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Silver-nanoparticle dispersion from the consolidation of Ag-attached silica colloid

机译:附着银的二氧化硅胶体固结产生的银-纳米颗粒分散体

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摘要

Silver nanoparticles dispersed in a silica matrix were made by the consolidation of a Ag-attached silica colloid, which was synthesized via the electrolysis of a pure Ag electrode, the reduction of Ag~+ ions by H_2, and the nucleation and growth of Ag particles on the silica nanoparticles in water. This simple process produced Ag/silica nanocomposites with a high concentration and narrow size distribution of nanoparticles, which was confirmed by transmission electron microscopy and x-ray diffraction. As estimated by Raman and photoluminescence measurements, the quantity of broken oxygen bonds was increased with increasing Ag concentration due to the intervention of Ag ions as structural modifiers in the silica network structure. Ag ions in the matrix are probably a residue of the Ag~+ ions that could not be reduced by H_2 during the electrolysis/reduction reaction. The optical-absorption spectra and the HCl-soaking test suggested that a chemical-interface damping effect, which was caused by electron transfer from the metal particles to the oxide matrix, dominates the optical-absorption properties in this system.
机译:通过固结Ag的二氧化硅胶体的固结来制备分散在二氧化硅基质中的银纳米颗粒,该固结是通过纯Ag电极的电解,H_2还原Ag〜+离子以及Ag颗粒的成核和生长而合成的在水中的二氧化硅纳米粒子上。这个简单的过程生产出具有高浓度和窄尺寸分布的纳米颗粒的Ag /二氧化硅纳米复合材料,这已通过透射电子显微镜和X射线衍射得到了证实。如通过拉曼和光致发光测量所估计的,由于Ag离子作为二氧化硅网络结构的结构改性剂的干预,断裂的氧键的数量随着Ag浓度的增加而增加。基质中的Ag离子可能是Ag〜+离子的残留物,在电解/还原反应过程中无法被H_2还原。光吸收光谱和HCl浸泡测试表明,由电子从金属颗粒转移到氧化物基质引起的化学界面阻尼效应主导了该系统的光吸收性能。

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