Yongli Yan

Two-photon pumped lasing in single-crystal organic nanowire exciton polariton resonators.

Single-crystal organic nanowires were fabricated with a soft-template-assisted self-assembly method in liquid phase. These nanowires with rectangular cross section can serve as resonators for exciton-photon coupling, leading to a microcavity effect and a relatively low threshold of laser actions. Two-photon-pumped blue lasing was observed in these organic waveguiding nanostructures above a threshold of 60 nJ, excited with a 750 nm near-infrared femtosecond pulse laser at 77 K.

Wire-on-Wire Growth of Fluorescent Organic Heterojunctions

Dendritic organic heterojunctions with aluminum tris(8-hydroxyquinoline) (Alq(3)) microwire trunks and 1,5-diaminoanthraquinone (DAAQ) nanowire branches were prepared by a two-step growth process. The prefabricated Alq(3) microwires act as nucleation centers for site-specific secondary vapor growth of DAAQ nanowires, resulting in the unique dendritic heterostructures. When the trunk was excited with a focused laser beam, emitted light of various colors was simultaneously channeled from the branched nanowires via both waveguiding and energy transfer. The intensity of the out-coupled emissions was modulated effectively by changing the polarization of the incident light.

Low‐Threshold Wavelength‐Switchable Organic Nanowire Lasers Based on Excited‐State Intramolecular Proton Transfer

Coherent light signals generated at the nanoscale are crucial to the realization of photonic integrated circuits. Self-assembled nanowires from organic dyes can provide both a gain medium and an effective resonant cavity, which have been utilized for fulfilling miniaturized lasers. Excited-state intramolecular proton transfer (ESIPT), a classical molecular photoisomerization process, can be used to build a typical four-level system, which is more favorable for population inversion. Low-power driven lasing in proton-transfer molecular nanowires with an optimized ESIPT energy-level process has been achieved. With high gain and low loss from the ESIPT, the wires can be applied as effective FP-type resonators, which generated single-mode lasing with a very low threshold. The lasing wavelength can be reversibly switched based on a conformation conversion of the excited keto form in the ESIPT process.

New Electron-Donor/Acceptor-Substituted Tetraphenylethylenes: Aggregation-Induced Emission with Tunable Emission Color and Optical-Waveguide Behavior

Herein, we report the synthesis of new tetraphenylethylene derivatives 1-5 that feature electron-donating (methoxy) and -accepting (dicyanomethane) groups as AIE-active molecules with tunable emission colors. The crystal structures of compounds 3 and 4 are described and the intermolecular interactions within their crystals agree with the observation that they exhibit strong solid-state emission. Compounds 1-4 exhibit typical AIE behavior and their emission maxima are red-shifted in the order: 1<2<3<4. Such red-shifts are ascribed to the fact that intramolecular interactions between the electron donor and the electron acceptor become stronger with increasing number of methoxy groups. The solid-state emission colors of compounds 1-4 are successfully tuned from yellow-green to red. Compound 5 shows AIE behavior, but its emission is only slightly enhanced after aggregation and its solid shows a low quantum yield. Furthermore, microplates of compound 3 exhibit 2D optical-waveguide behavior.

Highly Solid-State Emissive Pyridinium-Substituted Tetraphenylethylene Salts: Emission Color-Tuning with Counter Anions and Application for Optical Waveguides

In this paper seven salts of pyridinium-substituted tetraphenylethylene with different anions are reported. They show typical aggregation-induced emission. Crystal structures of three of the salts with (CF(3)SO(2))(2) N(-), CF(3) SO(3)(-), and SbF(6)(-) as the respective counter anions, are determined. The emission behavior of their amorphous and crystalline solids is investigated. Both amorphous and crystalline solids, except for the one with I(-), are highly emissive. Certain amorphous solids are red-emissive with almost the same quantum yields and fluorescence life-times. However, some crystalline solids are found to show different emission colors varying from green to yellow. Thus, their emission colors can be tuned by the counter anions. Furthermore, certain crystalline solids are highly emissive compared to the respective amorphous solids. Such solid-state emission behavior of these pyridinium-substituted tetraphenylethylene salts is interpreted on the basis of their crystal structures. In addition, optical waveguiding behavior of fabricated microrods is presented.

