Parahydrogen Cooling of Nuclear Spin Chains at Hypogeomagnetic Fields
- URL: http://arxiv.org/abs/2606.09649v1
- Date: Mon, 08 Jun 2026 15:40:59 GMT
- Title: Parahydrogen Cooling of Nuclear Spin Chains at Hypogeomagnetic Fields
- Abstract summary: Solution-state molecular nuclear spin networks are promising quantum simulators because their scalar-coupling Hamiltonians are chemically programmable, precisely measurable, and coherent at room temperature.<n>Here, we use parahydrogen-based Signal Amplification by Reversible Exchange (SABRE) to hyperpolarize the chemically engineered 12-spin chain [U-13C,15N]-butyronitrile.<n>SABRE generates percent-level 13C and 15N polarization and prepares non-equilibrium multi-spin orders across the network.
- Score: 35.29742953849465
- License: http://creativecommons.org/licenses/by-nc-nd/4.0/
- Abstract: Solution-state molecular nuclear spin networks are promising quantum simulators because their scalar-coupling Hamiltonians are chemically programmable, precisely measurable, and coherent at room temperature. Their main limitation for quantum information science is initialization: thermal Boltzmann polarization produces highly mixed, high-entropy states. Here, we use parahydrogen-based Signal Amplification by Reversible Exchange (SABRE) at hypogeomagnetic fields (i.e., magnetic fields below Earth field) to hyperpolarize the chemically engineered 12-spin chain [U-13C,15N]-butyronitrile. SABRE generates percent-level 13C and 15N polarization and prepares non-equilibrium multi-spin orders across the network. A von Neumann entropy analysis of such a hyperpolarized system shows that, at the optimal transfer field of 0.52 uT, the full spin system could reach S/k = 8.274, compared with S/k = 8.318 for the unpolarized reference, giving (S-Sth)/k = -0.043. Experimentally, nuclear spin temperatures of 52 mK and 257 mK are achieved for 15N and 13C subensembles, respectively. The larger entropy deficit of the full network than of individual subsystems indicates correlated multi-spin order beyond single-spin polarizations. Rapid field cycling to 9.4 T enables site-resolved NMR readout, while the precisely determined coupling network provides an experimentally benchmarked Hamiltonian for testing quantum-simulation, quantum-control, and Hamiltonian-learning protocols.
Related papers
- Precision hyperfine spectroscopy of an individual nuclear-spin-9/2 [0.0]
Single-spin magnetic resonance spectroscopy promises to yield structural and chemical information at the level of individual atoms or molecules.<n>Here, we use an Er3+ paramagnetic center in a CaWO4 crystal to measure the NMR spectrum of a proximal individual nuclear-spin-9/2 93Nb impurity.<n>We harness the high spectral resolution of our measurements to establish the presence of two previously unobserved terms in the spin Hamiltonian.
arXiv Detail & Related papers (2026-05-04T17:32:57Z) - High-Field NMR Characterization and Indirect $J$-Spectroscopy of a Nuclear Spin Chain [U-$^{13}$C,$^{15}$N]-butyronitrile [35.29742953849465]
One-dimensional chains of coupled spins are minimal models of strongly correlated quantum matter.<n>We present [U-$13$C,$15$N]-butyronitrile as a chemically engineered nuclear spin chain.<n>Our results establish [U-$13$C,$15$N]-butyronitrile as an extremely well-characterized spin chain model system.
arXiv Detail & Related papers (2026-02-14T21:35:34Z) - Finite Spinon Density-of-States in Triangular-Lattice Delafossite TlYbSe$_2$ [4.737474570094059]
We introduce the rare-earth delafossite compound TlYbSe$$ -- extending the search for quantum spin liquids in triangular lattice magnets.<n>Heat capacity measurements reveal no signs of long-range magnetic order down to 20 mK, indicating a quantum-disordered ground state.<n>The results establish the low-temperature, low-field regime of TlYbSe$$ as a prime candidate for field-tunable triangular quantum spin liquid behavior.
arXiv Detail & Related papers (2025-04-07T18:59:51Z) - Spin decoherence in VOPc@graphene nanoribbon complexes [5.691318972818067]
Carbon nanoribbon or nanographene qubit arrays can facilitate quantum-to-quantum transduction between light, charge, and spin.
