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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 2025 Jan 8;122(2):e2422156122. doi: 10.1073/pnas.2422156122

Superconducting critical temperature elevated by intense magnetic fields

Z Wu a, H Chen a, T I Weinberger a, A Cabala b, D E Graf c, Y Skourski d, W Xie e, Y Ling e, Z Zhu e, V Sechovský b, M Vališka b, F M Grosche a, A G Eaton a,1
PMCID: PMC11745342  PMID: 39773022

Abstract

Below a critical temperature Tc, superconductors transport electrical charge without dissipative energy losses. The application of a magnetic field B generally acts to suppress Tc, up to some critical field strength at which Tc 0 K. Here, we investigate magnetic field–induced superconductivity in high-quality specimens of the triplet superconductor candidate UTe2 in pulsed magnetic fields up to B = 70 T. Strikingly, we find that this material has a higher Tc when B> 40 T (Tc 2.4 K) than it does for B= 0 T (Tc= 2.1 K). This observation points to a fundamentally distinct mechanism for the formation of superconductivity at high B in UTe2 compared to the case of B = 0 T.

Keywords: triplet superconductor, high magnetic field, heavy fermion


The heavy fermion paramagnet UTe2 exhibits numerous signatures of odd-parity (spin-triplet) superconductive pairing. These include high upper critical field strengths in excess of the Pauli pair-breaking limit for all orientations of B, along with only small changes in the NMR Knight shift upon crossing Tc (1, 2). Initial investigations of the superconductive properties of UTe2 studied samples grown by the chemical vapor transport technique with typical values of Tc 1.6 K (3); subsequent optimization of a salt-flux growth technique has yielded higher quality specimens with Tc = 2.1 K (4, 5). Remarkably, under the application of large magnetic fields, UTe2 exhibits two field-induced superconductive states (6). Thermodynamic evidence suggests that these phases are distinct from the ground state superconductivity found at B= 0 T (7, 8). The three superconductive phases of UTe2 are typically referred to as SC1, SC2, and SC3. The highest field superconducting state (SC3) has been found to persist up to B 70 T (9) and is acutely sensitive to the orientation of B. SC3 has been found to demonstrate a remarkable resilience against the introduction of crystalline disorder (10). Recent measurements have pointed toward the presence of quantum critical fluctuations at very high B as a likely explanation for this exotic superconductivity (11), reminiscent of the case of the ferromagnetic superconductor URhGe (12).

Results and Discussion

Here, we investigate the sensitivity to temperature and magnetic field tilt angle of the high-B SC3 superconducting phase in pristine quality UTe2. We performed contacted and contactless electrical conductivity measurements (Materials and Methods) in steady and pulsed magnetic fields, up to a maximal value of B= 70 T. Measurements were performed at magnetic field tilt angles θbc, defined as the angle of rotation from the crystallographic b axis toward the c axis.

We find that the maximal value of TcSC3 is reached for θbc 35°. In Fig. 1A we plot contactless conductivity measurements at this orientation of B for incremental temperatures. The transition to the SC3 phase is identified by a sharp dip in the derivative of the signal. This dip is still clearly visible at T= 2.3 K but is gone at T = 2.5 K. By plotting the extent of SC3 in B and T in Fig. 1C, the dashed line extrapolates to indicate TcSC3 2.4 K for this orientation of B. This is remarkable, given that for B = 0 T, TcSC1 = 2.1 K (Fig. 1D).

Fig. 1.

Fig. 1.

Enhancement of TcSC3 above TcSC1. (A) Pulsed field contactless conductivity measurements by the PDO technique (Materials and Methods) at incremental temperatures as indicated. The pronounced jump in the PDO signal at B 45 T is due to a sudden increase in resistivity upon entering the polarized paramagnetic (PPM) state at the two highest measured temperatures, and due to the sudden onset of zero resistivity at all other (lower) temperatures as the SC3 state is accessed. (B) Derivatives with respect to B of the data from panel (A). (C) The phase diagram of SC1 and SC3 for θbc= 35°, using the data from panel (A) to define the SC3 region. Note that the SC2 phase is not present at this tilt orientation of B(5). Dashed lines are given as a guide to the eye. Points for the termination of SC3 are taken from the arrows in panel (B) and plotted as “down” triangles, while “up” triangles are from the sharp onset of SC3 located at B 45 T for each of these temperatures. The extrapolation indicates that TcSC3 2.4 K for this orientation of B. (D) Contacted resistivity measurement at B = 0 T showing that TcSC1= 2.1 K. (E) The dome-like angular profile of TcSC3 plotted as a function of metamagnetic transition field BM for rotations in the bc plane, in which BM evolves as 1/cosθbc (9). Triangular points are from contacted transport in steady fields, with circular symbols from contactless conductivity measurements in pulsed fields.

We mapped the extent of SC3 at multiple orientations of B from θbc= 21° up to θbc= 46° (Fig. 2). We find that TcSC3 exhibits a dome-like angular dependence, being only 0.6 K at θbc= 21°, extending up to 2.4 K at θbc= 35°, and then reducing down to 1.8 K at θbc= 39°. For θbc 45° we find that the SC3 transition is no longer observable at 0.7 K, setting the upper boundary of the 0.7 K isotherm in Fig. 2E. We note that all temperatures quoted for pulsed field measurements were determined immediately before the pulse. These temperature values are therefore lower bounds on the actual temperature of the sample during the measurement, which may undergo some heating from eddy currents and vortex motion caused by the rapid rate of change of B.

