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Re1−xMox as an ideal test case of time-reversal symmetry breaking in unconventional superconductors

Oct 30, 2020

Abstract Non-centrosymmetric superconductors (NCSCs) are promising candidates in the search for unconventional and topological superconductivity. The α-Mn-type rhenium-based alloys represent excellent examples of NCSCs, where spontaneous magnetic fields, peculiar to time-reversal symmetry (TRS) breaking, have been shown to develop in the superconducting phase. By converse, TRS is preserved in many other isostructural NCSCs, thus leaving the key question about its origin fully open. Here, we consider the superconducting Re1−xMox (0 ≤ x ≤ 1) family, which comprises both centro- and non-centrosymmetric structures and includes also two extra superconducting phases, β-CrFe and bcc-W. Muon-spin relaxation and rotation (μSR) measurements show a gradual increase of the relaxation rate below Tc, yet its independence of the crystal structure, suggesting that rhenium presence and its amount are among the key factors for the appearance and the extent of TRS breaking in the α-Mn-type NCSCs. The reported results propose Re1−xMox as an ideal test case for investigating TRS breaking in unconventional superconductors. Introduction Superconductors with a centrosymmetric crystal structure can host spin-singlet- or spin-triplet states with a well-defined parity—even and odd, respectively. However, in non-centrosymmetric superconductors (NCSCs), these strict symmetry-imposed requirements are relaxed, thus implying the possibility of parity-mixed superconducting states. The recent interest in NCSCs is mostly related to their unconventional superconducting properties 1 . Because of the mixed superconducting pairing, NCSCs may display significantly different properties compared to their centrosymmetric counterparts, e.g., upper critical fields beyond the Pauli limit, nodes in the superconducting gaps, etc. 1 . Owing to the possibility of mixed singlet- and triplet pairings, NCSCs rank among the foremost categories of superconducting materials in which to look for topological superconductivity or to realize the Majorana fermions, offering potential applications as, for instance, quantum computing 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 . More intriguingly, some of the NCSCs also exhibit broken time-reversal symmetry (TRS) in the superconducting state 10 , a manifestation of unconventional superconductivity. Among these, α-Mn-type ReTM (TM = Ti, Nb, Zr, and Hf) alloys represent one of the most interesting NCSC families. Widely studied by means of micro- and macroscopic techniques, they often break the time-reversal symmetry in the superconducting state 11 , 12 , 13 , 14 . A similar feature has also been discovered in centrosymmetric Sr2RuO4, PrOs4Sb12, and in pure rhenium 14 , 15 , 16 . Yet, TRS seems to be preserved in Mg10Ir19B16, Nb0.5Os0.5, and Re3W 17 , 18 , 19 . Since the latter three share the same α-Mn non-centrosymmetric structure with ReTM, this raises a very interesting fundamental question about the role of non-centrosymmetric structure in the appearance of TRS breaking in ReTM alloys. The best way to address this question consists in finding a family of compounds which exhibit crystal structures both with and without inversion symmetry, while still preserving the original stoichiometry. Indeed, despite the plausibility of the above examples, they still refer to different materials (although some of them share similar structures). Depending on the synthesis protocol, Re3W can adopt either an hcp-Mg-type (centrosymmetric) or an α-Mn-type (non-centrosymmetric) crystal structure, yet neither is found to break TRS below Tc 19 . On the other hand, many superconducting ReTM alloys, although known to break TRS, invariably adopt a single (α-Mn-type) structure 11 , 12 , 13 , 14 . In general, most ReTM phase diagrams are rather simple, with the superconducting cases being