Transition-metal nanoparticles possess unique size-dependent optical, electronic, and catalytic properties on the nanoscale, which differ significantly from their bulk properties. In particular, palladium (Pd) nanoparticles have properties applicable to a wide range of applications in catalysis and electronics. However, predictable and controllable nanoparticle synthesis remains challenging because of harsh reaction conditions, artifacts from capping agents, and unpredictable growth. Biological supramolecules offer attractive templates for nanoparticle synthesis because of their precise structure and size. In this article, we demonstrate simple, controllable Pd nanoparticle synthesis on surface-assembled viral nanotemplates. Specifically, we exploit precisely spaced thiol functionalities of genetically modified tobacco mosaic virus (TMV1cys) for facile surface assembly and readily controllable Pd nanoparticle synthesis via simple electroless deposition under mild aqueous conditions. Atomic force microscopy (AFM) studies clearly show tunable surface assembly and Pd nanoparticle formation preferentially on the TMV1cys templates. Grazing incidence small-angle X-ray scattering (GISAXS) further provided an accurate and statistically meaningful route by which to investigate the broad size ranges and uniformity of the Pd nanoparticles formed on TMV templates by simply tuning the reducer concentration. We believe that our viral-templated bottom-up approach to tunable Pd nanoparticle formation combined with the first in-depth characterization via GISAXS represents a major advancement toward exploiting viral templates for facile nanomaterials/device fabrication. We envision that our strategy can be extended to a wide range of applications, including uniform nanostructure and nanocatalyst synthesis.
Photosystem I (PSI) is a key component of oxygenic photosynthetic electron transport because of its light-induced electron transfer to the soluble electron acceptor ferredoxin. This work demonstrates the incorporation of surface assembled cyanobacterial trimeric PSI complexes into a biohybrid system for light-driven current generation. Specifically, this work demonstrates the improved assembly of PSI via electrophoretic deposition, with controllable surface assembled PSI density, on different self-assembled alkanethiol monolayers. Using artificial electron donors and acceptors (Os(bpy)(2)Cl(2) and methyl viologen) we demonstrate photocurrent generation from a single PSI layer, which remains photoactive for at least three hours of intermittent illumination. Photoelectrochemical comparison of the biohybrid systems assembled from different alkanethiols (hexanethiol, aminohexanethiol, mercaptohexanol, and mercaptohexanoic acid) reveals that the PSI generated photocurrent is enhanced by almost 5 times on negatively charged SAM surfaces as compared to positively charged surfaces. These results are discussed in light of how PSI is oriented upon electrodeposition on a SAM.
We demonstrate rapid microfluidic fabrication of hybrid microparticles composed of functionalized viral nanotemplates directly embedded in polymeric hydrogels. Specifically, genetically modified tobacco mosaic virus (TMV) templates were covalently labeled with fluorescent markers or metalized with palladium (Pd) nanoparticles (Pd-TMV), then suspended in a poly(ethylene glycol)-based solution. Upon formation in a flow-focusing device, droplets were photopolymerized with UV light to form microparticles. Fluorescence and confocal microscopy images of microparticles containing fluorescently labeled TMV show uniform distribution of TMV nanotemplates throughout the microparticles. Catalytic activity, via the dichromate reduction reaction, is also demonstrated with microparticles containing Pd-TMV complexes. Additionally, Janus microparticles were fabricated containing viruses embedded in one side and magnetic nanoparticles in the other, that enabled simple separation from bulk solution. These results represent a facile route to directly harness the advantages of viral nanotemplates into a readily usable and stable 3D assembled format.
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