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利用超高真空针尖增强 Raman 光谱技术对动态分子相界的纳米尺度化学成像。

Nanoscale Chemical Imaging of a Dynamic Molecular Phase Boundary with Ultrahigh Vacuum Tip-Enhanced Raman Spectroscopy.

机构信息

Department of Chemistry, University of Illinois at Chicago , Chicago, Illinois 60607, United States.

出版信息

Nano Lett. 2016 Jun 8;16(6):3898-904. doi: 10.1021/acs.nanolett.6b01405. Epub 2016 May 19.

Abstract

Nanoscale chemical imaging of a dynamic molecular phase boundary has broad implications for a range of problems in catalysis, surface science, and molecular electronics. While scanning probe microscopy (SPM) is commonly used to study molecular phase boundaries, its information content can be severely compromised by surface diffusion, irregular packing, or three-dimensional adsorbate geometry. Here, we demonstrate the simultaneous chemical and structural analysis of N-N'-bis(2,6-diisopropylphenyl)-1,7-(4'-t-butylphenoxy)perylene-3,4:9,10-bis(dicarboximide) (PPDI) molecules by UHV tip-enhanced Raman spectroscopy. Both condensed and diffusing domains of PPDI coexist on Ag(100) at room temperature. Through comparison with time-dependent density functional theory simulations, we unravel the orientation of PPDI molecules at the dynamic molecular domain boundary with unprecedented ∼4 nm spatial resolution.

摘要

纳米尺度化学成像的动态分子相界在催化、表面科学和分子电子学等一系列问题上具有广泛的意义。虽然扫描探针显微镜 (SPM) 常用于研究分子相界,但表面扩散、不规则堆积或三维吸附物几何形状会严重影响其信息含量。在这里,我们通过超真空尖端增强拉曼光谱法证明了 N-N'-双 (2,6-二异丙基苯基) -1,7-(4'-叔丁基苯氧基)苝-3,4:9,10-双 (二羧酸二酰亚胺) (PPDI) 分子的化学和结构同时分析。在室温下,PPDI 在 Ag(100) 上共存于凝聚和扩散区域。通过与时间相关的密度泛函理论模拟进行比较,我们以空前的约 4nm 空间分辨率揭示了动态分子畴边界处 PPDI 分子的取向。

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