limited to the hcp-Mg- and α-Mn crystal structures. Clearly, the absence of an ideal test system leaves open the question of the origin of TRS breaking in the ReTM family and of its possible indirect link with the lack of space-inversion symmetry. Unlike the above cases, the Re1−xMox binary alloys reported here might represent such an ideal and rare candidate system. Indeed, depending on the synthesis protocol, compounds with different Re/Mo ratios can be either centrosymmetric or non-centrosymmetric while, most importantly, they all exhibit a superconducting state at low temperature 20 . In general, since the Re1−xMox system remains largely unexplored at a deeper level, we conducted systematic microscopic investigations of its superconductivity via the muon-spin relaxation and rotation (μSR) method. This required the synthesis and the preliminary characterization of the magnetic, electrical, and thermodynamic properties of the full range of Re1−xMox solid solution 20 . The μSR results presented here allow us not only to establish the presence of TRS breaking but also to quantify it. By correlating the extent of TRS breaking in the Re1−xMox series to the Re-content we find that in ReTM materials the time-reversal symmetry breaking is most likely related to the Re content rather than to crystal structure. Results Rich structural- and superconducting phase diagram According to diffraction- and physical-properties characterizations, binary Re1−xMox alloys exhibit very rich structural- and superconducting phase diagrams. As shown in Fig. 1 a, depending on Re/Mo concentration, different synthesis procedures can produce four different solid phases: hexagonal hcp-Mg (P63/mmc, No. 194), cubic α-Mn ($$I\overline{4}3m$$, No. 217), tetragonal β-CrFe (P42/mnm, No. 136), and cubic bcc-W ($$Im\overline{3}m$$, No. 229). Except for the non-centrosymmetric α-Mn, the other three structures are centrosymmetric. Their unit-cell crystal structures are shown schematically in Fig. 1 b, while details such as the lattice parameters and the atomic coordinates are reported elsewhere 20 . Although Re1−xMox alloys exhibit different crystal structures as x changes, they all become superconductors at low temperature. By increasing the Mo content, the superconducting transition temperature Tc varies non-monotonically, thus defining three distinct superconducting regions. The first superconducting region (achieved on the Re-rich side and with highest Tc = 9.43 K), corresponds to alloys adopting an hcp-Mg-type structure. For x = 0.23, both centrosymmetric (hcp-Mg) and non-centrosymmetric (α-Mn) crystal structures are obtained, the latter showing a Tc value about 1 K lower than the former. In the second superconducting region, where the alloys adopt a β-CrFe-type structure, the superconducting transition temperature Tc ~ 6.3 K is somewhat lower than in the other regions and almost independent of Mo content. Upon further increasing the Mo content, the third superconducting region shows up for x > 0.5. Here, all the samples display a cubic bcc-W-type structure and the highest Tc reaches 12.4 K (for x = 0.6). Close to the phase boundaries, the alloys show multiple superconducting transitions. To exclude possible extrinsic effects related to them, the μSR measurements were performed only on samples away from the phase boundaries. Fig. 1: Structural and superconducting phase diagram of Re1−xMox. a The phase diagram of the binary Re1−xMox alloys includes four different solid phases, whose crystal structures are shown schematically in b. For x = 0.23, both centrosymmetric (hexagonal hcp-Mg) and non-centrosymmetric (cubic α-Mn) structures can be obtained. The details of the crystal structures can be found in Shang et al. 20 . b Superconducting transition temperatures Tc versus Mo content, as determined from electrical resistivity, magnetic susceptibility, and specific-heat measurements (see ref. 20 ). Colors identify the various phases and highlight the correlation between the superconducting properties and crystal structures. Discussion First, we discuss why ReTM are fully-gapped superconductors. The lack of inversion symmetry in NCSCs often induces an antisymmetric spin-orbit coupling (ASOC), which splits the Fermi surface by lifting the degeneracy of the conduction-band electrons. As a consequence, both inter- and intraband Cooper pairs with the same or with opposite spin directions can be formed, thus allowing admixtures of spin-triplet and spin-singlet SC pairing. In general, the degree of such admixture is determined by the strength of ASOC and other microscopic parameters 1 , 10 . Yet, normally it is the ASOC to play the key role in the superconducting properties of NCSCs 1 . By increasing the strength of ASOC, a fully-gapped superconductor can be tuned into a nodal superconductor, the latter typically being dominated by the spin-triplet SC pairing. Such mechanism has been shown to occur, e.g., in Li2(Pd,Pt)3B 28 , 29 and, more recently, in CaPtAs 26 , 30 . As for ReTM NCSCs, despite the relatively large ASOC of rhenium atoms, all of them exhibit fully-gapped superconducting states, more consistent with singlet pairing 11 , 12 , 13 , 14 , 19 , 27 . However, we recall that often, due to the similar magnitude and same-sign of the order parameter on the spin-split Fermi surfaces, a possible mixed-pairing superconductor may be challenging to observe or to distinguish from a single-gap s-wave superconductor 31 . Considering that ReTM superconductors frequently exhibit TRS breaking below Tc, the existence of triplet pairing (and nodal superconductivity) is to be expected. For instance, both triplet-pairing and TRS breaking superconductivity have been reported in Sr2RuO4, UPt3, LaNiGa2, and LaNiC2 15 , 22 , 24 , 32 , 33 , 34 , the latter representing a typical NCSC. In the α-Mn-type ReTM alloys, close to the Fermi level, the density of states (DOS) is dominated by the 5d orbitals of rhenium atoms, while contributions from the d orbitals of TM are negligible 35 , 36 . Hence, even a significant increase in SOC—from 3d Ti to 4d Zr/Nb/Mo and to 5d Hf/Ta/W—is shown to not significantly affect the pairing admixture and thus the superconducting properties. Hence, in the ReTM family, the effect of ASOC on admixtures of pairing remains elusive and requires additional work. Unlike in the generic ReTM case, in the Re1−xMox series considered here, the Re and Mo atoms occupy the same atomic positions of a centrosymmetric unit cell 20 . Hence, as the Mo content increases, the contribution of Mo 4d orbitals to the DOS is progressively enhanced, at the expense of the Re 5d orbitals. Naively, one would expect a progressive increase in singlet-pairing character as the Mo content increases. Yet, according to TF-μSR (Fig. 4 ) and zero-field specific-heat results 20 , it seems that, despite a change in stoichiometry and of different crystal structures (both centro- and non-centrosymmetric) adopted by the Re1−xMox alloys, they all behave as fully-gapped superconductors. This finding strongly suggests that, in the ReTM superconductors, spin-singlet pairing is dominant. Second, we consider the role of rhenium in the time-reversal symmetry breaking. A dominating spin-singlet pairing in ReTM superconductors is clearly puzzling in view of the frequent occurrence of TRS breaking in this class of superconductors. As discussed above, the DOS is mostly determined by the Re 5d orbitals, since a replacement on the T-sites appears to have negligible effects on TRS breaking and on the superconducting pairing. At the same time, TRS is preserved in other Re-free α-Mn-type superconductors with similar SOC strength, as e.g., binary Nb0.5Os0.5 and ternary Mg10Ir19B16 17 , 18 , 37 . The marginal role of SOC, together with the observation of broken TRS also in centrosymmetric elemental rhenium, strongly suggests that rhenium is crucial for understanding the broken TRS in the ReTM superconductors 14 . Considering that pure rhenium