Xie Kai-Xin, Liu Qian, Jia Shu-Shu, Xiao Xiu-Xian
Department of Chemistry, Taiyuan Normal University, Jin Zhong, 030619, PR China.
Laboratory of Pharmacy and Chemistry, Lab Teaching & Management Center, Chongqing Medical University, Chongqing, 400016, PR China.
Anal Chim Acta. 2021 Feb 1;1144:96-101. doi: 10.1016/j.aca.2020.12.008. Epub 2020 Dec 9.
We have observed the enhanced surface plasmon-coupled emission (SPCE) by introducing a hollow plasmonic structure. By assembling gold nanoshells (GNSs) on a gold substrate via electrostatic adsorption and subsequently applying a fluorophore layer (approximately 30 nm) by spin-coating, SPCE fluorescence signals exhibited 30- and 110-fold enhancements compared to those of normal SPCE and free space emission, respectively. This enhancement was mainly induced by the novel "hot-spot" plasmonic structure that emerged between the GNS and gold substrate, the intense electromagnetic field of GNSs, and the strong coupling interactions between fluorescence and surface plasmons. After optimizing the conditions, we demonstrated that this GNS-enhanced SPCE system was suitable for biomolecule detection because of the scale match between the optimal fluorophore thickness and the biomolecule size, and thus was designed as an immunosensor to verify the feasibility of this system. Our strategy of combining GNSs and SPCE to enhance the fluorescence signal created a new fluorescence system based on a hollow plasmonic structure and provided a simple way to improve the detection sensitivity in fluorescence-based sensing and imaging platforms.
我们通过引入中空等离子体结构观察到了增强的表面等离子体耦合发射(SPCE)。通过静电吸附将金纳米壳(GNSs)组装在金基底上,随后通过旋涂施加一层荧光团层(约30 nm),与正常SPCE和自由空间发射相比,SPCE荧光信号分别增强了30倍和110倍。这种增强主要是由GNS与金基底之间出现的新型“热点”等离子体结构、GNSs的强电磁场以及荧光与表面等离子体之间的强耦合相互作用引起的。优化条件后,我们证明这种GNS增强的SPCE系统适用于生物分子检测,因为最佳荧光团厚度与生物分子大小之间存在尺度匹配,因此将其设计为免疫传感器以验证该系统的可行性。我们将GNSs与SPCE相结合以增强荧光信号的策略创建了一种基于中空等离子体结构的新型荧光系统,并为提高基于荧光的传感和成像平台的检测灵敏度提供了一种简单方法。