The present paper reports on a Finite Element Method (FEM) analysis of the experimental situation corresponding to the measurement of the temperature variation in a single cell plated on bulk diamond by means of optical techniques. Starting from previous experimental results, we have determined—in a uniform power density approximation and under steady-state conditions—the total heat power that has to be dissipated by a single cell plated on a glassy substrate in order to induce the typical maximum temperature increase DTglass = 1 K. While keeping all of the other parameters constant, the glassy substrate has been replaced by a diamond plate. The FEM analysis shows that, in this case, the maximum temperature increase is expected at the diamond/cell interface and is as small as DTdiam = 4.6 × 10−4 K. We have also calculated the typical decay time in the transient scenario, which resulted in t ≈ 250 μs. By comparing these results with the state-of-the-art sensitivity values, we prove that the potential advantages of a longer coherence time, better spectral properties, and the use of special field alignments do not justify the use of diamond substrates in their bulk form.
Limitations of Bulk Diamond Sensors for Single-Cell Thermometry
Alessio, A.First
;Truccato, M.Last
2024-01-01
Abstract
The present paper reports on a Finite Element Method (FEM) analysis of the experimental situation corresponding to the measurement of the temperature variation in a single cell plated on bulk diamond by means of optical techniques. Starting from previous experimental results, we have determined—in a uniform power density approximation and under steady-state conditions—the total heat power that has to be dissipated by a single cell plated on a glassy substrate in order to induce the typical maximum temperature increase DTglass = 1 K. While keeping all of the other parameters constant, the glassy substrate has been replaced by a diamond plate. The FEM analysis shows that, in this case, the maximum temperature increase is expected at the diamond/cell interface and is as small as DTdiam = 4.6 × 10−4 K. We have also calculated the typical decay time in the transient scenario, which resulted in t ≈ 250 μs. By comparing these results with the state-of-the-art sensitivity values, we prove that the potential advantages of a longer coherence time, better spectral properties, and the use of special field alignments do not justify the use of diamond substrates in their bulk form.File | Dimensione | Formato | |
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