has a centrosymmetric crystal structure, the non-centrosymmetric crystal structure seems also inessential to TRS breaking in α-Mn-type Re-based superconductors. These indirect conclusions are clearly confirmed by our ZF-μSR measurements on Re1−xMox (0 ≤ x ≤ 0.60) across the whole structural phase diagram. The measurements we report here serve a dual purpose. Firstly, we extend previous σZF(T) results on elemental Re down to 0.02 K (originally limited to 1.5 K, although the Tc of Re is only 2.7 K). The current data (see Fig. 2 c) are highly consistent with the previous ones 14 and exhibit a clear increase of σZF(T) near Tc, thus confirming that elemental rhenium breaks TRS in its superconducting state. Secondly, by systematically investigating the four different solid phases of Re1−xMox (0 ≤ x ≤ 0.60) via ZF-μSR, we find that only those compounds close to the Re-rich side (x ≤ 0.12, including elemental Re) show a superconducting state with broken TRS. In fact, for x > 0.12, although Re1−xMox alloys exhibit various crystal structures (including the non-centrosymmetric α-Mn type), the TRS is preserved in the superconducting state, again implying that TRS breaking is not related to the lack of a center of symmetry, but rather to the presence of rhenium and to its content. Such conclusion is further reinforced by the preserved TRS in the extremely diluted Re-based superconductor, ReBe22, whose Re-content is only 4% 38 . Finally, we discuss the relationship between TRS breaking and superconducting pairing. In general, this is a complex and still open question. Unconventional pairings, such as spin-triplet, are expected to break TRS in the superconducting state. For instance, Sr2RuO4 and UPt3 exhibit both triplet superconductivity and broken TRS 39 , 40 , 41 , 42 , the latter having been confirmed by ZF-μSR and Kerr effect 15 , 24 , 32 , 33 . Conversely, there are broken TRS states not involving triplet pairing, as e.g., the s + id spin-singlet state proposed for some iron-based high-Tc superconducting materials 43 . In case of weak SOC, the internally-antisymmetric nonunitary triplet (INT) pairing can break the TRS, e.g., in centrosymmetric LaNiGa2 34 , 44 , 45 , and non-centrosymmetric LaNiC2 22 , 46 . For such INT, the superconducting paring function is antisymmetric with respect to the orbital degree of freedom, while remaining symmetric in the spin- and crystal-momentum channels 22 , 34 , 44 , 46 . In Re-based superconductors, the point groups Td and D6h, relevant to α-Mn-type ReTM and hcp-Mg-type Re and Re0.88Mo0.12, respectively, have few irreducible representations whose dimension is larger than 1. In this case, an INT state can be achieved also in ReTM superconductors, where it can account for broken TRS in presence of a fully-opened gap, with either singlet-, triplet-, or admixed pairing. We recall that in ReTM superconductors, neither the TRS breaking nor the fully-gapped superconducting states are closely related to the structure symmetry, thus indicating that SOC is here inessential. Since SOC is ignored in INT pairing, this paradigm could provide a simple explanation of why a lack of inversion symmetry (essential to SOC) is not a precondition for TRS breaking in ReTM superconductors. Moreover, the occurrence of an INT state relies on the availability of a local-pairing mechanism driven by Hund’s rules, e.g., by Ni d-electrons in LaNiC2 and LaNiGa2 22 , 34 , 44 , 45 , 46 . Since rhenium, too, can induce magnetism 47 , 48 , such local-pairing mechanism may occur also in ReTM superconductors. In the latter case, TRS breaking would depend on Re content but not on crystal structure, in agreement with the results we report here. To conclude, in search of the origin of time-reversal symmetry breaking in Re-based superconductors, we performed comparative μSR studies in the Re1−xMox family, covering all its four different solid phases: hcp-Mg, α-Mn, β-CrFe, and bcc-W, with α-Mn being non-centrosymmetric and the other three