Search

The nonlinear energy response of cryogenic microcalorimeters is usually corrected through an empirical calibration. X-ray or gamma-ray emission lines of known shape and energy anchor a smooth function that generalizes the calibration data and converts detector measurements to energies. We argue that this function should be an approximating spline. The theory of Gaussian process regression makes a case for this functional form. It also provides an important benefit previously absent from our calibration method: a quantitative uncertainty estimate for the calibrated energies, with lower uncertainty near the best-constrained calibration points., Comment: Submitted to J. Low Temperature Physics for the Proceedings of the 19th International Workshop on Low-Temperature Detectors (2021)

A principal component analysis (PCA) of clean microcalorimeter pulse records can be a first step beyond statistically optimal linear filtering of pulses towards a fully non-linear analysis. For PCA to be practical on spectrometers with hundreds of sensors, an automated identification of clean pulses is required. Robust forms of PCA are the subject of active research in machine learning. We examine a version known as coherence pursuit that is simple, fast, and well matched to the automatic identification of outlier records, as needed for microcalorimeter pulse analysis., Comment: Accepted in J. Low Temperature Physics

We consider how to analyze microcalorimeter pulses for quantities that are nonlinear in the data, while preserving the signal-to-noise advantages of lin- ear optimal filtering. We successfully apply our chosen approach to compute the electrothermal feedback energy deficit (the "Joule energy") of a pulse, which has been proposed as a linear estimator of the deposited photon energy., Comment: Accepted by Journal of Low Temperature Physics. Contribution to the proceedings of Low Temperature Detectors 17, (Kurume Japan, 2017)

We introduce a new technique for determining x-ray fluorescence line energies and widths, and we present measurements made with this technique of 22 x-ray L lines from lanthanide-series elements. The technique uses arrays of transition-edge sensors, microcalorimeters with high energy-resolving power that simultaneously observe both calibrated x-ray standards and the x-ray emission lines under study. The uncertainty in absolute line energies is generally less than 0.4 eV in the energy range of 4.5 keV to 7.5 keV. Of the seventeen line energies of neodymium, samarium, and holmium, thirteen are found to be consistent with the available x-ray reference data measured after 1990; only two of the four lines for which reference data predate 1980, however, are consistent with our results. Five lines of terbium are measured with uncertainties that improve on those of existing data by factors of two or more. These results eliminate a significant discrepancy between measured and calculated x-ray line energies for the terbium Ll line (5.551 keV). The line widths are also measured, with uncertainties of 0.6 eV or less on the full-width at half-maximum in most cases. These measurements were made with an array of approximately one hundred superconducting x- ray microcalorimeters, each sensitive to an energy band from 1 keV to 8 keV. No energy-dispersive spectrometer has previously been used for absolute-energy estimation at this level of accuracy. Future spectrometers, with superior linearity and energy resolution, will allow us to improve on these results and expand the measurements to more elements and a wider range of line energies., Comment: This version is the one accepted for publication in Metrologia

The so-called "optimal filter" analysis of a microcalorimeter's x-ray pulses is statistically optimal only if all pulses have the same shape, regardless of energy. The shapes of pulses from a nonlinear detector can and do depend on the pulse energy, however. A pulse-fitting procedure that we call "tangent filtering" accounts for the energy dependence of the shape and should therefore achieve superior energy resolution. We take a geometric view of the pulse-fitting problem and give expressions to predict how much the energy resolution stands to benefit from such a procedure. We also demonstrate the method with a case study of K-line fluorescence from several 3d transition metals. The method improves the resolution from 4.9 eV to 4.2 eV at the Cu K$\alpha$ line (8.0keV)., Comment: Submitted to the Proceedings of the 2016 Applied Superconductivity Conference

The analysis of data from x-ray microcalorimeters requires great care; their excellent intrinsic energy resolution cannot usually be achieved in practice without a statistically near-optimal pulse analysis and corrections for important systematic errors. We describe the essential parts of a pulse-analysis pipeline for data from x-ray microcalorimeters, including steps taken to reduce systematic gain variation and the unwelcome dependence of filtered pulse heights on the exact pulse-arrival time. We find these steps collectively to be essential tools for getting the best results from a microcalorimeter-based x-ray spectrometer., Comment: Accepted for publication in J. Low Temperature Physics, special issue for the proceedings of the Low Temperature Detectors 16 conference

Transition edge sensor microcalorimeters can measure x-ray and gamma-ray energies with very high energy resolution and high photon-collection efficiency. For this technology to reach its full potential in future x-ray observatories, each sensor must be able to measure hundreds or even thousands of photon energies per second. Current "optimal filtering" approaches to achieve the best possible energy resolution work only for photons well isolated in time, a requirement in direct conflict with the need for high-rate measurements. We describe a new analysis procedure to allow fitting for the pulse height of all photons even in the presence of heavy pulse pile-up. In the limit of isolated pulses, the technique reduces to the standard optimal filtering with long records. We employ reasonable approximations to the noise covariance function in order to render multi-pulse fitting computationally viable even for very long data records. The technique is employed to analyze x-ray emission spectra at 600 eV and 6 keV at rates up to 250 counts per second in microcalorimeters having exponential signal decay times of approximately 1.2 ms., Comment: This version exactly matches the submission to journal

We introduce a filter-construction method for pulse processing that differs in two respects from that in standard optimal filtering, in which the average pulse shape and noise-power spectral density are combined to create a convolution filter for estimating pulse heights. First, the proposed filters are computed in the time domain, to avoid periodicity artifacts of the discrete Fourier transform, and second, orthogonality constraints are imposed on the filters, to reduce the filtering procedure's sensitivity to unknown baseline height and pulse tails. We analyze the proposed filters, predicting energy resolution under several scenarios, and apply the filters to high-rate pulse data from gamma-rays measured by a transition-edge-sensor microcalorimeter., Comment: 5 pages, 6 figures, 1 table