Rani Renu, Yoshimura Anthony, Das Shreeja, Sahoo Mihir Ranjan, Kundu Anirban, Sahu Kisor K, Meunier Vincent, Nayak Saroj K, Koratkar Nikhil, Hazra Kiran Shankar
Institute of Nano Science and Technology, Phase-10, Mohali, Punjab 160062, India.
Department of Physics, Applied Physics, and Astronomy, Rensselaer Polytechnic Institute, Troy, New York 12180, United States.
ACS Nano. 2020 May 26;14(5):6258-6268. doi: 10.1021/acsnano.0c02418. Epub 2020 Apr 29.
Hotspot engineering has the potential to transform the field of surface-enhanced Raman spectroscopy (SERS) by enabling ultrasensitive and reproducible detection of analytes. However, the ability to controllably generate SERS hotspots, with desired location and geometry, over large-area substrates, has remained elusive. In this study, we sculpt artificial edges in monolayer molybdenum disulfide (MoS) by low-power focused laser-cutting. We find that when gold nanoparticles (AuNPs) are deposited on MoS by drop-casting, the AuNPs tend to accumulate predominantly along the artificial edges. First-principles density functional theory (DFT) calculations indicate strong binding of AuNPs with the artificial edges due to dangling bonds that are ubiquitous on the unpassivated (laser-cut) edges. The dense accumulation of AuNPs along the artificial edges intensifies plasmonic effects in these regions, creating hotspots exclusively along the artificial edges. DFT further indicates that adsorption of AuNPs along the artificial edges prompts a transition from semiconducting to metallic behavior, which can further intensify the plasmonic effect along the artificial edges. These effects are observed exclusively for the sculpted (, cut) edges and not observed for the MoS surface (away from the cut edges) or along the natural (passivated) edges of the MoS sheet. To demonstrate the practical utility of this concept, we use our substrate to detect Rhodamine B (RhB) with a large SERS enhancement (∼10) at the hotspots for RhB concentrations as low as ∼10 M. The single-step laser-etching process reported here can be used to controllably generate arrays of SERS hotspots. As such, this concept offers several advantages over previously reported SERS substrates that rely on electrochemical deposition, e-beam lithography, nanoimprinting, or photolithography. Whereas we have focused our study on MoS, this concept could, in principle, be extended to a variety of 2D material platforms.
热点工程有潜力通过实现对分析物的超灵敏和可重复检测来改变表面增强拉曼光谱(SERS)领域。然而,在大面积基板上可控地生成具有所需位置和几何形状的SERS热点的能力仍然难以捉摸。在本研究中,我们通过低功率聚焦激光切割在单层二硫化钼(MoS)中雕刻人工边缘。我们发现,当通过滴铸法将金纳米颗粒(AuNP)沉积在MoS上时,AuNP倾向于主要沿着人工边缘聚集。第一性原理密度泛函理论(DFT)计算表明,由于在未钝化(激光切割)边缘普遍存在的悬空键,AuNP与人工边缘有很强的结合力。AuNP沿着人工边缘的密集聚集增强了这些区域的等离子体效应,仅在人工边缘处产生热点。DFT进一步表明,AuNP沿着人工边缘的吸附促使从半导体行为向金属行为转变,这可以进一步增强沿着人工边缘的等离子体效应。这些效应仅在雕刻(切割)边缘观察到,而在MoS表面(远离切割边缘)或沿着MoS片的自然(钝化)边缘未观察到。为了证明这一概念的实际应用,我们使用我们的基板在热点处检测罗丹明B(RhB),对于低至10 M的RhB浓度,具有大的SERS增强(10)。本文报道的单步激光蚀刻工艺可用于可控地生成SERS热点阵列。因此,与先前报道的依赖电化学沉积、电子束光刻、纳米压印或光刻的SERS基板相比,这一概念具有几个优点。虽然我们将研究重点放在了MoS上,但这一概念原则上可以扩展到各种二维材料平台。