纳米棒
异质结
拉曼光谱
材料科学
基质(水族馆)
纳米技术
电子转移
光电子学
表面增强拉曼光谱
激光器
拉曼散射
化学
光学
光化学
物理
地质学
海洋学
作者
Songyang Xie,Kun‐Yu Lai,Chenjie Gu,Tao Jiang,L. Zhou,Xiaorui Zheng,Xiang Shen,Jiaguang Han,Jun Zhou
标识
DOI:10.1016/j.mtnano.2022.100179
摘要
Metal-oxide surface-enhanced Raman spectroscopy (SERS) substrates have attracted enormous attentions for trace-level molecule detection, and efficient photo-induced charge transfer is crucial to further enhance the SERS sensitivity. Herein, TiO2@MoOx nanorods are finely prepared to construct the TiO2/MoOx nano-heterojunctions, and then they are implemented as an efficient charge transfer substrate for SERS application. The SERS performance of the substrate is evaluated by using a 532-nm laser as the excitation source and R6G molecules as the Raman reporter. Experimental results show that R6G's Raman signal intensity is gradually improved with the increase of the nano-heterojunction numbers on TiO2@MoOx nanorods. A limit of detection as low as 10−8 M ([email protected] × 10−13 M/cm2) and Raman enhancement factor of 1.445 × 108 ([email protected]−8 M) can be achieved on the most optimal TiO2@MoOx nanorods. Moreover, the mechanism of the SERS enhancement is investigated by analyzing the TiO2 and MoOx band diagrams. It evidences that TiO2@MoOx forms staggered gap heterojunction. Under the laser irradiation, the photo-generate electron-hole pairs are separated in the depletion region and then free electrons move toward the MoOx surface. Thereafter, the electrons are further transferred to the molecules enhancing the SERS performance. Finally, to verify the aforementioned explanation, the surface potential of a single TiO2@MoOx nanorod is measured by Kelvin prober force microscope, it exhibits that the surface potential distribution shifts to a higher level under the light illumination, confirming the accumulation of free electrons on the MoOx surface, and then enhancing charge transfer between the molecules and heterojunctions.
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