Recent Advances in Organic One‐Dimensional Composite Materials: Design, Construction, and Photonic Elements for Information Processing

Many recent activities in the use of one-dimensional nanostructures as photonic elements for optical information processing are explained by huge advantages that photonic circuits possess over traditional silicon-based electronic ones in bandwidth, heat dissipation, and resistance to electromagnetic wave interference. Organic materials are a promising candidate to support these optical-related applications, as they combine the properties of plastics with broad spectral tunability, high optical cross-section, easy fabrication, as well as low cost. Their outstanding compatibility allows organic composite structures which are made of two or more kinds of materials combined together, showing great superiority to single-component materials due to the introduced interactions among multiple constituents, such as energy transfer, electron transfer, exciton coupling, etc. The easy processability of organic 1D crystalline heterostructures enables a fine topological control of both composition and geometry, which offsets the intrinsic deficiencies of individual material. At the same time, the strong exciton-photon coupling and exciton-exciton interaction impart the excellent confinement of photons in organic microstructures, thus light can be manipulated according to our intention to realize specific functions. These collective properties indicate a potential utility of organic heterogeneous material for miniaturized photonic circuitry. Herein, focus is given on recent advances of 1D organic crystalline heterostructures, with special emphasis on the novel design, controllable construction, diverse performance, as well as wide applications in isolated photonic elements for integration. It is proposed that the highly coupled, hybrid optical networks would be an important material basis towards the creation of on-chip optical information processing.

Optical Modulation Based on Direct Photon‐Plasmon Coupling in Organic/Metal Nanowire Heterojunctions

Surface plasmon polaritons (SPPs) can be launched with an organic nanowire that serves as both light source and dielectric waveguide in a single organic/metal nanowire heterojunction. Efficient modulation of the output signals from the silver tip can be achieved via the alternation of incident polarizations, which is further used to design and realize prototypical photonic-plasmonic logic devices. These findings are essential for incorporating plasmonic waveguides as practical components into hybrid high-capacity photonic circuits.

From Molecular Design and Materials Construction to Organic Nanophotonic Devices

CONSPECTUS: Nanophotonics has recently received broad research interest, since it may provide an alternative opportunity to overcome the fundamental limitations in electronic circuits. Diverse optical materials down to the wavelength scale are required to develop nanophotonic devices, including functional components for light emission, transmission, and detection. During the past decade, the chemists have made their own contributions to this interdisciplinary field, especially from the controlled fabrication of nanophotonic molecules and materials. In this context, organic micro- or nanocrystals have been developed as a very promising kind of building block in the construction of novel units for integrated nanophotonics, mainly due to the great versatility in organic molecular structures and their flexibility for the subsequent processing. Following the pioneering works on organic nanolasers and optical waveguides, the organic nanophotonic materials and devices have attracted increasing interest and developed rapidly during the past few years. In this Account, we review our research on the photonic performance of molecular micro- or nanostructures and the latest breakthroughs toward organic nanophotonic devices. Overall, the versatile features of organic materials are highlighted, because they brings tunable optical properties based on molecular design, size-dependent light confinement in low-dimensional structures, and various device geometries for nanophotonic integration. The molecular diversity enables abundant optical transitions in conjugated π-electron systems, and thus brings specific photonic functions into molecular aggregates. The morphology of these micro- or nanostructures can be further controlled based on the weak intermolecular interactions during molecular assembly process, making the aggregates show photon confinement or light guiding properties as nanophotonic materials. By adoption of some active processes in the composite of two or more materials, such as energy transfer, charge separation, and exciton-plasmon coupling, a series of novel nanophotonic devices could be achieved for light signal manipulation. First, we provide an overview of the research evolution of organic nanophotonics, which arises from attempts to explore the photonic potentials of low-dimensional structures assembled from organic molecules. Then, recent advances in this field are described from the viewpoints of molecules, materials, and devices. Many kinds of optofunctional molecules are designed and synthesized according to the demands in high luminescence yield, nonlinear optical response, and other optical properties. Due to the weak interactions between these molecules, numerous micro- or nanostructures could be prepared via self-assembly or vapor-deposition, bringing the capabilities of light transport and confinement at the wavelength scale. The above advantages provide great possibilities in the fabrication of organic nanophotonic devices, by rationally combining these functional components to manipulate light signals. Finally, we present our views on the current challenges as well as the future development of organic nanophotonic materials and devices. This Account gives a comprehensive understanding of organic nanophotonics, including the design and fabrication of organic micro- or nanocrystals with specific photonic properties and their promising applications in functional nanophotonic components and integrated circuits.

Electrogenerated Chemiluminescence of Metal–Organic Complex Nanowires: Reduced Graphene Oxide Enhancement and Biosensing Application

Electrogenerated chemiluminescence (ECL) is the production of light from the high-energy electron-transfer reaction between electrogenerated species. [ 1 ] As a valuable detection method, ECL is becoming more recognized in analytical chemistry due to its versatility, high stability, low background signal, and good temporal and spatial control. [ 2–5 ] Regenerable ECL sensors have been extensively studied, because they can reduce the consumption of reagents and simplify the experimental design. [ 6–12 ]

One‐Dimensional Organic Photonic Heterostructures: Rational Construction and Spatial Engineering of Excitonic Emission

Organic photonic heterostructures are constructed through a template-free self-assembly method. The host-guest intermolecular interactions play an essential role in the formation of various block orange-blue-orange and blue/green microtubes. The spatial distribution of excitons is engineered to investigate the excitonic behaviors in light propagation along the axial heterostructures. These results offer a new route to the integration of organic photonic building blocks for optical processing applications.