Fig. 2.

Fig. 2.

Angular evolution of TcSC3. (A) Contacted resistivity data measured in static fields showing that at θbc= 21°, TcSC3 0.6 K. The sharp upturn in ρ is characteristic of accessing the PPM state (in the absence of coexisting superconductivity). (B) Pulsed field contactless conductivity data showing that at θbc= 32°TcSC3 2.2 K while (C) at θbc= 39°, TcSC3 1.8 K. (D) Isothermal rotation data showing the termination of SC3 for θbc 40° at T 1.5 K. (E) Angular phase diagram of UTe2 at high B, showing the temperature evolution of SC3 in the bc rotational plane. The polarized paramagnetic (PPM) and SC2 phases are also indicated, with points from ref. 5. Isotherm curves indicating the temperature domain of SC3 are drawn as guides to the eye, with quoted temperatures accurate to within approximately 0.1 K. The 0.4 K isotherm is constrained by measurements in steady fields at low θbc, and extrapolated from the angular evolution of TcSC3 observed at higher T in our pulsed field experiments at high θbc, which we include for illustrative purposes. The evolution of TcSC3 with θbc appears to be reasonably symmetric either side of θbc = 35°.

The observation of superconducting critical temperature being elevated by the application of a magnetic field is highly unusual. In the case of the related material URhGe, the observation of Tc(B=0 T)<Tc(B>0 T) was associated with the proximity to a B-induced quantum critical end point (12) located at B 10 T. What is remarkable about the case of UTe2 is that the high-B superconductivity extends up to B 70 T (9). Preliminary experiments indicate that a similar mechanism of quantum criticality driving B-induced superconductivity appears to also be at play in UTe2 (11).

Materials and Methods

UTe2 single crystals were grown in a salt flux (4) using the methodology detailed in ref. 13. Samples were screened for quality by a combination of residual resistivity, magnetic susceptibility, and specific heat capacity measurements. High-quality specimens were then oriented by X-ray Laue diffractometry.

Contacted electrical conductivity measurements were performed by the four-probe technique, with ac current sourced along the a direction at low frequencies (<50 Hz). Contactless conductivity was measured by the proximity detector oscillator (PDO) method, by the same methodology as our previous measurements reported in ref. 14. This involves tracking the change in frequency of the PDO circuitry, ΔfPDO, which relates to changes in the skin depth, resistivity, and susceptibility of the sample (15). All PDO data presented in this study were acquired on down-sweeps of magnetic field pulses, which possess a much more gradual rate of change of magnetic field strength with respect to time than the up-sweeps. Data from Hochfeldlabor-Dresden (HLD) were acquired on the same sample utilizing an identical experimental setup (but different angular orientation with respect to B) as that reported in our prior quantum interference study (14), where the excellent Lifshitz–Kosevich fitting of oscillatory amplitudes with respect to temperature gives strong confidence that the sample temperature remained close to equilibrium during the down-sweep of the magnetic field pulse.

Acknowledgments

This project was supported by the Engineering and Physical Sciences Research Council (EPSRC) of the United Kingdom (grant no. EP/X011992/1). A portion of this work was performed at the National High Magnetic Field Laboratory, which is supported by NSF Cooperative Agreement No. DMR-2128556 and the State of Florida. We acknowledge support of the Hochfeld-Magnetlabor Dresden (HLD) at Helmholtz Zentrum Dresden Rossendorf (HZDR), a member of the European Magnetic Field Laboratory (EMFL). Crystal growth and characterization were performed in the Materials Growth and Measurement Laboratory, Charles University, Prague (https://mgml.eu/), which is supported within the program of Czech Research Infrastructures (project no. LM2023065). We acknowledge financial support by the Czech Science Foundation, project No. 22-22322S. T.I.W. acknowledges support from EPSRC studentship EP/R513180/1. T.I.W. and A.G.E. acknowledge support from QuantEmX grants from Institute for Complex Adaptive Matter (ICAM) and the Gordon and Betty Moore Foundation through Grants GBMF5305 and GBMF9616 and from the US NSF Grant Number 2201516 under the Accelnet program of Office of International Science and Engineering. D.V.C. acknowledges financial support from the National High Magnetic Field Laboratory through a Dirac Fellowship, which is funded by the NSF (Grant No. DMR-1644779) and the State of Florida. A.G.E. acknowledges support from the Henry Royce Institute for Advanced Materials through the Equipment Access Scheme enabling access to the Advanced Materials Characterisation Suite at Cambridge, grant numbers EP/P024947/1, EP/M000524/1, and EP/R00661X/1; and from Sidney Sussex College (University of Cambridge).

Author contributions

V.S., M.V., F.M.G., and A.G.E. designed research; Z.W., H.C., T.I.W., A.C., D.E.G., Y.S., W.X., Y.L., Z.Z., M.V., and A.G.E. performed research; Z.W. analyzed data; and A.G.E. wrote the paper.

Competing interests

The authors declare no competing interest.

Data, Materials, and Software Availability

The datasets supporting the findings of this study are available from the University of Cambridge Apollo Repository (16).

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The datasets supporting the findings of this study are available from the University of Cambridge Apollo Repository (16).


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