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Effect of Solution Conditions on the Properties of Sol–Gel Derived Potassium Sodium Niobate Thin Films on Platinized Sapphire Substrates

机译:固溶条件对镀铂蓝宝石衬底上溶胶-凝胶衍生铌酸钾钠薄膜性能的影响

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摘要

If piezoelectric micro-devices based on K Na NbO (KNN) thin films are to achieve commercialization, it is critical to optimize the films’ performance using low-cost scalable processing conditions. Here, sol–gel derived KNN thin films are deposited using 0.2 and 0.4 M precursor solutions with 5% solely potassium excess and 20% alkali (both potassium and sodium) excess on platinized sapphire substrates with reduced thermal expansion mismatch in relation to KNN. Being then rapid thermal annealed at 750 °C for 5 min, the films revealed an identical thickness of ~340 nm but different properties. An average grain size of ~100 nm and nearly stoichiometric KNN films are obtained when using 5% potassium excess solution, while 20% alkali excess solutions give the grain size of 500–600 nm and (Na + K)/Nb ratio of 1.07–1.08 in the prepared films. Moreover, the 5% potassium excess solution films have a perovskite structure without clear preferential orientation, whereas a (100) texture appears for 20% alkali excess solutions, being particularly strong for the 0.4 M solution concentration. As a result of the grain size and (100) texturing competition, the highest room-temperature dielectric permittivity and lowest dissipation factor measured in the parallel-plate-capacitor geometry were obtained for KNN films using 0.2 M precursor solutions with 20% alkali excess. These films were also shown to possess more quadratic-like and less coercive local piezoelectric loops, compared to those from 5% potassium excess solution. Furthermore, KNN films with large (100)-textured grains prepared from 0.4 M precursor solution with 20% alkali excess were found to possess superior local piezoresponse attributed to multiscale domain microstructures.
机译:如果要实现基于K Na NbO(KNN)薄膜的压电微器件的商业化,使用低成本可扩展的加工条件来优化薄膜的性能至关重要。在这里,溶胶-凝胶衍生的KNN薄膜使用0.2和0.4 M的前体溶液沉积,其中仅5%的钾肥和20%的碱金属(钾和钠)分别在镀蓝宝石衬底上沉积,相对于KNN而言,热膨胀失配性降低。然后将其在750°C的温度下快速热退火5分钟,显示出约340 nm的相同厚度,但性能不同。当使用5%的过量钾溶液时,平均晶粒尺寸为〜100 nm,接近化学计量的KNN膜,而20%的碱性过量溶液的晶粒尺寸为500–600 nm,(Na + K)/ Nb比为1.07–在制备的膜中为1.08。此外,5%钾过量溶液薄膜具有钙钛矿结构,没有明确的优先取向,而对于20%碱过量溶液则呈现(100)织构,对于0.4M溶液浓度特别强。由于晶粒尺寸和(100)织构竞争,使用0.2M前体溶液和20%碱过量的KNN薄膜,在平行板电容器几何结构中测得的最高室温介电常数和最低损耗因子。与来自5%过量钾溶液的薄膜相比,这些薄膜还显示出具有更多的二次方形和更小的矫顽局部压电环。此外,发现由具有20%碱过量的0.4 M前体溶液制备的具有大(100)织构化晶粒的KNN膜具有归因于多尺度域微结构的优越的局部压电响应。

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