拉曼光谱
材料科学
激光器
扫描电子显微镜
辐照
激光功率缩放
微秒
纳米结构
分析化学(期刊)
光谱学
纳米颗粒
范德瓦尔斯力
光电子学
纳米技术
光学
化学
分子
物理
有机化学
色谱法
量子力学
核物理学
复合材料
作者
Dmitry Cheshev,Raúl D. Rodriguez,Aleksandar Matković,Alexey Ruban,Jin‐Ju Chen,Evgeniya Sheremet
出处
期刊:ACS omega
[American Chemical Society]
日期:2020-04-24
卷期号:5 (17): 10183-10190
被引量:6
标识
DOI:10.1021/acsomega.0c01079
摘要
We report the high-powered laser modification of the chemical, physical, and structural properties of the two-dimensional (2D) van der Waals material GaSe. Our results show that contrary to expectations and previous reports, GaSe at the periphery of a high-power laser beam does not entirely decompose into Se and Ga2O3. In contrast, we find unexpectedly that the Raman signal from GaSe gets amplified around regions where it was not expected to exist. Atomic force microscopy (AFM), dielectric force microscopy (DFM), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX) results show that laser irradiation induces the formation of nanoparticles. Our analyses demonstrate that, except for a fraction of Ga2Se3, these nanoparticles still belong to the GaSe phase but possess different electrical and optical properties. These changes are evidenced in the increased Raman intensity attributed to the near-resonance conditions with the Raman excitation laser. The elemental analysis of nanoparticles shows that the relative selenium content increased to as much as 70% from a 50:50 value in stoichiometric GaSe. This elemental change is related to the formation of the Ga2Se3 phase identified by Raman spectroscopy at some locations near the edge. Further, we exploit the localized high-power laser processing of GaSe to induce the formation of Ag–GaSe nanostructures by exposure to a solution of AgNO3. The selective reaction of AgNO3 with laser-irradiated GaSe gives rise to composite nanostructures that display photocatalytic activity originally absent in the pristine 2D material. The photocatalytic activity was investigated by the transformation of 4-nitrobenzenethiol to its amino and dimer forms detected in situ by Raman spectroscopy. This work improves the understanding of light–matter interaction in layered systems, offering an approach to the formation of laser-induced composites with added functionality.
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