Making electrical nanocontacts to nanocrystal assemblies: mapping of room-temperature Coulomb-blockade thresholds in arrays of 28-kDa gold nanocrystals.
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Crystallization↗
Biomedical subjects
Matteo Biancardo
Publications and source records attributed to Matteo Biancardo.
Solid-state photochromic device based on nanocrystalline TiO2 functionalized with electron donor-acceptor species.
In this Communication, we report on a new type of solid-state photochromic device, S-TiO(2)-A, which is based on electron-transfer processes involving a molecular sensitizer (S) and an electron acceptor (A) coadsorbed onto the surface of nanocrystalline TiO(2). The electron-transfer process is mediated by the semiconductor conduction band and leads to a long-lived charge-separated state S(+)/A(-). The lifetime of this state can be controlled by oxygen diffusion through a polymeric coating deposited on the device.
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A potential and ion switched molecular photonic logic gate.
A molecular photonic logic gate is demonstrated by integrating electrical (potential) and chemical (ionic) switching functions into molecules attached at an externally addressable semiconductor substrate.
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Hysteresis of charge tunneling in assemblies of carboxylic acid-modified gold nanoparticles.
We report on charge transport measurements through laterally contacted assemblies of Au nanoparticles capped with 11-mercaptoundecanoic acid ligands. Both alternating- and direct-current data indicate that although the nanoparticles behave as electrically isolated metallic islands, there is a significant influence from the nanoparticle environment, indicating the existence of a slow reorganization process linked to charge transport. On the basis of the observation of temperature-dependent hysteresis of charge tunneling, we propose that this process is due to proton transfer between the carboxylic acid tails of the ligands.
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Novel Ru-dioxolene complexes as potential electrochromic materials and NIR dyes.
A series of Ru(bpy)(2)-dioxolene complexes 1-4 (bpy = 2,2'- bipyridine) and corresponding Ru(dcb)(2)-dioxolene complexes 5-8 (dcbH(2) = 2,2'-bipyridine-4,4'-dicarboxylic acid) have been prepared, and their spectroelectrochemical behavior in solution has been investigated. The complexes show reversible electrochemical behavior accompanied by a strong NIR absorption in their semiquinone forms due to a Ru(dpi) --> sq(pi) MLCT band. Complete quenching of the NIR absorption occurs both upon oxidation (to the quinone form) and upon reduction (to the catechol form) very close to 0 V. The color of the systems can be tuned by using a wide range of ligands. The complexes 5-8 can be anchored onto nanocrystalline inorganic semiconductors allowing incorporation into potential electrochromic devices. As a proof of principle, compound 8 has been adsorbed on nanocrystalline Sb-doped SnO(2) supported on FTO glass, and it displays reversibly switchable electrochromic behavior in the NIR.
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Electrochromic devices based on binuclear mixed valence compounds adsorbed on nanocrystalline semiconductors.
A series of cyano-bridged binuclear mixed valence complexes of the general formula M-Ru(III)(NH(3))(4)pyCOOH [pyCOOH = isonicotinic acid; M = cis-Ru(bpy)(2)(CN)(2), 1 (bpy = 2,2' bipyridine); trans-Ru(py)(4)(CN)(2), 2 (py = pyridine); [Ru(CN)(6)](4)(-), 3; [Fe(CN)(6)](4)(-), 4] have been prepared and anchored through the carboxylic function to nanocrystalline TiO(2) or SnO(2) electrodes. The complexes display a reversible electrochromic behavior in the range of applied potential from -0.5 to +0.5 V, versus SCE. Tuning of the electronic transitions in the visible and near-infrared spectral regions is achieved through changes of the solvent and of the cyano-bridged metal moiety M.
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