Univ. Grenoble Alpes, CEA, LETI, 38000, Grenoble, France.
Centre for Nano Science and Engineering, Indian Institute of Science, Bangalore, 560012, India.
Nat Commun. 2018 Aug 16;9(1):3283. doi: 10.1038/s41467-018-05783-4.
One of the main challenges to overcome to perform nanomechanical mass spectrometry analysis in a practical time frame stems from the size mismatch between the analyte beam and the small nanomechanical detector area. We report here the demonstration of mass spectrometry with arrays of 20 multiplexed nanomechanical resonators; each resonator is designed with a distinct resonance frequency which becomes its individual address. Mass spectra of metallic aggregates in the MDa range are acquired with more than one order of magnitude improvement in analysis time compared to individual resonators. A 20 NEMS array is probed in 150 ms with the same mass limit of detection as a single resonator. Spectra acquired with a conventional time-of-flight mass spectrometer in the same system show excellent agreement. We also demonstrate how mass spectrometry imaging at the single-particle level becomes possible by mapping a 4-cm-particle beam in the MDa range and above.
在实际时间框架内进行纳米机械质谱分析的主要挑战之一源于分析物束与小的纳米机械探测器区域之间的尺寸不匹配。我们在这里报告了使用 20 个复用纳米机械谐振器阵列进行质谱分析的演示;每个谐振器都设计有独特的共振频率,成为其单独的地址。与单个谐振器相比,在分析时间上提高了一个数量级,从而获得了 MDa 范围内金属聚集体的质谱。在 150 毫秒内探测 20 个 NEMS 阵列,其检测限与单个谐振器相同。在同一系统中使用传统的飞行时间质谱仪获得的光谱具有极好的一致性。我们还展示了如何通过对 MDa 范围内及以上的 4 厘米颗粒束进行成像,实现单颗粒水平的质谱成像。