ترغب بنشر مسار تعليمي؟ اضغط هنا

Hyperpolarized relaxometry based nuclear T1 noise spectroscopy in hybrid diamond quantum registers

116   0   0.0 ( 0 )
 نشر من قبل Benjamin Safvati
 تاريخ النشر 2019
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

Understanding the origins of spin lifetimes in hybrid quantum systems is a matter of current importance in several areas of quantum information and sensing. Methods that spectrally map spin relaxation processes provide insight into their origin and can motivate methods to mitigate them. In this paper, using a combination of hyperpolarization and precision field cycling over a wide range (1mT-7T), we map frequency dependent relaxation in a prototypical hybrid system of 13C nuclear spins in diamond coupled to Nitrogen Vacancy centers. Nuclear hyperpolarization through the optically pumped NV electrons allows signal time savings for the measurements exceeding million-fold over conventional methods. We observe that 13C lifetimes show a dramatic field dependence, growing rapidly with field up to 100mT and saturating thereafter. Through a systematic study with increasing substitutional electron (P1 center) concentration as well as 13C enrichment levels, we identify the operational relaxation channels for the nuclei in different field regimes. In particular, we demonstrate the dominant role played by the 13C nuclei coupling to the interacting P1 electronic spin bath. These results pave the way for quantum control techniques for dissipation engineering to boost spin lifetimes in diamond, with applications ranging from engineered quantum memories to hyperpolarized 13C imaging.



قيم البحث

اقرأ أيضاً

We report on the noise spectrum experienced by few nanometer deep nitrogen-vacancy centers in diamond as a function of depth, surface coating, magnetic field and temperature. Analysis reveals a double-Lorentzian noise spectra consistent with a surfac e electronic spin bath, with slower dynamics due to spin-spin interactions and faster dynamics related to phononic coupling. These results shed new light on the mechanisms responsible for surface noise affecting shallow spins at semiconductor interfaces, and suggests possible directions for further studies. We demonstrate dynamical decoupling from the surface noise, paving the way to applications ranging from nanoscale NMR to quantum networks.
Initializing quantum registers with high fidelity is a fundamental precondition for many applications like quantum information processing and sensing. The electronic and nuclear spins of a Nitrogen-Vacancy (NV) center in diamond form an interesting h ybrid quantum register that can be initialized by a combination of laser, microwave, and radio-frequency pulses. However, the laser illumination, which is necessary for achieving electron spin polarization, also has the unwanted side-effect of depolarizing the nuclear spin. Here, we study how the depolarization dynamics of the $^{14}$N nuclear spin depends on the laser wavelength. We show experimentally that excitation with an orange laser (594 nm) causes significantly less nuclear spin depolarization compared to the green laser (532 nm) typically used for excitation and hence leads to higher nuclear spin polarization. This could be because orange light excitation inhibits ionization of NV$^{0}$ into NV$^{-}$ and therefore suppresses one source of noise acting on the nuclear spin.
The dynamical evolution of a quantum register of arbitrary length coupled to an environment of arbitrary coherence length is predicted within a relevant model of decoherence. The results are reported for quantum bits (qubits) coupling individually to different environments (`independent decoherence) and qubits interacting collectively with the same reservoir (`collective decoherence). In both cases, explicit decoherence functions are derived for any number of qubits. The decay of the coherences of the register is shown to strongly depend on the input states: we show that this sensitivity is a characteristic of $both$ types of coupling (collective and independent) and not only of the collective coupling, as has been reported previously. A non-trivial behaviour (recoherence) is found in the decay of the off-diagonal elements of the reduced density matrix in the specific situation of independent decoherence. Our results lead to the identification of decoherence-free states in the collective decoherence limit. These states belong to subspaces of the systems Hilbert space that do not get entangled with the environment, making them ideal elements for the engineering of ``noiseless quantum codes. We also discuss the relations between decoherence of the quantum register and computational complexity based on the new dynamical results obtained for the register density matrix.
We discuss how standard $T_2$-based quantum sensing and noise spectroscopy protocols often give rise to an inadvertent quench of the system or environment being probed: there is an effective sudden change in the environmental Hamiltonian at the start of the sensing protocol. These quenches are extremely sensitive to the initial environmental state, and lead to observable changes in the sensor qubit evolution. We show how these new features can be used to directly access environmental response properties. This enables methods for direct measurement of bath temperature, and methods to diagnose non-thermal equilibrium states. We also discuss techniques that allow one to deliberately control and modulate this quench physics, which enables reconstruction of the bath spectral function. Extensions to non-Gaussian quantum baths are also discussed, as is the direct applicability of our ideas to standard diamond NV-center based quantum sensing platforms.
Nitrogen-vacancy (NV) centers in diamond are promising quantum sensors for their long spin coherence time under ambient conditions. However, their spin resonances are relatively insensitive to non-magnetic parameters such as temperature. A magnetic-n anoparticle-nanodiamond hybrid thermometer, where the temperature change is converted to the magnetic field variation near the Curie temperature, was demonstrated to have enhanced temperature sensitivity (11 mK Hz^{-1/2}) [Phys. Rev. X 8, 011042 (2018)], but the sensitivity was limited by the large spectral broadening of ensemble spins in nanodiamonds. To overcome this limitation, here we showed an improved design of a hybrid nanothermometer using a single NV center in a diamond nanopillar coupled with a single magnetic nanoparticle of copper-nickel alloy, and demonstrated a temperature sensitivity of 76 uK Hz^{-1/2}. This hybrid design enabled detection of 2 millikelvins temperature changes with temporal resolution of 5 milliseconds. The ultra-sensitive nanothermometer offers a new tool to investigate thermal processes in nanoscale systems.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا