Core-satellite assemblies of Au@polydopamine@Ag nanoparticles for photothermal-mediated catalytic reaction.

Engineering plasmonic nanoparticles (NPs) into superstructures comprising two or more distinctive materials is highly desirable because these assemblies can unfold new properties that differ from those exhibited by their individual counterparts. In addition, metal NPs such as Au NPs and Ag NPs have played a major role in environmental remediation. In this study, we designed a heterogeneous NP assembly composed of an Au core and Ag satellite by utilizing a mussel-inspired polydopamine (PDA) strategy. This approach afforded substantial enhancement in the catalytic activity because of the synergistic effect between the Au core and Ag satellite. Specifically, the heat from the localized surface plasmon resonance excitation of the Au NPs can accelerate the reduction reaction of 4-nitrophenol, while the Ag NPs act as a catalyst for reducing the activation energy. Overall, we prepared a facile route to produce heterogeneous metal NP assemblies, which offers promise in scalable synthesis and application in heterogeneous catalysis.

Dielectric control of porous polydimethylsiloxane elastomers with Au nanoparticles for enhancing the output performance of triboelectric nanogenerators.

Taking advantage of the triboelectrification effect and electrostatic induction, triboelectric nanogenerators (TENGs) provide a simple and efficient path to convert environmental mechanical energy into electric energy. Since the generation of surface charges and their density on triboelectric materials are the key factors in determining TENG performance, many efforts have been undertaken to engineer the structures and chemistry of triboelectric materials. Among others, dielectric control of triboelectric materials is an emerging approach because the dielectric constant is intimately correlated with the capacitance of materials. In this regard, we prepared porous polydimethylsiloxane (PDMS) composites decorated with Au nanoparticles (NPs), which was designed to engineer the compressibility and dielectric constant of PDMS elastomer. To this end, a polydopamine layer was synthesized on the PDMS surface to facilitate the homogeneous deposition of Au NPs. Unlike untreated PDMS sponges, Au NPs were efficiently coated onto polydopamine-treated PDMS sponges to increase the dielectric constant. When the resulting porous NP-PDMS composites were assembled into TENG devices, the electrical output of the TENGs initially improved but decreased with the amount of Au NPs. This trade-off relationship has been discussed in terms of charge generation on the air surface and pores of NP-PDMS composites based on a recent experimental model.

Metal-enhanced fluorescence in polymer composite films with Au@Ag@SiO2 nanoparticles and InP@ZnS quantum dots.

For white light-emitting diode (LED) applications, semiconductor quantum dots (QDs) have been widely utilized as efficient down-converters to change the blue color of the light source into different emission colors. Because QDs offer spectral tunability over the entire visible light range, as well as improved color purity, they have rapidly replaced conventional phosphor-based white LEDs. However, for the sustainable growth of QD-mediated LEDs, the amount of QDs required must be reduced by enhancing the color-conversion efficiency. For this purpose, we prepared poly(lauryl methacrylate) (PLMA) composite films by the photo-crosslinking polymerization of lauryl methacrylate monomers in the presence of Au@Ag@SiO2 nanoparticles (NPs) and InP@ZnS QDs. In the PLMA composites, the Au@Ag NPs not only amplified the blue light source but also modified the relaxation of the excited QDs via localized surface plasmon resonance. This resulted in a maximum 12.9-fold enhancement in the QD fluorescence. Because the blue light source in this study can be easily replaced by blue LEDs, the enhanced efficiency of QD emissions via the plasmonic effect could potentially increase the performance of QDs for display applications.