We report a study on tuning the charge density wave (CDW) ferromagnet SmNiC2 to a weakly coupled superconductor by substituting La for Sm. X-ray diffraction measurements show that the doped compounds obey Vegard’s law, where La (Lu) alloying expands (shrinks) the lattice due to its larger (smaller) atomic size than Sm. In the series Sm1−xLaxNiC2, CDW transition (TCDW = 148 K) for SmNiC2 is gradually suppressed, while the ferromagnetic (FM) ordering temperature (TC) at 17 K slightly increases up to x = 0.3. For x > 0.3, TC starts to decrease and there is no signature that could be related with the CDW phase. Electrical resistivity, magnetic susceptibility and specific heat measurements point toward the possible presence of a FM quantum critical point (QCP) near x = 0.92, where the TC is extrapolated to zero temperature. Superconductivity in LaNiC2 (Tsc = 2.9 K) is completely suppressed with small amount of Sm inclusion near the proposed FM critical point, indicating a competition between the two ordered phases. The tunable lattice parameters via chemical substitution (La,Lu) and the ensuing change among the ordered phases of ferromagnetism, CDW and superconductivity underscores that SmNiC2 provides a rich avenue to study the rare example of a FM QCP, where the broken symmetries are intricately correlated.
Recently, study on a quantum critical point (QCP) has attracted great interest because of the possibility of previously unknown phases of matter from the singular quantum fluctuations associated with the QCP1. There exist a plethora of reports on antiferromagnetic (AFM) QCP systems, but examples with a ferromagnetic (FM) QCP are rare2,3,4. The CDW ferromagnet SmNiC2 shows a quasi-one-dimensional electronic structure, which leads to a CDW state from the Fermi surface nesting, e.g., Peierls instability5. Study on the effects of hydrostatic pressure in SmNiC2 has suggested that singular quantum fluctuations may create novel quantum phases in a vicinity of the projected FM quantum critical point (QCP) near 3.8 GPa (ref. 6). These novel phases, however, hide the presence of the QCP, requiring an alternative approach to probe the nature of the candidate FM QCP. Recently, Kim et al. predicted that both hydrostatic and chemical pressure have similar effects in tuning the electronic states of SmNiC2 (ref. 7).
Ternary rare-earth nickel carbides (RNiC2) were first reported by Bodak8, which are formed in an orthorhombic Amm2 (space group #38) crystal structure with Ni and the rare-earth (R) metal chains being aligned along the crystallographic a-axis. This system is of particular interest because both CDW and long range magnetic ordering phases have been observed together. Among the RNiC2 compounds only two – SmNiC2 and LaNiC2 – exhibit properties other than an AFM ground state. Magnetism in RNiC2 originates from the lanthanide sublattice and displays an AFM ordering in most cases (R = Ce, Pr, Nd, Gd, Tb, Dy, Ho, Er, Tm)9,10. The exceptions, SmNiC2 and LaNiC2, are a ferromagnet and a superconductor, respectively. We note that the crystal structure of LuNiC2 has been reported11, but to our knowledge physical properties of this compound remain unknown.
In SmNiC2, the low-temperature synchrotron x-ray diffraction reveals that a CDW state with the wave vector q = (0.5, 0.52, 0) forms below 148 K and disappears below the Curie temperature 17.7 K, indicating destruction of the CDW due to appearance of the ferromagnetic ordering12. This is different from NdNiC2 where a CDW is still observed below the Nèel temperature (in the AFM state)13. The coexistence of a CDW with superconductivity is also observed in Er5Ir4Si10 and Lu5Ir4Si10 (refs 14 and 15).
Superconductivity in the first member of RNiC2 family, LaNiC2 with Tsc = 2.9 K, was first reported by W. H. Lee, et al. almost two decades ago8. Superconducting critical temperature can be increased to 8 K in the solid solution La0.5Th0.5NiC2 (ref. 16). In contrast, Y doping of La1−xYxNiC2 decreases Tsc (ref. 17). Nuclear quadrupole relaxation (NQR)18 and specific heat19 measurements suggest that LaNiC2 is a conventional BCS superconductor. A pure singlet pairing state has been reported for the non-centrosymmetric superconductors: Li2Pd3B (ref. 20), BaPtSi3 (ref. 21), Re3W (ref. 22), Mg10Ir19B16 (ref. 23). However, strong evidences for an unconventional character of superconductivity in LaNiC2 have been recently suggested by muon spin relaxation (μSR)24,25 and penetration depth experiments26. In addition, a phenomenological two-gap BCS model was recently proposed by Kim et al.7. The uncertainty on the nature of superconductivity for LaNiC2 makes it more important to study the relationship between superconductivity and ferromagnetism.
