Self-assembled monolayers (SAMs) formed from bis(4‘-methylbiphenyl-4-yl) ditelluride (BBPDTe) precursors
on Au(111) and Ag(111) substrates were characterized by high-resolution X-ray photoelectron spectroscopy
and near-edge X-ray absorption fine structure spectroscopy. BBPDTe was found to adsorb dissociatively on
both substrates, resulting in the formation of well-defined, densely packed, and ordered BPTe SAMs, with a
larger molecular inclination, a lower packing density, and inferior crystallinity on Au than on Ag. However,
both BPTe/Au and BPTe/Ag were not stable under ambient conditions but underwent rapid autoxidation,
which affected exclusively the tellurolate headgroups. The BPTe molecules in the oxidized films remained,
however, bound to the substrate by the terminal O atoms coordinated to the Te moieties, and the quality of
the films, given by parameters such as packing density, degree of orientational order, and average tilt angle
of the SAM constituents, was not noticeably affected by the autoxidation. In addition, the BPTe SAMs were
compared with the analogous thiol- and selenol-based systems, and common tendencies for the different
chalcogen headgroups, ranging from Te to O, were derived.
The neural cell adhesion molecule L1 is involved in nervous system development and promotes regeneration in animal models of acute and chronic injury of the adult nervous system. To translate these conducive functions into therapeutic approaches, a 22-mer peptide that encompasses a minimal and functional L1 sequence of the third fibronectin type III domain of murine L1 was identified and conjugated to gold nanoparticles (AuNPs) to obtain constructs that interact homophilically with the extracellular domain of L1 and trigger the cognate beneficial L1-mediated functions. Covalent conjugation was achieved by reacting mixtures of two cysteine-terminated forms of this L1 peptide and thiolated poly(ethylene) glycol (PEG) ligands (~2.1 kDa) with citrate stabilized AuNPs of two different sizes (~14 and 40 nm in diameter). By varying the ratio of the L1 peptide-PEG mixtures, an optimized layer composition was achieved that resulted in the expected homophilic interaction of the AuNPs. These AuNPs were stable as tested over a time period of 30 days in artificial cerebrospinal fluid and interacted with the extracellular domain of L1 on neurons and Schwann cells, as could be shown by using cells from wild-type and L1-deficient mice. In vitro, the L1-derivatized particles promoted neurite outgrowth and survival of neurons from the central and peripheral nervous system and stimulated Schwann cell process formation and proliferation. These observations raise the hope that, in combination with other therapeutic approaches, L1 peptide-functionalized AuNPs may become a useful tool to ameliorate the deficits resulting from acute and chronic injuries of the mammalian nervous system.
An extremely efficient ethanol fuel cell electrode is produced by combining the large surface area of vertically oriented and highly conductive few-layer graphene sheets with electrochemically deposited palladium nanoparticles. The electrodes show an extraordinary high catalyst activity of up to 7977 mA/(mg Pd) at low catalyst loadings of 0.64 µg/cm² and a very high current density of up to 106 mA/cm² at high catalyst loadings of 83 µg/cm². Moreover, the low onset potentials combined with a good poisoning resistance and long-term stability make these electrodes highly suitable for real applications. These features are achieved by using a newly developed electrochemical catalyst deposition process exploiting high voltages of up to 3.5 kV. This technique allows controlling the catalyst amount ranging from a homogeneous widespread distribution of small (≤ 10 nm) palladium nanoparticles to rather dense layers of particles, while every catalyst particle has electrical contact to the graphene electrode.2
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.