centrosymmetric. The superconductivity of Re1−xMox, including the lower and upper critical fields, was characterized by magnetization, electrical resistivity, and heat capacity measurements. The superfluid density at a microscopic level and the zero-field electronic specific heat at a macroscopic level both reveal a fully-gapped superconductivity in Re1−xMox. The spontaneous fields increase with decreasing temperature (below the onset of superconductivity), indicating that the superconducting states of centrosymmetric Re and Re0.88Mo0.12 break the TRS and are unconventional. By contrast, TRS is preserved in the Re1−xMox compounds with a lower Recontent (i.e., x ≥ 0.23), independent of their centro- or non-centrosymmetric crystal structures. Our findings on the Re1−xMox family (here extended to two other superconducting phases, β-CrFe and bcc-W), together with those regarding other Re-free α-Mn-type superconductors, clearly imply that not only the Re presence, but also its amount are crucial for the appearance and the extent of TRS breaking in the ReTM superconductors. Further theoretical and experimental work is highly desirable to clarify the rhenium conundrum. Methods Sample preparation Polycrystalline Re1−xMox alloys were prepared by arc melting Re (99.99%, ChemPUR) and Mo (99.95%, ChemPUR) powders with different stoichiometric ratios in a high-purity argon atmosphere. To improve the homogeneity, samples were flipped and remelted several times and, some of the as-cast ingots, e.g., hcp-Mg- and bcc-W-type, were annealed at 900∘C for two weeks. The clean β-CrFe phase (e.g., Re0.55Mo0.45) was obtained by interrupting the heating immediately after the melting of the precursors, similar to a quench process. Hence, all the measurements reported here for the β-CrFe-type samples refer to as-cast samples. The α-Mn-type samples with a non-centrosymmetric crystal structure (e.g, Re0.77Mo0.23) were synthesized by both arc melting and solid-state reaction methods. The arc-melted sample, which shows a majority of hcp-Mg phase, was annealed over one week at 1400 ∘C in a mixed argon/hydrogen (95%/5%) atmosphere to stabilize the α-Mn phase. Such phase could also be obtained by annealing the mixture of Re and Mo powders at 1400 ∘C in argon/hydrogen atmosphere over one week. Lower- and upper critical fields The lower critical field Hc1 was determined by field-dependent magnetization measurements at various temperatures up to Tc, while the upper critical field Hc2 was determined by measuring the temperature-dependent electrical resistivity and heat capacity under various magnetic fields, and by field-dependent magnetization at various temperatures. The magnetization, electrical resistivity, and heat capacity measurements were performed on a Quantum Design magnetic property measurement system (MPMS) and a physical property measurement system (PPMS). The details of zero-field electrical resistivity and heat capacity results, as well as the low-field magnetic susceptibility data are reported in a previous study (see Shang et al. 20 ). The results of the lower critical field measurements for Re1−xMox (0.12 ≤ x ≤ 0.60) are summarized in Supplementary Fig. 3 . The estimated μ0Hc1(0) values are listed in the right panel of Supplementary Fig. 3 and in Supplementary Table 1 . The μ0Hc1(0) of pure Re (hcp-Mg) can be found in Shang et al. 14 . The results of the upper critical fields Hc2 for Re1−xMox (0 ≤ x ≤ 0.60) are presented in Supplementary Figs. 7 , 9 . The μ0Hc2(T) data were analyzed by both Werthamer–Helfand–Hohenberg (WHH) and Ginzburg–Landau (GL) models 49 , 50 . The estimated μ0Hc2(0) values are also listed in Supplementary Table 1 . The coherence length ξ(0) was calculated from ξ(0) = $$\sqrt{{\Phi }_{0}/2\pi \ {H}_{{\rm{c2}}}(0)}$$, where Φ0 = 2.07 × 10−3 T μm2 is the quantum of magnetic flux. The GL magnetic penetration depth λGL is related to the coherence length and the lower critical field via μ0Hc1 = ($${\Phi }_{0}/4\pi {\lambda }_{{\rm{GL}}}^{2}$$)[$$\mathrm{ln}\,(\kappa )+0.5$$], where κ = λGL/ξ is the GL parameter 51 . By using μ0Hc1(0) and ξ(0) calculated from μ0Hc2(0), the GL magnetic penetration depths λGL(0) could be determined. They too are listed in Supplementary Table. 