Intensity calculations

From Vacuum Ultra Violet
Revision as of 08:12, 2 November 2022 by Mnuland@nikhef.nl (talk | contribs) (Add statistics details)
Jump to navigation Jump to search

Intensity of light in the VUV setup

https://www.photonics.com/Article.aspx?AID=56745 for a nice comparison of nitrogen and vacuum VUV systems.

Estimate of detectable fluorescence levels

We will estimate how much a material has to fluoresce in order for us to be able to see this signal above the dark count rate of the SiPMs. We will assume here that we use the visible SiPMs, that they have a geometric fill factor of 65% and are placed at 1 cm from the sample. We will also assume they have a light collection efficiency of 25%. Furthermore, we take the dark count rate to be the maximum (according to the datasheet) of 6 Mcps. Dark counts have a Poisson distribution. With a mean of 6 Mcps, we can approximate the Poisson distribution by a normal distribution with a mean of 6 Mcps, and a standard deviation of sqrt(6e6).

We'll do some very naive statistics here, taking only a single measurement of the fluorescence signal. If we want to be able to say with p≤0.05 that we have seen a signal, we'll need to measure at least 6e6 + 1.65*sqrt(6e6) = 6004042 counts, according to the one-sided z-test values table. As the two SiPMs are 6x6mm, they have a surface area of 72 mm^2. If they are positioned at 1 cm from the sample, we have a solid angle coverage of approximately 5%. Taking into account the geometric fill factor and the photon detection efficiency, we get that we need to get at least 500,000 fluoresced photons per second from the sample in order to measure the 4042 counts above the dark count rate.

Now, let's make a wild guess, and say that the deuterium lamp is a light bulb of 60W (the power supply is 200 W). If it would emit only at 200 nm, the 60 W would correspond to 6*10^19 photons per second, using E=hc/lambda. But of course we emit a spectrum, and then select a single wavelength. We have some geometric factors to take into account, as well as losses due to the slits and the grating, and also air attenuation. So, let us say we irradiate our sample with only 10^12 photons per second. Then the required 500,000 fluoresced photons, correspond to a fluorescence level of ~10^-4%.

This is what I did for the air attenuation, Marjoleins caclulations for the pressure were a big help.

Intensity of light in the XENON detector

This section describes the first estimates for the level of fluorescence required to explain the single electron signals which are observed after a larger event in the TPC, also named electron trains.

It has been suggested [1] that the fluorescence of PTFE reflectors in the XENON100 and XENON1T detectors could explain the presence of a delayed single electron component. The signal is observed with a delay time of 2.3 ms after a larger observed pulse and could be described by ionisation of oxygen atoms or impurities upon the absorption of a fluoresced photon from the PTFE. This photon would need to be in the infrared region and therefore invisible to the PMTs in the detector, but in principle could have enough energy to liberate electrons upon absorption.

This statement is taken as a basis for the initial estimation into how much the PTFE in the XENON detector would need to fluoresce in order to be a viable candidate for the origin of this observed background. PTFE has been shown to fluoresce in the visible region [2-6] between 250 nm and 500 nm at room temperature as shown in Figure 1. The cryogenic, low-temperature effect of PTFE fluorescence spectra is yet unknown.

Figure 1: Spectral response of PTFE integrating spheres under 220nm light, offset for readability [2].
Integrating sphere spectra.png

The distribution shown in Figure 2 indicates that most single electron signals are detected with roughly 15 PE with a maximum count around 475 per electron train. We will take this as a starting number for these initial calculations. [7] indicates that these trains can occur with up to 10^6 single electron signals.

Figure 2: The green area shows the single electron response with an extraction field of 5.9 kV [7].
Electron train spectra.png

The energy required to ionise an oxygen molecule is 0.45 eV, so any photon released during fluorescence with a wavelength up to 2 um would be energetic enough to ionise. This is well within a reasonable energy range for fluorescence observed from PTFE previously. The reflectivity of PTFE is given as 95% in [8], so we will (conservatively) assume that 5% of the photons that hit the detector walls are absorbed and can be fluoresced. The next assumption we will make is that the initial event occurred in the centre of the detector, giving the PMT solid angle coverage in XENON1T as roughly 50%.

Electron trains follow many different events in the detector from radioactivity events to scattering events. For this example, we will assume that the initial event produces 10^6 scintillation photons. Therefore, if 50% of these photons collide with the detector wall and 5% of those photons are absorbed for fluorescence, to reach the 475 single electrons in the train, the PTFE would require a fluorescence quantum yield of 0.02.

The Light Collection Efficiency (LCE) of the top PMT array in XENONnT is shown in Figure 3. This averages at 35% due to the reflective properties of the interface between liquid and gaseous xenon. Whilst this is shown for XENONnT, it is very similar to the XENON1T LCE levels. Using this number, the fluorescence quantum yield is increased to 0.06.

Figure 3: The LCE map of XENONnT, with the average sitting at 35\% [9].
LCE XENONnT.png

We shall conservatively assume that only 50% of the fluoresced photons go on to ionise oxygen molecules in the liquid xenon volume. This also increases the fluorescence quantum yield to nearly 0.11.

Conclusion:

We therefore require 11% of the absorbed photons from an event of 10^6 photons to be fluoresced in order to explain the origin of the 475 single electron signal peak observed in electron trains.

References

References
Reference number Reference
1 P. Sorensen and K. Kamdin, “Two distinct components of the delayed single electron noise in

liquid xenon emission detectors,” Journal of Instrumentation, vol. 13, pp. P02032–P02032, feb 2018.

2 P. Shaw, Z. Li, U. Arp, and K. Lykke, “Ultraviolet characterization of integrating spheres”, Applied optics, vol. 46, pp. 5119–28, 2007
3 E. Peik, “Long-lasting photoluminescence in polymers,” Hournal of Physics D: Applied Physics,

vol. 40, no. 11, pp. 3330–3334, 2007

4 P. Shaw, Z. Li, U. Arp, and K. Lykke, “Ultraviolet characterization of integrating spheres,”, Applied optics, vol. 46, pp. 5119–28, 2007 10
5 G. Araujo, "Wavelength Shifting and Photon Detection of Scintillation Light from Liquid Argon", PhD thesis, 03 2019
6 Araujo, G. R., Pollmann, T., Ulrich, A., "Photoluminescence response of acrylic (pmma) and polytetrafluo-roethylene (ptfe) to ultraviolet light,” The European Physical Journal C, vol. 653 79 8, pp. 1434–

6052, 2019

7 A. Kopec, “Extraction field effect on electron train backgrounds in asterix”, XENON wiki
8 Cyril, “Study of lce with the v305 of the code,”, XENON wiki
9 The XENON Collaboration, "Projected WIMP sensitivity of the XENONnT dark matter experiment,”

Journal of Cosmology and Astroparticle Physics, vol. 2020, pp. 031–031, nov 2020.