Search arXivSearch

arXiv · 1911.12097

Spatial Resolution, Sensitivity and Surface Selectivity in Resonant Mode Photothermal Induced Resonance Spectroscopy

Abstract

Photothermal-Induced Resonance (PTIR) is increasingly used in the measurement of infrared absorption spectra of sub-micrometer objects. The technique measures IR absorption spectra by relying on the photothermal effect induced by a rapid pulse of light and the excitation of the resonance spectrum of an AFM cantilever in contact with the sample. In this work we assess the spatial resolution and depth response of PTIR in resonant mode while systematically varying the pulsing frequency of the excitation laser and the cantilever resonance. The spatial resolution shows a shallow linear dependence on the inverse of the pulse frequency, which rules out tip size as a limiting factor for resolution in the frequency range under investigation. Measured resolution values are also one order of magnitude lower than in the thermal diffusion limit, excluding thermal wave propagation as a limiting factor. We also show that the pulsing frequency of the laser and choice of cantilever resonance affect the intensity of the signal and the surface selectivity in PTIR images, with higher frequencies providing increased surface selectivity. The results confirm a difference in signal generation between resonant PTIR and other photothermal techniques and indicate that photothermal induced heating and expansion cannot fully account for observed intensity and resolution.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Luca Quaroni. 2019-11-27. Spatial Resolution, Sensitivity and Surface Selectivity in Resonant Mode Photothermal Induced Resonance Spectroscopy. https://arxiv.org/abs/1911.12097

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Intrinsic Matching Frustration in Fluctuating Finite Systems

We formulate intrinsic matching frustration (IMF), a fluctuation-induced, kinetics-independent reduction in the mean capacity permitted by a prescribed matching rule. For complementary one-to-one matching, the instantaneous capacity is set by the minority population, so fluctuations produce a nonzero mean deficit even when the two populations are balanced on average. At finite size, this deficit depends on the full distribution of the population difference and is determined by its variance alone only in the Gaussian limit. Compartmentalization hides matching capacity by preventing cancellation between local imbalances of opposite sign. Fusion releases this hidden capacity monotonically under coarse graining, producing a measurable recovery of product yield following local reaction to completion.

physics.chem-ph

Phonon chirality as an additive control of CISS: a symmetry-protected law

Chirality-induced spin selectivity (CISS) is usually associated with molecular handedness. The possible contribution of chiral phonons is less established. We study a helical tight-binding model in which local phonon angular momentum modulates spin-dependent nearest-neighbor hopping. Fewest-switches surface hopping calculations give the transmitted spin polarization $\mathrm{SP}=aC+b\mathrm{PH}$. Here $C$ is the molecular chirality and $\mathrm{PH}$ is the phonon chirality. A mirror symmetry reverses $C$, $\mathrm{PH}$, and $\mathrm{SP}$ simultaneously. This symmetry excludes both a chirality-independent offset and a $C\cdot\mathrm{PH}$ term. The phonon contribution can therefore enhance, cancel, or reverse the molecular CISS signal.

physics.chem-ph

A fast physics-based matrix model for the impedance of a PEM fuel cell: Incorporating functionally graded catalyst layer and channel impedances

We extend a recent physics-based matrix model for calculating PEM fuel cell impedance (doi:10.1149/2754-2734/ad6ce8) to cases of low air flow stoichiometry and functionally graded cathode catalyst layers (CCLs). We demonstrate that the matrix model produces accurate spectra and is almost three orders of magnitude faster than a model based on the standard boundary-value problem solver. The physics-based matrix model can compete with equivalent circuit models for fitting experimental EIS spectra, particularly those measured from cells with functionally graded CCL.

physics.chem-ph