Metallic magnetic micro-calorimeters (MMCs) operated at millikelvin temperature offer the possibility to achieve eV-scale energy resolution with high stopping power for X-rays and massive particles in an energy range up to several tens of keV. This motivates their use in a wide range of applications in fields as particle physics, atomic and molecular physics. Present detector systems consist of MMC arrays read out by 32 two-stage SQUID read-out channels. In contrast to the design of the detector array and consequently the design of the front-end SQUIDs, which need to be optimised for the physics case and the particles to be detected in a given experiment, the read-out chain can be standardised. We present our new standardised 32-channel parallel read-out for the operation of MMC arrays to be operated in a dilution refrigerator. The read-out system consists of a detector module, whose design depends on the particular application, an amplifier module, ribbon cables from room temperature to the millikelvin platform and a data acquisition system. In particular, we describe the realisation of the read-out system prepared for the ECHo-1k experiment for the operation of two 64-pixel arrays. The same read-out concept is also used for the maXs detector systems, developed for the study of the de-excitation of highly charged heavy ions by X-rays, as well as for the MOCCA system, developed for the energy and position sensitive detection of neutral molecular fragments for the study of fragmentation when molecular ions recombine with electrons. The choice of standard modular components for the operation of 32-channel MMC arrays offer the flexibility to upgrade detector modules without the need of any changes in the read-out system and the possibility to individually exchange parts in case of damages or failures.

We have systematically investigated the energy resolution of a magnetic micro-calorimeter (MMC) for atomic and molecular projectiles at impact energies ranging from E ≈ 13 to 150 keV. For atoms we obtained absolute energy resolutions down to ∆E ≈ 120 eV and relative energy resolutions down to ∆E/E ≈ 10 −3 . We also studied in detail the MMC energy-response function to molecular projectiles of up to mass 56 u. We have demonstrated the capability of identifying neutral fragmentation products of these molecules by calorimetric mass spectrometry. We have modeled the MMC energy-response function for molecular projectiles and conclude that backscattering is the dominant source of the energy spread at the impact energies investigated. We have successfully demonstrated the use of a detector absorber coating to suppress such spreads. We briefly outline the use of MMC detectors in experiments on gas-phase collision reactions with neutral products. Our findings are of general interest for mass spectrometric techniques, particularly for those desiring to make neutral-particle mass measurements.

We report on the first integration of novel metallic magnetic (micro-) calorimeter detectors, developed within SPARC (Stored Particles Atomic Physics Research Collaboration), into the experimental environment of storage rings at GSI, Darmstadt, namely at the electron cooler of CRYRING@ESR. Two of these detector systems were positioned at the 0° and 180° view ports of the cooler section to obtain high-resolution x-ray spectra originating from a stored beam of hydrogen-like uranium interacting with the cooler electrons. While previous test measurements with microcalorimeters at the accelerator facility of GSI were conducted in the mode of well-established stand-alone operation, for the present experiment we implemented several notable modifications to exploit the full potential of this type of detector for precision x-ray spectroscopy of stored heavy ions. Among these are a new readout system compatible with the multi branch system data acquisition platform of GSI, the synchronization of a quasi-continuous energy calibration with the operation cycle of the accelerator facility, as well as the first exploitation of the maXs detectors’ time resolution to apply coincidence conditions for the detection of photons and charge-changed ions.