Powder Technology Laboratory, Materials Science and Engineering Department, EPFL, CH-1015, Lausanne, Switzerland.
Nanoscale. 2010 Nov;2(11):2470-7. doi: 10.1039/c0nr00420k. Epub 2010 Oct 11.
Precipitated oxalates are often nanostructured and can be used as precursors for nanostructured oxides for different applications. The modification of the particle shape and nanostructures of both copper and cobalt oxalates has been demonstrated using polymeric additives or complexing counter-ions. In the case of cobalt oxalate the characteristic elongated rod particle shape (axial ratio of 10) can be modified by using polymethymethacrylate (PMMA) to produce particles with lower axial ratios of 2, through cubes all the way to platelets (axial ratio 0.2). The PMMA inhibits the growth of the particles along the [101] direction more and more strongly as the concentration of the polymer increases. The crystallite size from XRD line broadening is not modified by the PMMA indicating that the PMMA does not influence the nucleation and growth but modifies the aggregation kinetics. Copper oxalates precipitated in the presence of different cellulose derived polymers with different molecular weights and functional groups (methyl and propyl) showed sensitivity to both molecular weight and functional group. Higher molecular weights did not influence the copper oxalate particle shape, whereas methyl cellulose gave elongated particles and propyl celluloses gave platelet like particles. Copper oxalate precipitated in the presence of acetate counter ions gave platelets with an axial ratio of 0.15 compared to the cushion-like morphology (axial ratio 0.5). The primary crystallites were more elongated along the [001] direction in the presence of acetate, modifying the proportion of the hydrophobic and hydrophilic surfaces and hence influencing the aggregation kinetics and particle shape. The copper and cobalt oxalate particle formation seems to be dominated by the primary particle aggregation with the different additives interacting specifically with different crystallographic faces of the primary particles. By tuning this interaction particles with different shapes and substructures can be formed.
沉淀的草酸盐通常是纳米结构的,可作为不同应用的纳米结构氧化物的前体。已经证明,通过使用聚合物添加剂或络合抗衡离子,可以对铜和钴草酸盐的颗粒形状和纳米结构进行修饰。在钴草酸盐的情况下,通过使用聚甲基丙烯酸甲酯(PMMA),可以将特征性的长棒状颗粒形状(轴向比为 10)修饰为具有较低轴向比的颗粒,从 2 到立方体形,一直到板状(轴向比为 0.2)。随着聚合物浓度的增加,PMMA 越来越强烈地抑制颗粒沿着[101]方向的生长。PMMA 不会影响成核和生长,但会改变聚集动力学,这一点可以从 XRD 线宽的晶粒尺寸看出。在 presence of 不同纤维素衍生聚合物 presence of 不同分子量和官能团(甲基和丙基)的铜草酸盐沉淀对分子量和官能团都有敏感性。较高的分子量不会影响铜草酸盐的颗粒形状,而甲基纤维素则给出了长形颗粒,而丙基纤维素则给出了板状颗粒。在 presence of 醋酸盐抗衡离子的情况下沉淀的铜草酸盐给出了具有 0.15 轴向比的板状颗粒,而在 presence of 醋酸盐的情况下,其形态为垫状(轴向比为 0.5)。在 presence of 醋酸盐的情况下,初级晶粒更沿着[001]方向拉长,改变了疏水性和亲水性表面的比例,从而影响了聚集动力学和颗粒形状。铜和钴草酸盐的颗粒形成似乎主要是由初级颗粒的聚集所控制,不同的添加剂与初级颗粒的不同晶面特异性相互作用。通过调整这种相互作用,可以形成具有不同形状和亚结构的颗粒。