


Molecular Environmental Sciences
Dalton Abdala's webpage

Figure 1. Oryza Officinalis wild rice: the resolution is 2.5 µm.

Figure 2. Oryza Officinalis wild rice: the resolution is 2.5 µm.

nano-FTIR beamline
Infrared spectroscopy (FTIR) is one of the most established techniques for chemical
analysis. The IR spectrum covers the energy levels associated to vibrational and rotational modes of molecules, which are particular spectral signatures of the functional groups of molecules. These natural vibrational modes of molecules allow applying FTIR on the analysis of composition of almost all materials. However, many fundamental properties and functions of materials are described by means of structural-chemical phases in domains or interfaces in the nanometer to few microns scale. In this scenario, techniques able to perform FTIR in sub-micron spatial resolution are highly demanded for developing cutting edge research in new synthetic materials or for the understanding of basic properties of natural materials.
The infrared beamline of the LNLS (IR1) is dedicated to FTIR experiments with
lateral resolution down to few tens of nanometers (nano-FTIR) in the mid-IR range. The
highly intense broadband IR, up to 1000 times more intense than conventional thermal sources, is generated from both bending magnetic and edge radiation, extracted from two consecutives 1.67 T dipoles in the 1.37 GeV storage ring. The extracted IR is then focused and collimated after a set of 5 mirrors, as illustrated in the optics layout of Figure 1.
In order to achieve nanoscale spatial resolution, the IR1 beamline handles the IR
light in the near-field regime. It is well understood that light focusing is ruled by the diffraction limit and that means focal points cannot be smaller than ~λ/2. Therefore in the mid-IR range, microscopy techniques work with a typical pixel size of 4 µm. In the case of the IR1, light is focused towards a metallic tip of an atomic force microscope (AFM). The antenna effect of the elongated metallic AFM tip causes an enhancement of the incident field at the end of the tip, creating an intense evanescent field at the apex of the tip. The result is a new source with a size comparable to the tip apex diameter. The technique is called appertureless-Scanning Near-Field Microscopy (a-SNOM) (Keilmann & Hillenbrand, 2004) and a scheme of the tip-sample with the incident and scattered fields is showed in Figure 2.
The incident and the evanescent waves at the tip apex interact with the sample
surface during AFM tapping-mode topography scans generating two images: one from the mechanical topography and other from the optical interaction of the near-field, as shown in Figure 3. The back-scattered optical signal is lock-in detected in the frequency of the tip in order to separate the near-field from the far-field signal.
Figure 3. Oryza Officinalis wild rice: the resolution is 2.5 µm.

