Zhang Wei, Ai Bin, Gu Panpan, Guan Yuduo, Wang Zengyao, Xiao Zifan, Zhang Gang
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun 130012, P.R. China.
School of Microelectronics and Communication Engineering, Chongqing Key Laboratory of Bio-perception & Intelligent Information Processing, Chongqing University, Chongqing 400044, P.R. China.
ACS Nano. 2021 Nov 23;15(11):17657-17667. doi: 10.1021/acsnano.1c05437. Epub 2021 Nov 4.
Sub-10 nm nanogaps are enantioselectively fabricated between two nanocrescents based on nanoskiving and show tailored circular dichroism (CD) activity. The mirror symmetry of the nanostructure is broken by subsequent deposition with different azimuthal angles. Strong plasmonic coupling is excited in the gaps and at the tips, leading to the CD activity. The dissymmetry -factor of the chiral nanogaps with 5 nm gap-width is -0.055, which is 2.5 times stronger than that of the 10 nm gap-width. Moreover, the surface-enhanced Raman scattering (SERS) performance of l/d-cysteine absorbed on chiral nanogaps manifests as the emergence of enantiospecific Raman peaks and the appearance of distinct changes in SERS intensities, which affirms that chiral nanogaps can recognize specific cysteine enantiomers standard Raman spectroscopy in the absence of circularly polarized light source and a chiral label molecule. The sub-10 nm chiral nanogaps with tailored chiroptical responses show great potential in a class of chiral applications, such as chiral sensing, polarization converters, label-free chiral recognition, and asymmetric catalysis.
基于纳米削薄技术,在两个纳米月牙之间对小于10纳米的纳米间隙进行对映选择性制备,并展示出定制的圆二色性(CD)活性。通过随后以不同方位角进行沉积,纳米结构的镜像对称性被打破。在间隙和尖端激发了强烈的等离子体耦合,从而导致了CD活性。具有5纳米间隙宽度的手性纳米间隙的不对称因子为-0.055,比10纳米间隙宽度的不对称因子强2.5倍。此外,吸附在手性纳米间隙上的l/d-半胱氨酸的表面增强拉曼散射(SERS)性能表现为对映体特异性拉曼峰的出现以及SERS强度的明显变化,这证实了手性纳米间隙在没有圆偏振光源和手性标记分子的情况下能够识别特定的半胱氨酸对映体 标准拉曼光谱。具有定制手性光学响应的小于10纳米的手性纳米间隙在一类手性应用中显示出巨大潜力,如手性传感、偏振转换器、无标记手性识别和不对称催化。