We study spin decoherence due to coupling with a surrounding nuclear spin bath of an electronic molecular spin of a vanadyl phthalocyanine (VOPc) molecule integrated on an armchair-edged graphene nanoribbon (GNR)
We find that the decoherence time $T$ is anisotropic with respect to magnetic field orientation and determined only by nuclear spins on VOPc and GNR.
arXiv Detail & Related papers (2023-07-31T04:55:05Z) - Thermal masses and trapped-ion quantum spin models: a self-consistent approach to Yukawa-type interactions in the $λ\!φ^4$ model [44.99833362998488]
A quantum simulation of magnetism in trapped-ion systems makes use of the crystal vibrations to mediate pairwise interactions between spins.
These interactions can be accounted for by a long-wavelength relativistic theory, where the phonons are described by a coarse-grained Klein-Gordon field.
We show that thermal effects, which can be controlled by laser cooling, can unveil this flow through the appearance of thermal masses in interacting QFTs.
arXiv Detail & Related papers (2023-05-10T12:59:07Z) - Anisotropic electron-nuclear interactions in a rotating quantum spin
bath [55.41644538483948]
Spin-bath interactions are strongly anisotropic, and rapid physical rotation has long been used in solid-state nuclear magnetic resonance.
We show that the interaction between electron spins of nitrogen-vacancy centers and a bath of $13$C nuclear spins introduces decoherence into the system.
Our findings offer new insights into the use of physical rotation for quantum control with implications for quantum systems having motional and rotational degrees of freedom that are not fixed.
arXiv Detail & Related papers (2021-05-16T06:15:00Z) - Controlled coherent dynamics of [VO(TPP)], a prototype molecular nuclear
qudit with an electronic ancilla [50.002949299918136]
We show that [VO(TPP)] (vanadyl tetraphenylporphyrinate) is a promising system suitable to implement quantum computation algorithms.
It embeds an electronic spin 1/2 coupled through hyperfine interaction to a nuclear spin 7/2, both characterized by remarkable coherence.
arXiv Detail & Related papers (2021-03-15T21:38:41Z) - Broad-band spectroscopy of a vanadyl porphyrin: a model electronuclear
spin qudit [0.0]
We show that each molecule fulfills the conditions to act as a universal 4-qubit processor or, equivalently, as a d = 16 qudit.
These findings widen the catalogue of chemically designed systems able to implement non-trivial quantum functionalities.
arXiv Detail & Related papers (2021-01-27T19:12:23Z) - Electrically tuned hyperfine spectrum in neutral
Tb(II)(Cp$^{\rm{iPr5}}$)$_2$ single-molecule magnet [64.10537606150362]
Both molecular electronic and nuclear spin levels can be used as qubits.
In solid state systems with dopants, an electric field was shown to effectively change the spacing between the nuclear spin qubit levels.
This hyperfine Stark effect may be useful for applications of molecular nuclear spins for quantum computing.
arXiv Detail & Related papers (2020-07-31T01:48:57Z) - Optically pumped spin polarization as a probe of many-body
thermalization [50.591267188664666]
We study the spin diffusion dynamics of 13C in diamond, which we dynamically polarize at room temperature via optical spin pumping of engineered color centers.
We find good thermal contact throughout the nuclear spin bath, virtually independent of the hyperfine coupling strength.
Our results open intriguing opportunities to study the onset of thermalization in a system by controlling the internal interactions within the bath.
arXiv Detail & Related papers (2020-05-01T23:16:33Z) - Hyperfine and quadrupole interactions for Dy isotopes in DyPc$_2$
molecules [77.57930329012771]
Nuclear spin levels play an important role in understanding magnetization dynamics and implementation and control of quantum bits in lanthanide-based single-molecule magnets.
We investigate the hyperfine and nuclear quadrupole interactions for $161$Dy and $163$Dy nucleus in anionic DyPc$.
arXiv Detail & Related papers (2020-02-12T18:25:31Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.