Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, 20742, USA.
Maryland NanoCenter, University of Maryland, College Park, MD, 20742, USA.
Adv Mater. 2020 Apr;32(14):e1906517. doi: 10.1002/adma.201906517. Epub 2020 Feb 20.
Organic color-centers (OCCs) have emerged as promising single-photon emitters for solid-state quantum technologies, chemically specific sensing, and near-infrared bioimaging. However, these quantum light sources are currently synthesized in bulk solution, lacking the spatial control required for on-chip integration. The ability to pattern OCCs on solid substrates with high spatial precision and molecularly defined structure is essential to interface electronics and advance their quantum applications. Herein, a lithographic generation of OCCs on solid-state semiconducting single-walled carbon nanotube films at spatially defined locations is presented. By using light-driven diazoether chemistry, it is possible to directly pattern p-nitroaryl OCCs, which demonstrate chemically specific spectral signatures at programmed positions as confirmed by Raman mapping and hyperspectral photoluminescence imaging. This light-driven technique enables the fabrication of OCC arrays on solid films that fluoresce in the shortwave infrared and presents an important step toward the direct writing of quantum emitters and other functionalities at the molecular level.
有机色心 (OCC) 已成为固态量子技术、化学特异性传感和近红外生物成像中很有前途的单光子发射器。然而,这些量子光源目前是在 bulk solution 中合成的,缺乏用于片上集成的空间控制。在固体衬底上以高空间精度和分子定义结构对 OCC 进行图案化的能力对于接口电子学和推进它们的量子应用至关重要。在此,提出了在空间限定位置的固态半导体单壁碳纳米管薄膜上通过光刻生成 OCC。通过使用光驱动的重氮醚化学,可以直接对 p-硝基芳基 OCC 进行图案化,通过拉曼映射和高光谱荧光成像证实了在编程位置具有化学特异性光谱特征。这种光驱动技术能够在固体薄膜上制造在短波红外中发射荧光的 OCC 阵列,这是朝着在分子水平上直接写入量子发射器和其他功能迈出的重要一步。