1 and are fully consistent with the experimental values from TF-μSR data. The GL parameter κ for Re1−xMox (0 ≤ x ≤ 0.60) (see Supplementary Table 1 ), is always much larger than the threshold value $$1/\sqrt{2}$$, thus clearly confirming that all Re1−xMox alloys are type-II superconductors. μSR experiments The μSR experiments were conducted at the general-purpose surface-muon (GPS) and at the low-temperature facility (LTF) instruments of the Swiss muon source (SμS) at Paul Scherrer Institut (PSI) in Villigen, Switzerland. Once implanted in a material, typically within ~0.1 mm, spin-polarized muons act as microscopic probes of the local magnetic environment via the decay positrons, emitted preferentially along the muon-spin direction. The spatial anisotropy of the emitted positrons (i.e., the asymmetry signal) reveals the distribution of the local magnetic fields at the muon stopping sites. For ZF-μSR measurements, to exclude the possibility of stray magnetic fields, the magnets were quenched before starting the measurements, and an active field-nulling facility was used to compensate for stray fields down to 1 μT. In both the TF- and LF-μSR cases, the samples were cooled in an applied magnetic field down to the base temperature (1.5 K for GPS and 0.02 K for LTF). The μSR spectra were then collected upon heating. Analysis of the ZF-μSR data All the μSR data were analyzed by means of the musrfit software package 52 . Due to the non-magnetic nature of Re1−xMox, in the absence of applied external fields, the relaxation is mainly determined by the randomly oriented nuclear moments. Therefore, the ZF-μSR spectra can be modeled by means of a phenomenological relaxation function, consisting of a combination of Gaussian- and Lorentzian Kubo-Toyabe relaxations 53 , 54 : $${A}_{{\rm{ZF}}}={A}_{{\rm{s}}}\left[\frac{1}{3}+\frac{2}{3}(1-{\sigma }_{{\rm{ZF}}}^{2}{t}^{2}-{\Lambda }_{{\rm{ZF}}}t)\ {{\rm{e}}}^{\left(-\frac{{\sigma }_{{\rm{ZF}}}^{2}{t}^{2}}{2}-{\Lambda }_{{\rm{ZF}}}t\right)}\right]+{A}_{{\rm{bg}}}.$$ (1) Here As and Abg represent the initial muon-spin asymmetries for muons implanted in the sample and the sample holder, respectively. The muon-spin polarization, reported in the top row of Fig. 2 , is the total initial asymmetry AZF normalized to its t = 0 value. In polycrystalline samples, the 1/3-non-relaxing and 2/3-relaxing components of the asymmetry correspond to the powder average of the local internal field with respect to the initial muon-spin orientation. The σZF and ΛZF represent the zero-field Gaussian and Lorentzian relaxation rates, respectively. Since ΛZF shows an almost temperature-independent behavior, the σZF values in Fig. 2 c and d could be derived by fixing ΛZF to its average value, here, ΛZF = 0.0144 (x = 0) and 0.005 μs−1 (x = 0.12). Further details about the data analysis can also be found in Shang et al. 14 . Analysis of the TF-μSR data In the TF-μSR case, the time evolution of the asymmetry can be modeled by: $${A}_{{\rm{TF}}}(t)=\mathop{\sum }\limits_{{\rm{i=1}}}^{{\rm{n}}}{A}_{{\rm{i}}}\cos ({\gamma }_{\mu }{B}_{{\rm{i}}}t+\phi ){e}^{-{\sigma }_{{\rm{i}}}^{2}{t}^{2}/2}+{A}_{{\rm{bg}}}\cos ({\gamma }_{\mu }{B}_{{\rm{bg}}}t+\phi ).$$ (2) Here Ai and Abg are the same as in ZF-μSR. Bi and Bbg are the local fields sensed by implanted muons in the sample and the sample holder, γμ is the muon gyromagnetic ratio, ϕ is the shared initial phase, and σi is the Gaussian relaxation rate of the ith component. The number of the required components depends on the field distribution in the mixed superconducting state, here we found 1 ≤ n ≤ 3 for Re1−xMox. In case of multi-component oscillations, the first term in Eq. ( 2 ) describes the field distribution as the sum of n Gaussian relaxations 55 : $$p(B)={\gamma }_{\mu }\mathop{\sum }\limits_{{\rm{i=1}}}^{{\rm{n}}}\frac{{A}_{{\rm{i}}}}{{\sigma }_{{\rm{i}}}}\exp \left(-\frac{{\gamma }_{\mu }^{2}{(B-{B}_{{\rm{i}}})}^{2}}{2{\sigma }_{{\rm{i}}}^{2}}\right).