70</sub>/(metallo)Âporphyrins nanosheets
has been accomplished by changing the solvent and the relative molar
ratio of fullerene to (metallo)Âporphyrin. Importantly, the synergy
of integrating C<sub>70</sub> and (metallo)Âporphyrins as electron
acceptors and donors, respectively, into nanosheets is substantiated
in the form of a near-infrared charge-transfer absorption. The presence
of the latter, as reflection of ground-state electron donor–acceptor
interactions in the nanosheets, in which a sizable redistribution
of charge density from the electron-donating (metallo)Âporphyrins to
the electron-accepting C<sub>70</sub> occurs, leads to a quantitative
quenching of the localized (metallo)Âporphyrin fluorescence. Going
beyond the ground-state characterization, excited-state electron donor–acceptor
interactions are the preclusion to a full charge transfer featuring
formation of a radical ion pair state, that is, the one-electron reduced
fullerene and the one-electron oxidized (metallo)Âporphyrin