Phal Yamuna, Pfister Luke, Carney P Scott, Bhargava Rohit
Department of Electrical and Computer Engineering, University of Illinois at Urbana - Champaign, Urbana, Illinois 61801, United States; Beckman Institute for Advanced Science and Technology, Urbana, Illinois 61801, United States.
Dynamic Imaging & Radiography Group, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States.
J Phys Chem C Nanomater Interfaces. 2022 Jun 16;126(23):9777-9783. doi: 10.1021/acs.jpcc.2c00740. Epub 2022 May 31.
Chemical imaging combines the spatial specificity of optical microscopy with the spectral selectivity of vibrational spectroscopy. Mid-infrared (IR) absorption imaging instruments are now able to capture high-quality spectra with microscopic spatial detail, but the limits of their ability to resolve spatial and spectral objects remain less understood. In particular, the sensitivity of measurements to chemical and spatial changes and rules for optical design have been presented, but the influence of spectral information on spatial sensitivity is as yet relatively unexplored. We report an information theory-based approach to quantify the spatial localization capability of spectral data in chemical imaging. We explicitly consider the joint effects of the signal-to-noise ratio and spectral separation that have significance in experimental settings to derive resolution limits in IR spectroscopic imaging.
化学成像将光学显微镜的空间特异性与振动光谱的光谱选择性结合起来。中红外(IR)吸收成像仪器现在能够捕获具有微观空间细节的高质量光谱,但它们分辨空间和光谱对象的能力极限仍不太为人所理解。特别是,已经提出了测量对化学和空间变化的敏感性以及光学设计规则,但光谱信息对空间敏感性的影响尚未得到充分探索。我们报告了一种基于信息论的方法,用于量化化学成像中光谱数据的空间定位能力。我们明确考虑了在实验设置中具有重要意义的信噪比和光谱分离的联合效应,以得出红外光谱成像的分辨率极限。