Yuebing Zheng

Visibly transparent polymer solar cells produced by solution processing.

Visibly transparent photovoltaic devices can open photovoltaic applications in many areas, such as building-integrated photovoltaics or integrated photovoltaic chargers for portable electronics. We demonstrate high-performance, visibly transparent polymer solar cells fabricated via solution processing. The photoactive layer of these visibly transparent polymer solar cells harvests solar energy from the near-infrared region while being less sensitive to visible photons. The top transparent electrode employs a highly transparent silver nanowire-metal oxide composite conducting film, which is coated through mild solution processes. With this combination, we have achieved 4% power-conversion efficiency for solution-processed and visibly transparent polymer solar cells. The optimized devices have a maximum transparency of 66% at 550 nm.

Fused Silver Nanowires with Metal Oxide Nanoparticles and Organic Polymers for Highly Transparent Conductors

Silver nanowire (AgNW) networks are promising candidates to replace indium-tin-oxide (ITO) as transparent conductors. However, complicated treatments are often required to fuse crossed AgNWs to achieve low resistance and good substrate adhesion. In this work, we demonstrate a simple and effective solution method to achieve highly conductive AgNW composite films with excellent optical transparency and mechanical properties. These properties are achieved via sequentially applying TiO(2) sol-gel and PEDOT:PSS solution to treat the AgNW film. TiO(2) solution volume shrinkage and the capillary force induced by solvent evaporation result in tighter contact between crossed AgNWs and improved film conductivity. The PEDOT:PSS coating acts as a protecting layer to achieve strong adhesion. Organic photovoltaic devices based on the AgNW-TiO(2)-PEDOT:PSS transparent conductor have shown comparable performance to those based on commercial ITO substrates.

Viologen-Mediated Assembly of and Sensing with Carboxylatopillar[5]arene-Modified Gold Nanoparticles

Carboxylatopillar[5]arene (CP[5]A), a new water-soluble macrocyclic synthetic receptor, has been employed as a stabilizing ligand for in situ preparation of gold nanoparticles (AuNPs) to gain new insights into supramolecular host-AuNP interactions. CP[5]A-modified AuNPs with good dispersion and narrow size distributions (3.1 ± 0.5 nm) were successfully produced in aqueous solution, suggesting a green synthetic pathway for the application of AuNPs in biological systems. Supramolecular self-assembly of CP[5]A-modified AuNPs mediated by suitable guest molecules was also investigated, indicating that the new hybrid material is useful for sensing and detection of the herbicide paraquat.

Systematic investigation of localized surface plasmon resonance of long-range ordered Au nanodisk arrays

Ordered Au nanodisk arrays were fabricated on glass substrates using nanosphere lithography combined with a two-step reactive ion etching technique. The optical properties of these arrays were investigated both experimentally and theoretically. Specifically, the effects of disk diameter on localized surface plasmon resonance (LSPR) were characterized and compared with results from discrete dipole approximation (DDA) calculations. The effects of glass substrate, Cr interfacial layer, and Au thickness on LSPR were investigated computationally. Furthermore, thermal treatment was found to be essential in improving the nanodisk arrays’ LSPR properties. Using atomic force microscopy and DDA calculations, it was established that the improvements in LSPR properties were due to thermally induced morphologic changes. Finally, microfluidic channels were integrated with the annealed disk arrays to study the sensitivity of LSPR to the change in surroundings’ refractive index. The dependence of LSPR on surroundings’ refractive index was measured and compared with calculated results.