Here we report crystallographic and physical properties of Sm1−xLaxNiC2 and Sm1−yLuyNiC2, where La and Lu were substituted for Sm to introduce negative and positive chemical pressures, respectively. X-ray diffraction study showed that the volume change in the La (or Lu) alloyed compounds obeys Vegards’ law: La (Lu) alloying expands (shrinks) the volume linearly. Since La is an element with empty 4f orbital and Lu has a fully filled 4f orbital with J = 0, the chemical alloying does not introduce magnetism to the system, but is expected to induce chemical pressure effects through a change in the distance between constituent elements. Magnetic susceptibility, electrical resistivity and heat capacity data point toward the possible presence of a FM quantum critical point near x = 0.92, where the Curie temperature TC is extrapolated to zero temperature and the specific heat divided by temperature is strongly enhanced with decreasing temperature down to the lowest measuring temperature. Comprehensive magnetic and superconducting phase diagram for both Sm1−xLayNiC2 and Sm1−yLuyNiC2 is constructed for the first time.
X-ray Diffraction Measurements
Powder XRD patterns are presented in Fig. 1(a) for Sm1−xLaxNiC2 and Sm1−yLuyNiC2. Main reflection peaks clearly shift towards lower and higher angles for Sm1−xLaxNiC2 and Sm1−yLuyNiC2, respectively. This is consistent with the larger (smaller) ionic radius of La3+ (Lu3+) than Sm3+ and confirms successful chemical alloying. The panels (b–e) of Fig. 1 present the Le Bail refinements performed using the FULLPROF diffraction suite27 for representative Sm1−xLaxNiC2 (x = 0, 0.2, 0.8 and 1.0) samples. The refinements confirm an orthorhombic Amm2 crystal structure (s.g. #38) and give the lattice parameters for Sm1−xRxNiC2 (R = La and Lu). More detailed inspection of the Sm1−xLaxNiC2 series of the XRD patterns reveals a slight broadening and splitting in the main reflection peaks for 0.2 ≤ x ≤ 0.6. An excellent Le Bail fit (Rwp = 11.7, Rexp = 8.65, χ2 = 1.84) was obtained by assuming the presence of two phases with the same crystal structure and different lattice parameters as can be seen for Sm0.8La0.2NiC2 (see Fig. 1c). This suggests that two distinct compounds Sm1−xLaxNiC2 with slightly different La concentrations (x) are present for the intermediate composition range. The majority phase is the one with smaller x – the Sm-richer variant. Such behaviour is not observed for Lu-doped series. The refined lattice parameters for Sm1−xLaxNiC2 are shown in Fig. S1 of the Supplementary Information. The a and c lattice parameters obey Vegard’s law for the whole La concentration range, while the b parameter is almost constant up to x = 0.3 and linearly increases with further increasing La level. The rigid C-C dimers along the b direction are likely responsible for the negligible change in the b lattice constant for the lower La level10. The intermediate region, in which two phases with different La/Sm ratio are present, is shadowed on the diagram and the lattice parameters for the second, minority phase are shown by triangles.
The relative change (ΔL/L0) of each lattice parameter vs. nominal concentration of La and Lu for Sm1−xLaxNiC2 and Sm1−yLuyNiC2 is presented in Fig. 2. ΔL is the change of each lattice parameter compared to the lattice parameter (L0) of the parent (SmNiC2) compound. For example Δa/a0 was calculated from (ax − a0)/a0, where ax and a0 are the a-axis lattice parameters for Sm1−xLaxNiC2 and SmNiC2, respectively. With increase in x, the lattice parameter along the a-axis expands more rapidly than that along the b- and c-axis: as large as a 7% increase in the a-axis is observed, while less than 1% change occurs along the b-axis. In contrast, Lutetium doping (y) causes a decrease of the lattice parameters, which is most pronounced along the a-axis.
