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Register a new userElectron Spin Resonance spectroscopy with femtoliter detection volume
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We report electron spin resonance measurements of donors in silicon at millikelvin temperatures using a superconducting $LC$ planar micro-resonator and a Josephson Parametric Amplifier. The resonator includes a nanowire inductor, defining a femtoliter detection volume. Due to strain in the substrate, the donor resonance lines are heavily broadened. Single-spin to photon coupling strengths up to $sim 3~text{kHz}$ are observed. The single shot sensitivity is $120 pm 24~$spins/Hahn echo, corresponding to $approx 12 pm 3$~spins$/sqrt{text{Hz}}$ for repeated acquisition.
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We report electron spin resonance spectroscopy measurements performed at millikelvin temperatures in a custom-built spectrometer comprising a superconducting micro-resonator at $7$ GHz and a Josephson parametric amplifier. Owing to the small ${sim}10^{-12}lambda^3$ magnetic resonator mode volume and to the low noise of the parametric amplifier, the spectrometer sensitivity reaches $260pm40$ spins$/$echo and $65pm10$ $mathrm{spins}/sqrt{text{Hz}}$, respectively.
We report the nanoscale spin detection and electron paramagnetic resonance (EPR) spectrum of copper (Cu$^{2+}$) ions via double electron-electron resonance with single spins in diamond at room temperature and low magnetic fields. We measure unexpectedly narrow EPR resonances with linewidths $sim 2-3$ MHz from copper-chloride molecules dissolved in poly-lysine. We also observe coherent Rabi oscillations and hyperfine splitting from single Cu$^{2+}$ ions, which could be used for dynamic nuclear spin polarization and higher sensitivity of spin detection. We interpret and analyze these observations using both spin hamiltonian modeling of the copper-chloride molecules and numerical simulations of the predicted DEER response, and obtain a sensing volume $sim (250 text{nm})^3$. This work will open the door for copper-labeled EPR measurements under ambient conditions in bio-molecules and nano-materials.
A new method for detecting the magnetic resonance of electronic spins at low temperature is demonstrated. It consists in measuring the signal emitted by the spins with a superconducting qubit that acts as a single-microwave-photon detector, resulting in an enhanced sensitivity. We implement this new type of electron-spin resonance spectroscopy using a hybrid quantum circuit in which a transmon qubit is coupled to a spin ensemble consisting of NV centers in diamond. With this setup we measure the NV center absorption spectrum at 30mK at an excitation level of thicksim15,mu_{B} out of an ensemble of 10^{11} spins.
We report on electron spin resonance spectroscopy measurements using a superconducting flux qubit with a sensing volume of 6 fl. The qubit is read out using a frequency-tunable Josephson bifurcation amplifier, which leads to an inferred measurement sensitivity of about 20 spins in a 1 s measurement. This sensitivity represents an order of magnitude improvement when compared with flux-qubit schemes using a dc-SQUID switching readout. Furthermore, noise spectroscopy reveals that the sensitivity is limited by flicker ($1/f$) flux noise.
Electron spin resonance (ESR) spectroscopy has broad applications in physics, chemistry and biology. As a complementary tool, zero-field ESR (ZF-ESR) spectroscopy has been proposed for decades and shown its own benefits for investigating the electron fine and hyperfine interaction. However, the ZF-ESR method has been rarely used due to the low sensitivity and the requirement of much larger samples than conventional ESR. In this work, we present a method for deploying ZF-ESR spectroscopy at the nanoscale by using a highly sensitive quantum sensor, the nitrogen-vacancy center in diamond. We also measure the nanoscale ZF-ESR spectrum of a few P1 centers in diamond, and show that the hyperfine coupling constant can be directly extracted from the spectrum. This method opens the door to practical applications of ZF-ESR spectroscopy, such as investigation of the structure and polarity information in spin-modified organic and biological systems.
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