$$ (3) The first- and the second moments of the field distribution in the sample can be calculated by: $$\langle B\rangle =\mathop{\sum }\limits_{{\rm{i=1}}}^{{\rm{n}}}\frac{{A}_{{\rm{i}}}{B}_{{\rm{i}}}}{{A}_{{\rm{tot}}}},$$ (4) and $$\langle {B}^{2}\rangle =\frac{{\sigma }_{{\rm{eff}}}^{2}}{{\gamma }_{\mu }^{2}}=\mathop{\sum }\limits_{{\rm{i=1}}}^{{\rm{n}}}\frac{{A}_{{\rm{i}}}}{{A}_{{\rm{tot}}}}\left[\frac{{\sigma }_{{\rm{i}}}^{2}}{{\gamma }_{\mu }^{2}}+{({B}_{{\rm{i}}}-\langle B\rangle )}^{2}\right],$$ (5) where $${A}_{{\rm{tot}}}=\mathop{\sum }\nolimits_{{\rm{i = 1}}}^{{\rm{n}}}{A}_{{\rm{i}}}$$. The total Gaussian relaxation rate σeff in Eq. ( 5 ) includes contributions from both a temperature-independent relaxation, due to nuclear moments (σn, similar to σZF), and a temperature-dependent relaxation, related to the flux-line lattice (σsc) in the superconducting state. The σsc values were extracted by subtracting the nuclear contribution following σsc = $$\sqrt{{\sigma }_{{\rm{eff}}}^{2}-{\sigma }_{{\rm{n}}}^{2}}$$. Extracting the superconducting gap and its symmetry from TF-μSR data Since σsc is directly related to the effective magnetic penetration depth and thus to the superfluid density ($${\sigma }_{{\rm{sc}}}\propto 1/{\lambda }_{{\rm{eff}}}^{2} \sim {\rho }_{{\rm{sc}}}$$), the superconducting gap and its symmetry can be investigated by measuring the temperature-dependent σsc. For small applied magnetic fields [Happl/Hc2 ≪ 1], the effective magnetic penetration depth λeff can be calculated from the measured σsc 51 , 56 : $$\frac{{\sigma }_{{\rm{sc}}}^{2}(T)}{{\gamma }_{\mu }^{2}}=0.00371\ \frac{{\Phi }_{0}^{2}}{{\lambda }_{{\rm{eff}}}^{4}(T)}.$$ (6) For Re1−xMox (0 ≤ x ≤ 0.60), the Happl/Hc2 ratios are comprised between 0.23% and 2.6% (see Supplementary Table 1 ), hence justifying the use of the above equation. To extract the superconducting gap and its symmetry, the temperature-dependent superfluid density ρsc(T) [$$\propto {\lambda }_{{\rm{eff}}}^{-2}(T)$$] of Re1−xMox was analyzed by using a fully gapped s-wave model, generally described by: $${\rho }_{{\rm{sc}}}(T)=\frac{{\lambda }_{0}^{2}}{{\lambda }_{{\rm{eff}}}^{2}(T)}=1+2\mathop{\int}\nolimits_{\Delta (T)}^{\infty }\frac{E}{\sqrt{{E}^{2}-{\Delta }^{2}(T)}}\frac{\partial f}{\partial E}{\rm{d}}E,$$ (7) where $$f={(1+{e}^{E/{k}_{{\rm{B}}}T})}^{-1}$$ is the Fermi function 57 , 58 , λ0 is the effective magnetic penetration depth at zero temperature. The temperature dependence of the gap value is given by $$\Delta (T)={\Delta }_{0}\tanh \{1.82{[1.018({T}_{{\rm{c}}}/T-1)]}^{0.51}\}$$ 59 , where Δ0 is the gap value at zero temperature. Unlike in the clean-limit case [see Eq. ( 7 )], in the dirty limit, the coherence length ξ0 is larger than the electronic mean-free path le. In this case, in the BCS approximation, the temperature dependence of the superfluid density is given by 57 : $${\rho }_{{\rm{sc}}}(T)=\frac{{\lambda }_{0}^{2}}{{\lambda }_{{\rm{eff}}}^{2}(T)}=\frac{\Delta (T)}{{\Delta }_{0}}\tanh \left[\frac{\Delta (T)}{2{k}_{{\rm{B}}}T}\right].$$ (8) For Re1−xMox (0 ≤ x ≤ 0.60), ξ0 and le exhibit similar magnitudes. Hence, in this case, both Eqs. ( 7 ) and ( 8 ) describe very well the low-T superfluid density, and yield similar superconducting gap values (see Supplementary Table 1 ). Data availability All the data needed to evaluate the reported conclusions are presented in the paper and/or in the Supplementary Materials. Additional data related to this paper may be requested from the authors. The μSR data were generated at the SμS (Paul Scherrer Institut, Switzerland). Derived data supporting the results of this study are available from the corresponding authors or beamline scientists. 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