Molecular plasmonics for biology and nanomedicine

The optical excitation of surface plasmons in metal nanoparticles leads to nanoscale spatial confinement of electromagnetic fields. The confined electromagnetic fields can generate intense, localized thermal energy and large near-field optical forces. The interaction between these effects and nearby molecules has led to the emerging field known as molecular plasmonics. Recent advances in molecular plasmonics have enabled novel optical materials and devices with applications in biology and nanomedicine. In this article, we categorize three main types of interactions between molecules and surface plasmons: optical, thermal and mechanical. Within the scope of each type of interaction, we will review applications of molecular plasmonics in biology and nanomedicine. We include a wide range of applications that involve sensing, spectral analysis, imaging, delivery, manipulation and heating of molecules, biomolecules or cells using plasmonic effects. We also briefly describe the physical principles of molecular plasmonics and progress in the nanofabrication, surface functionalization and bioconjugation of metal nanoparticles.

Surface-Enhanced Raman Spectroscopy to Probe Reversibly Photoswitchable Azobenzene in Controlled Nanoscale Environments

We apply in situ surface-enhanced Raman spectroscopy (SERS) to probe the reversible photoswitching of azobenzene-functionalized molecules inserted in self-assembled monolayers that serve as controlled nanoscale environments. Nanohole arrays are fabricated in Au thin films to enable SERS measurements associated with excitation of surface plasmons. A series of SERS spectra are recorded for azobenzene upon cycling exposure to UV (365 nm) and blue (450 nm) light. Experimental spectra match theoretical calculations. On the basis of both the simulations and the experimental data analysis, SERS provides quantitative information on the reversible photoswitching of azobenzene in controlled nanoscale environments.

Molecular Switches and Motors on Surfaces

Molecular switches and motors respond structurally, electronically, optically, and/or mechanically to external stimuli, testing and potentially enabling extreme miniaturization of optoelectronic devices, nanoelectromechanical systems, and medical devices. The assembly of motors and switches on surfaces makes it possible both to measure the properties of individual molecules as they relate to their environment and to couple function between assembled molecules. In this review, we discuss recent progress in assembling molecular switches and motors on surfaces, measuring static and dynamic structures, understanding switching mechanisms, and constructing functional molecular materials and devices. As demonstrative examples, we choose a representative molecule from three commonly studied classes including molecular switches, photochromic molecules, and mechanically interlocked molecules. We conclude by offering perspectives on the future of molecular switches and motors on surfaces.

Aminopropyltriethoxysilane (APTES)-functionalized nanoporous polymeric gratings: fabrication and application in biosensing

We have fabricated aminopropyltriethoxysilane (APTES)-functionalized nanoporous polymeric gratings by combining holographic interference patterning and APTES-functionalization of the pre-polymer syrup. The APTES facilitates the immobilization of biomolecules onto the polymeric grating surfaces. The successful detection of multiple biomolecules (biotin, steptavidin, biotinylated anti-rabbit IgG, and rabbit-IgG) indicates that the functionalized nanoporous polymeric gratings can act as biosensing platforms which are label-free, inexpensive, and applicable as high-throughput assays.

Optically switchable gratings based on azo-dye-doped, polymer-dispersed liquid crystals

We report a holographically fabricated, optically switchable grating using azo-dye-doped, polymer-dispersed liquid crystals (LCs). Our experiments show that upon photoirradiation, the diffraction of the grating was decreased significantly. We believe that this switching behavior is due to two factors--nematic-isotropic phase transition of LCs and thermal expansion of the grating structure.

Dynamic Tuning of Plasmon–Exciton Coupling in Arrays of Nanodisk–J‐aggregate Complexes

Y.B.Z and B.K.J contributed equally to this work. This research was supported by the Air Force Office of Scientific Research (FA9550-08-1-0349), the National Science Foundation (ECCS-0801922, ECCS-0609128, and ECCS-0609128), and the Penn State Center for Nanoscale Science (MRSEC). Components of this work were conducted at the Pennsylvania State University node of the NSF-funded National Nanotechnology Infrastructure Network. Y.B.Z. recognizes the support from KAUST Scholar Award and the Founders Prize and Grant of the American Academy of Mechanics. The authors thank I-Kao Chiang, Aitan Lawit and Thomas R. Walker for helpful discussions.