Browsing by Author "Guan, B"

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    Depth-resolved chemical modification of porous silicon by wavelength-tuned irradiation
    (American Chemical Society, 2012-11-06) Guan, B; Ciampi, S; Luais, E; James, M; Reece, PJ; Gooding, JJ
    The ability to impart discrete surface chemistry to the inside and outside of mesoporous silicon is of great importance for a range of biomedical applications, from selective (bio)sensing to tissue-specific drug delivery. Here we present a generic strategy toward achieving depth-resolved functionalization of the external and internal porous surfaces by a simple change in the wavelength of the light being used to promote surface chemical reactions. UV-assisted hydrosilylation, limited by the penetration depth of UV light, is used to decorate the outside of the mesoporous structure with carboxylic acid molecules, and white light illumination triggers the attachment of dialkyne molecules to the inner porous matrix. © 2012, American Chemical Society.
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    The effect of molybdenum on clustering and precipitation behaviour of strip-cast steels containing niobium
    (Elsevier B. V., 2019-12) Jiang, L; Marceau, RKW; Guan, B; Dorin, T; Wood, K; Hodgson, PD; Stanford, N
    Two high-strength low-alloy (HSLA) steels containing Nb-carbonitrides were produced, one contained Mo and the other was Mo-free. The alloys were produced by simulated direct strip casting, and were fully bainitic in the as-cast condition. Isothermal ageing treatments were carried out to precipitate harden the alloy, and the strength was measured using a shear punch test. The dislocation density was measured with X-ray diffraction (XRD), and was found to be larger in the alloy containing Mo in all ageing conditions. Atom probe tomography (APT) showed the presence of solute clusters in the as-cast condition, and the addition of Mo increased both size and volume fraction of these clusters. The solute clusters provided significant strengthening increments of up to 112 MPa, and cluster strengthening was larger in the Mo-containing alloy. Precipitation of Nb-carbonitrides was observed after longer ageing times, which were refined by the addition of Mo. This was attributed to the higher dislocation density that increased the number of nucleation sites. Precipitate chemistry was similar for both alloys, and contrary to some literature reports, minimal Mo was observed to segregate to the precipitates. A thermodynamic rationale is presented which describes the reasons that Mo segregates to the Nb-carbide in some alloys but not in others, despite the alloy chemistries being relatively similar. © 2019 Acta Materialia Inc.
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    Oxidative acetylenic coupling reactions as a surface chemistry tool
    (2011-09-14) Ciampi, S; James, M; Darwish, N; Luais, E; Guan, B; Harper, JB; Gooding, JJ
    A novel method to prepare redox monolayers on silicon electrodes has been developed that employs CuI-catalyzed oxidative acetylenic coupling reactions for molecular electronic type applications. As the first case study, ethynylferrocene was covalently immobilized onto an acetylene-terminated monolayer on a Si(100) surface to give a 1,3-diyne (C[triple bond, length as m-dash]C-C[triple bond, length as m-dash]C-) linked redox assembly. The derivatization process requires no protection/de-protection steps, nor activation procedures. The effect of the conjugated diyne linkage on the rate of electron transfer between tethered ferrocenyl units and the silicon electrode is benchmarked against well-established "click" products (i.e. 1,2,3-triazole linkage). The surfaces, after each step, are characterized thoroughly using X-ray reflectivity (XRR), X-ray photoelectron spectroscopy (XPS), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The coupling chemistry provides a useful strategy for functionalizing silicon surfaces and contributes to an expanding repertoire of wet chemistry routes for the functionalization of solid substrates.© 2011, Royal Society of Chemistry