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Superconducting On-chip Fourier Transform Spectrometers (SOFTS) are broadband, compact and electronic interferometers. Being extremely compact, SOFTS can fit into standard antenna coupled detector architectures. SOFTS will enable kilo-pixel spectro-imaging focal planes enhancing sub-millimeter science; particularly cluster astrophysics / cosmology, CMB-science and line intensity mapping. This proceeding details the development, design and bench-marking of RF on-chip architecture of SOFTS for Ka and W bands.

Ground-based cosmic microwave background (CMB) experiments are undergoing a period of exponential growth. Current experiments are observing with 1000–10,000 detectors, and the next-generation experiment (CMB stage 4) is proposing to deploy approximately 500,000 detectors. This order of magnitude increase in detector count will require a new approach for readout electronics. We have developed superconducting resonators for next-generation frequency-domain multiplexing (fMUX) readout architecture. Our goal is to reduce the physical size of resonators, such that resonators and detectors can eventually be integrated on a single wafer. To reduce the size of these resonators, we have designed spiral inductors and interdigitated capacitors that resonate around 10–100 MHz, an order of magnitude higher frequency compared to current fMUX readout systems. The higher frequency leads to a wider bandwidth and would enable higher multiplexing factor than the current $$\sim $$ 50 detectors per readout channel. We will report on the simulation, fabrication method, characterization technique, and measurement of quality factor of these resonators.

The electrooxidation of Gabapentin was studied on nanotubes of nickel oxide-modified carbon paste electrode for the first time. Cyclic voltammetry was employed to investigate the electrooxidation process. A simple, sensitive, and efficient amperometric method was developed for the analysis of the drug, and the corresponding analytical parameters were reported. For Gabapentin, a detection limit of 0.3 μM was obtained in a linear range of 2.4–50 μM. The proposed amperometric method was also applied to the analysis of commercial capsules, and the results were in good agreement with the declared values. Also, the applicability of the method to the direct assay of the drug in human serum and urine was described.

The electrochemical behavior of sodium alendronate on copper microparticle- and copper nanoparticle-modified carbon paste electrodes was investigated. In the voltammograms recorded using microparticles, a single anodic oxidation peak appeared, while using nanoparticles, two anodic peaks appeared. The anodic currents were related to the electrocatalytic oxidation of alendronate via the active species of Cu(III). The catalytic rate constant for the electrocatalytic oxidation process and the diffusion coefficient of alendronate were obtained to be 1.57 × 103 cm3 mol−1 s−1 and 2.44 × 10−6 cm2 s−1, respectively. A sensitive and time-saving detection procedure was developed for the analysis of alendronate, and the corresponding analytical parameters were reported. Alendronate was determined with a limit of detection of 11.26 μmol L−1 with a linear range of 50–6,330 μmol L−1. The proposed amperometric method was applied to the analysis of commercial pharmaceutical tablets, and the results were in good agreement with the declared values.