论文标题
合金纳米结构的计算设计用于氢的光学传感
Computational Design of Alloy Nanostructures for Optical Sensing of Hydrogen
论文作者
论文摘要
PD纳米合金作为无滞后,可靠的氢传感器具有巨大的潜力。在这里,采用多尺度建模方法来确定使用PD-AU-H系统进行光学氢传感的最佳条件。氢压力的变化转化为氢含量的变化和最终的光谱。在单个粒子水平上,对于氢浓度(即“光学”灵敏度),等离子峰位置的移位在180 nm/c_h的纳米磁直径> 〜100 nm的位置约为180 nm/c_h。对于较小的颗粒,由于第二个峰出现了源自局部表面等离子体和带间跃迁之间的耦合,因此光学灵敏度为负,并且随直径降低而增加。除了跟踪峰位置外,还考虑了固定波长处的灭绝和灭绝的开始。我们仔细地将仿真结果与实验数据进行了比较,并评估了差异的潜在来源。结果始终表明,具有工程组成和/或几何形状无法克服的光敏感性存在上限。虽然合金组成对光学灵敏度的影响有限,但它可以强烈影响H的吸收,从而产生“热力学”灵敏度和检测极限。在这里,它显示了如何通过组成工程来改进后者,甚至通过形成有序相的形成可以在较高的氢部分压力下合成的有序相。
Pd nanoalloys show great potential as hysteresis-free, reliable hydrogen sensors. Here, a multi-scale modeling approach is employed to determine optimal conditions for optical hydrogen sensing using the Pd-Au-H system. Changes in hydrogen pressure translate to changes in hydrogen content and eventually the optical spectrum. At the single particle level, the shift of the plasmon peak position with hydrogen concentration (i.e., the "optical" sensitivity) is approximately constant at 180 nm/c_H for nanodisk diameters >~ 100 nm. For smaller particles, the optical sensitivity is negative and increases with decreasing diameter, due to the emergence of a second peak originating from coupling between a localized surface plasmon and interband transitions. In addition to tracking peak position, the onset of extinction as well as extinction at fixed wavelengths is considered. We carefully compare the simulation results with experimental data and assess the potential sources for discrepancies. Invariably, the results suggest that there is an upper bound for the optical sensitivity that cannot be overcome by engineering composition and/or geometry. While the alloy composition has a limited impact on optical sensitivity, it can strongly affect H uptake and consequently the "thermodynamic" sensitivity and the detection limit. Here, it is shown how the latter can be improved by compositional engineering and even substantially enhanced via the formation of an ordered phase that can be synthesized at higher hydrogen partial pressures.