California NanoSystems Institute, University of California, Los Angeles, Los Angeles, California 90095, United States.
Nano Lett. 2011 Aug 10;11(8):3447-52. doi: 10.1021/nl2019195. Epub 2011 Jul 18.
We apply in situ surface-enhanced Raman spectroscopy (SERS) to probe the reversible photoswitching of azobenzene-functionalized molecules inserted in self-assembled monolayers that serve as controlled nanoscale environments. Nanohole arrays are fabricated in Au thin films to enable SERS measurements associated with excitation of surface plasmons. A series of SERS spectra are recorded for azobenzene upon cycling exposure to UV (365 nm) and blue (450 nm) light. Experimental spectra match theoretical calculations. On the basis of both the simulations and the experimental data analysis, SERS provides quantitative information on the reversible photoswitching of azobenzene in controlled nanoscale environments.
我们应用原位表面增强拉曼光谱(SERS)来探测插入自组装单层中的偶氮苯功能化分子的可逆光致开关,自组装单层可用作控制的纳米级环境。在金薄膜中制造纳米孔阵列,以实现与表面等离子体激元激发相关的 SERS 测量。对在暴露于紫外(365nm)和蓝光(450nm)光之间循环的偶氮苯进行一系列 SERS 光谱记录。实验光谱与理论计算相匹配。基于模拟和实验数据分析,SERS 提供了在控制的纳米级环境中偶氮苯可逆光致开关的定量信息。