SearcharxivSearch

arXiv subjects

H. Yusuf

Publications and source records attributed to H. Yusuf.

3 recordsLinked to original sources

Measuring the ferromagnetic resonance cone angle via static dipolar fields using diamond spins

We demonstrate quantitative measurement of the ferromagnetic resonance (FMR) precession cone angle of a micro-scale sample of vanadium tetracyanoethylene (V[TCNE]$_{x\sim 2}$) using diamond spins. V[TCNE]$_{x\sim 2}$ is a low-damping, low-magnetization ferrimagnet with potential for scalable spintronics applications. Our study is motivated by the persistent need for quantitative metrology to accurately characterize magnetic dynamics and relaxation. Recently, diamond spins have emerged as sensitive probes of static and dynamic magnetic signals. Unlike analog sensors that require additional calibration, diamond spins respond to magnetic fields via a frequency shift that can be compared with frequency standards. We use a spin echo-based approach to measure the precession-induced change to the static stray dipolar field of a pair of V[TCNE]$_{x\sim 2}$ discs under FMR excitation. Using these stray dipolar field measurements and micromagnetic simulations, we extract the precession cone angle. Additionally, we quantitatively measure the microwave field amplitude using the same diamond spins, thus forming a quantitative link between drive and response. We find that our V[TCNE]$_{x\sim 2}$ sample can be driven to a cone angle of at least 6$^{\circ}$ with a microwave field amplitude of only 0.53 G. This work highlights the power of diamond spins for local, quantitative magnetic characterization.

cond-mat.mtrl-sci

Raman Spectroscopy and Aging of the Low-Loss Ferrimagnet Vanadium Tetracyanoethylene

Vanadium tetracyanoethylene (V[TCNE]$_{x}$, $x\approx 2$) is an organic-based ferrimagnet with a high magnetic ordering temperature $\mathrm{T_C>600 ~K}$, low magnetic damping, and growth compatibility with a wide variety of substrates. However, similar to other organic-based materials, it is sensitive to air. Although encapsulation of V[TCNE]$_{x}$ with glass and epoxy extends the film lifetime from an hour to a few weeks, what is limiting its lifetime remains poorly understood. Here we characterize encapsulated V[TCNE]$_{x}$ films using confocal microscopy, Raman spectroscopy, ferromagnetic resonance and SQUID magnetometry. We identify the relevant features in the Raman spectra in agreement with \textit{ab initio} theory, reproducing $\mathrm{C=C,C\equiv N}$ vibrational modes. We correlate changes in the effective dynamic magnetization with changes in Raman intensity and in photoluminescence. Based on changes in Raman spectra, we hypothesize possible structural changes and aging mechanisms in V[TCNE]$_x$. These findings enable a local optical probe of V[TCNE]$_{x}$ film quality, which is invaluable in experiments where assessing film quality with local magnetic characterization is not possible.

cond-mat.mtrl-sci

Broadband EPR Spectroscopy in Diverse Field Conditions Using Optically Detected Nitrogen-Vacancy Centers in Diamond

Paramagnetic magnetic resonance, a powerful technique for characterizing and identifying chemical targets, is increasingly used for imaging; however, low spin polarization at room temperature and moderate magnetic fields poses challenges for detecting small numbers of spins. In this work, we use fluorescence from nitrogen-vacancy (NV) centers in diamond to detect the electron paramagnetic resonance (EPR) spectrum of optically inactive target spins under various conditions of field magnitude and orientation. The protocol requires neither direct microwave manipulation of the NV spins nor spectral overlap between NV and target spin resonances, thus enabling broadband detection. This unexpected non-resonant coupling is attributable to a two-phonon process that relaxes NV spins proximate to the fluctuating dipole moment of the target spin, suggesting that the sensitivity is determined by the dipole-dipole coupling strength. This approach holds promise for sensitive EPR detection, particularly in settings where control over the diamond-crystal orientation is difficult. This is notably the case for biological sensing applications, where nanodiamonds are being pursued for their bright, stable fluorescence and biocompatibility.

cond-mat.mes-hall