Raman spectroscopy allows nondestructive analysis of materials using laser illumination. However, most Raman spectrometers can only provide good signal levels and sufficient spectral resolution, by focusing the laser to micrometer-sized spots. This equates to enormous laser intensities, which for samples with even very minor optical absorption either means destroying or damaging it by absorbing even a tiny fraction of the laser power, or it means reducing the laser intensity and hence the signal level. Furthermore, Raman signals generated above or below the focal plane are rejected in traditional Raman spectrometers. As signal levels are already extremely low in Raman spectroscopy, several schemes offer an alternative to focusing down to a diffraction-limited spot, to increase the area by up to 6 orders of magnitude, and increase the sampling depth. This review describes and compares these schemes, and estimates the typical illumination areas.
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Andrew Downes (2019) studied this question.
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