Moram Sree Satya Bharati, Byram Chandu, Soma Venugopal Rao
Advanced Centre for Research in High Energy Materials (ACRHEM), DRDO Industry Academia - Centre of Excellence (DIA-COE), University of Hyderabad, Prof. C. R. Rao Road, Hyderabad 500046, Telangana, India.
Department of Physics, Indian Institute of Technology Hyderabad, Kandi 502285, Telangana, India.
Beilstein J Nanotechnol. 2024 Aug 19;15:1054-1069. doi: 10.3762/bjnano.15.86. eCollection 2024.
The present study investigates the effects of input wavelength (1064, 532, and 355 nm) and surrounding liquid environment (distilled water and aqueous NaCl solution) on the picosecond laser ablation on silver (Ag), gold (Au), and Ag/Au alloy targets. The efficacy of the laser ablation technique was meticulously evaluated by analyzing the ablation rates, surface plasmon resonance peak positions, and particle size distributions of the obtained colloids. The nanoparticles (NPs) were characterized using the techniques of UV-visible absorption, transmission electron microscopy, and energy-dispersive X-ray spectroscopy. Furthermore, NPs of various sizes ranging from 6 to 35 nm were loaded onto a filter paper by a simple and effective drop-casting approach to achieve flexible surface-enhanced Raman spectroscopy (SERS) substrates/sensors. These substrates were tested using a simple, portable Raman device to identify various hazardous chemicals (malachite green, methyl salicylate, and thiram). The stability of the substrates was also systematically investigated by determining the decay percentages in the SERS signals over 60 days. The optimized SERS substrate was subsequently employed to detect chemical warfare agent (CWA) simulants such as methyl salicylate (a CWA simulant for sulfur mustard) and dimethyl methyl phosphonate (has some structural similarities to the G-series nerve agents) at different laser excitations (325, 532, and 633 nm). A notably higher SERS efficiency for CWA simulants was observed at a 325 nm Raman excitation. Our findings reveal that a higher ablation yield was observed at IR irradiation than those obtained at the other wavelengths. A size decrease of the NPs was noticed by changing the liquid environment to an electrolyte. These findings have significant implications for developing more efficient and stable SERS substrates for chemical detection applications.
本研究调查了输入波长(1064、532和355纳米)以及周围液体环境(蒸馏水和氯化钠水溶液)对银(Ag)、金(Au)和Ag/Au合金靶材的皮秒激光烧蚀的影响。通过分析烧蚀速率、表面等离子体共振峰位置以及所得胶体的粒径分布,对激光烧蚀技术的效果进行了细致评估。使用紫外可见吸收、透射电子显微镜和能量色散X射线光谱技术对纳米颗粒(NPs)进行了表征。此外,通过一种简单有效的滴铸方法,将6至35纳米范围内的各种尺寸的纳米颗粒加载到滤纸上,以制备柔性表面增强拉曼光谱(SERS)基底/传感器。使用一种简单的便携式拉曼装置对这些基底进行测试,以识别各种危险化学品(孔雀石绿、水杨酸甲酯和福美双)。还通过测定60天内SERS信号的衰减百分比,系统地研究了基底的稳定性。随后,将优化后的SERS基底用于在不同激光激发(325、532和633纳米)下检测化学战剂(CWA)模拟物,如水杨酸甲酯(硫芥的CWA模拟物)和甲基膦酸二甲酯(与G系列神经毒剂有一些结构相似性)。在325纳米拉曼激发下,观察到CWA模拟物的SERS效率显著更高。我们的研究结果表明,与其他波长相比,红外照射下的烧蚀产率更高。通过将液体环境改为电解质,发现纳米颗粒的尺寸减小。这些发现对于开发用于化学检测应用的更高效、稳定的SERS基底具有重要意义。