Wang Chih-Feng, Cheng Zhihua, O'Callahan Brian T, Crampton Kevin T, Jones Matthew R, El-Khoury Patrick Z
Physical Sciences Division, Pacific Northwest National Laboratory, P.O. Box 999, Richland, Washington 99352, United States.
Department of Chemistry, Department of Materials Science & Nanoengineering, Rice University, 6100 Main Street, Houston, Texas 77005, United States.
J Phys Chem Lett. 2020 Apr 2;11(7):2464-2469. doi: 10.1021/acs.jpclett.0c00559. Epub 2020 Mar 13.
We record nanoscale chemical images of thiobenzonitrile (TBN)-functionalized plasmonic gold nanocubes via tip-enhanced Raman spectroscopy (TERS). The spatially averaged optical response is dominated by conventional (dipolar) TERS scattering from TBN but also contains weaker spectral signatures in the 1225-1500 cm region. The weak optical signatures dominate several of the recorded single-pixel TERS spectra. We can uniquely assign these Raman-forbidden transitions to multipolar Raman scattering, which implicates spatially varying enhanced electric field gradients at plasmonic tip-sample nanojunctions. Specifically, we can assign observations of tip-enhanced electric dipole-magnetic dipole as well as electric dipole-electric quadrupole driven transitions. Multipolar Raman scattering and local optical field gradients both need to be understood and accounted for in the interpretation of TERS spectral images, particularly in ongoing quests aimed at chemical reaction mapping via TERS.
我们通过针尖增强拉曼光谱(TERS)记录了硫代苯甲腈(TBN)功能化的等离子体金纳米立方体的纳米级化学图像。空间平均光学响应主要由TBN的传统(偶极)TERS散射主导,但在1225 - 1500厘米区域也包含较弱的光谱特征。这些微弱的光学特征在几个记录的单像素TERS光谱中占主导地位。我们可以将这些拉曼禁戒跃迁唯一地归因于多极拉曼散射,这意味着在等离子体针尖 - 样品纳米结处存在空间变化的增强电场梯度。具体而言,我们可以确定观察到的针尖增强电偶极 - 磁偶极以及电偶极 - 电四极驱动的跃迁。在解释TERS光谱图像时,特别是在通过TERS进行化学反应映射的持续探索中,多极拉曼散射和局部光场梯度都需要被理解和考虑。