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Modified Metal Oxide Nanostructure Deposited Semiconductor Interfaces: Tuning the Lewis Acidity of Reversibly Interacting Sites

机译:改性金属氧化物纳米结构沉积半导体界面:调整可逆相互作用位点的路易斯酸度

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We study the reversible response matrices formed at room temperature as metal oxide nanostructure decorated interfaces are modified through in-situ nitridation. Nanostructured TiO_2, SnO_x, NiO, and Cu_xO (x = 1,2), in order of decreasing Lewis acidity, are deposited to an n-type nanopore coated microporous porous silicon interface to direct a dominant electron transduction process for reversible chemical sensing in the absence of significant chemical bond formation. The in-situ modification of the metal oxides deposited to the interface changes the reversible interaction with the analytes NH_3 and NO. The changes of the responses to the analyte are predictable within the framework of the Inverse Hard/Soft Acid/Base model. The trends are characterized by XPS measurements of the shift in the binding energy from that of the oxides and by infrared spectroscopy. Thus, nitridation significantly changes the response matrix for a given gas and creates a distinct new family of response matrices.
机译:我们研究在室温下形成的可逆响应矩阵,因为通过原位氮化改变了金属氧化物纳米结构装饰界面。纳米结构TiO_2,SNO_X,NIO和CU_XO(X = 1,2)沉积在N型纳米孔涂覆的微孔多孔多孔多孔硅界面上,以引导主要的电子转导过程以进行可逆化学感测没有显着的化学键形成。沉积在界面上的金属氧化物的原位修饰会改变与分析物NH_3和NO的可逆相互作用。对分析物的反应的变化是可预测的逆硬/软酸/基础模型的框架内。趋势的特征在于XPS测量与氧化物的结合能量的换档和红外光谱。因此,氮化显着改变给定气体的响应矩阵,并产生一个不同的新的响应矩阵族。

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