We present a novel method to determine the resonant frequency and quality factor of microwave resonators which is faster, more stable, and conceptually simpler than the yet existing techniques. The microwave resonator is irradiated at a frequency away from its resonance. It then emits an exponentially decaying radiation at its eigen-frequency when the excitation is rapidly switched off. The emission is down-converted with a microwave mixer, digitized and its Fourier transformation (FT) directly yields the resonance curve in a single shot. Being an FT based method, this technique possesses the Fellgett (multiplex) and Connes (accuracy) advantages and it conceptually mimics that of pulsed nuclear magnetic resonance. We also establish a novel benchmark to compare accuracy of the different approaches of microwave resonator measurements. This shows that the present method have similar accuracy to the existing ones.

We present the development and performance of a Fourier transformation (FT) based Raman spectrometer working with visible laser (532 nm) excitation. It is generally thought that FT-Raman spectrometers are not viable in the visible range where shot-noise limits the detector performance and therein they are outperformed by grating based, dispersive ones. We show that contrary to this common belief, the recent advances of high-performance interference filters makes the FT-Raman design a valid alternative to dispersive Raman spectrometers for samples which do not luminesce. We critically compare the performance of our spectrometer to two dispersive ones: a home-built single channel and a state-of-the-art CCD based instruments. We demonstrate a similar or even better sensitivity than the CCD based dispersive spectrometer particularly when the laser power density is considered. The instrument possesses all the known advantages of the FT principle of spectral accuracy, high throughput, and economic design. We also discuss the general considerations which helps the community reassess the utility of the different Raman spectrometer designs.

There is now compelling evidence that the normal state of superconducting overdoped cuprates is a strange metal comprising two distinct charge sectors, one governed by coherent quasiparticle excitations, the other seemingly incoherent and characterized by non-quasiparticle (Planckian) dissipation. The zero-temperature superfluid density n_s(0)ns(0) of overdoped cuprates exhibits an anomalous depletion with increased hole doping pp, falling to zero at the edge of the superconducting dome. Over the same doping range, the effective zero-temperature Hall number n_{\rm H}(0) transitions from pp to 1 + pp. By taking into account the presence of these two charge sectors, we demonstrate that in the overdoped cuprates Tl_22Ba_22CuO_{6+\delta}6+δ and La_{2-x}2−xSr_xxCuO_44, the growth in n_s(0)ns(0) as pp is decreased from the overdoped side may be compensated by the loss of carriers in the coherent sector. Such a correspondence is contrary to expectations from conventional BCS theory and implies that superconductivity in overdoped cuprates emerges uniquely from the sector that exhibits incoherent transport in the normal state.

The free electron laser Free electron Laser for Advanced spectroscopy and high Resolution Experiments (FLARE) at the FELIX Laboratory generates powerful radiation in the frequency range of 0.3–3 THz. This light, in combination with 33 T Bitter magnets at the High Field Magnet Laboratory, provides the unique opportunity to perform THz magneto spectroscopy with light intensities many orders of magnitude higher than provided by conventional sources. The performance of the THz spectrometer is measured via high-field electron spin resonance (ESR) in the paramagnetic benchmark system 2,2-diphenyl-1-picrylhydrazyl (DPPH). The narrow ESR linewidth of DPPH allows us to resolve a fine structure with 3 GHz spacing, demonstrating a considerable coherence of the individual THz micropulses of FLARE. The spectral resolution Δν/ν is better than 0.1%, which is an order of magnitude higher than typical values for a rf-linac based free electron laser. The observed coherence of the high power THz micropulses is a prerequisite for resonant control of matter, such as THz electron spin echo spectroscopy.

The magnetostriction phenomenon, which exists in almost all magnetically ordered materials, is proved to have wide application potential in precision machinery, microdisplacement control, robotics, and other high‐tech fields. Understanding the microscopic mechanism behind the magnetostrictive properties of magnetically ordered compounds plays an essential role in realizing technological applications and helps the fundamental understanding of magnetism and superconductivity. In paramagnets, however, the magnetostriction is usually significantly smaller because of the magnetic disorder. Here, the observation of a remarkably strong magnetostrictive response of the insulator paramagnet KEr(MoO4)2 is reported on. Using low‐temperature magnetization and dilatometry measurements, in combination with ab initio calculations, employing a quasi‐atomic treatment of many‐body effects, it is demonstrated that the magnetostriction anomaly in KEr(MoO4)2 is driven by a single‐ion effect. This analysis reveals a strong coupling between the Er3+ ions and the crystal lattice due to the peculiar behavior of the magnetic quadrupolar moments of Er3+ ions in the applied field, shedding light on the microscopic mechanism behind the massive magnetostrictive response.