Resistivity measurements were performed for Sm1−xLaxNiC2 (0 ≤ x ≤ 1) and Sm1−yLuyNiC2 (0 ≤ y ≤ 0.4) series. Temperature dependence of the normalized resistivity is shown in Fig. 3 for Sm1−xLaxNiC2, where resistivity values are normalized to those at 300 K for comparison. Depending on the La concentration, three features are observed. For the parent SmNiC2 and slightly La doped (x < 0.3) Sm1−xLaxNiC2, a sharp inflection at high temperature is seen due to a charge density wave (CDW) formation. TCDW was assigned as the minimum of the temperature derivative of resistivity (dρ/dT). For the parent compound SmNiC2 the obtained TCDW (=148 K) is comparable with the previous reports10,28. With increase in La content, the CDW transition temperature starts to decrease rapidly, reaches to 34 K for Sm0.7La0.3NiC2, and is not observed for x > 0.3. The increase in resistivity just below TCDW is due to a CDW gap opening on the Fermi surface. For SmNiC2 resistivity reaches a maximum at about 120 K and decreases with further decrease of temperature. Another feature that is clearly visible for SmNiC2 is a sharp drop in resistivity at 17.2 K (see Fig. 3(b)), which is caused by the ferromagnetic (FM) phase transition, as will be supported by magnetic measurements. Although such behaviour is typically seen for ferromagnetic compounds below the Curie temperature, one order of magnitude decrease of resistivity is rare and may originate from the destruction of the CDW state at the same temperature. When a CDW is present, ferromagnetism is robust. In fact, there is a slight increase in the Curie temperature from 17.2 K (SmNiC2) to 17.8 K (Sm0.25La0.75NiC2) with increasing x. For x > 0.3, the CDW transition is no longer observed and the Curie temperature starts to decrease with increasing La concentration, which suggests a strong correlation between the CDW and ferromagnetic phases.
Figure 3(c) presents resistivity data for Sm1−xLaxNiC2 system with high La concentration (x ≥ 0.9). A sharp superconductivity transition is observed for LaNiC2 and Sm0.02La0.98NiC2 with Tsc = 3.4 K and 2 K, respectively. The samples with slightly lower x (0.97 and 0.95) do not show a transition to the zero-resistance superconducting state above 1.8 K, suggesting that the resistivity drop is due to filamentary nature of the SC phase. The rapid suppression of superconductivity is often observed in the presence of magnetic impurities that act as strong scattering centers to destroy superconducting Cooper pairs. One such example is La1−xGdx alloy, where only 1% of Gd alloying suppresses Tsc from almost 6 K for La to 1 K for La0.99Gd0.01 (ref. 29).
In contrary to La alloying, the low-T normalized resistivity of SmNiC2 is enhanced by Lu alloying (see Fig. S2 in the Supplementary Information). The slope of the resistivity (dρ/dT) at high temperatures decreases with increase of Lu concentration, too. The 20% Lu-doped compound (Sm0.8Lu0.2NiC2) reveals both CDW and FM behaviour. The Curie temperature is suppressed to 10 K, whereas the CDW transition temperature increases to 152 K, a 4 K increase from the pure compound. It is in contrast to the La-doping (Sm1−xLaxNiC2): at the same concentration level (x = 0.2), TCDW is suppressed to 126 K, a 24 K decrease.
Magnetic characterization of the Sm1−xLaxNiC2 series is presented in Fig. 4. There are no anomalies at around 13 K and 25 K that originates from the presence of SmNi2 binary phase9. The absence of anomalous features suggests high quality of our samples. The molar magnetic susceptibility (χM) at μoH = 0.1 T (Fig. 4a) shows a rapid increase with decreasing temperature below 17 K and saturates between 0.5 to 1.2 emu/Sm mol for different La concentrations at low temperatures. At this moment, it is difficult to point out a correlation between the saturated moments and alloying concentrations because the samples are in a polycrystalline form. The FM transition temperature determined by the minimum of the temperature derivative of susceptibility (dχ/dT), as shown in Fig. 4b, is in good agreement with the Curie temperature TC = 17.2 K from the resistivity measurement. Ferromagnetism in Sm1−xLaxNiC2 is robust. TC initially increases with La concentration, reaches a maximum of 18 K at x = 0.25, and then decreases with further increasing La level, showing a small dome shape in the T-x phase diagram. It is interesting to note that the ferromagnetic phase persists up to the nominal La concentration x = 0.86: a ferromagnetic transition at as low as 2.5 K was observed for the composition x = 0.86 in the series Sm1−xLaxNiC2. In order to confirm the ferromagnetic state and precisely estimate the Curie temperature, the Arrott plot analysis was performed. A series of isothermal magnetisation curves in the immediate vicinity of the Curie temperature were measured. In a plot of H/M vs M2, the isotherm which passes through the origin gives the best estimate of Curie temperature because H/M = βM2 at T = TC (ref. 30). The Arrott plot presented in Fig. 5 shows that the ferromagnetic transition temperature for Sm0.2La0.8NiC2 is 5.5 K, very close to TC = 5.3 K estimated for the same sample from the minimum of dχ/dT. Using the Arrott plot, TC = 3.5 K was estimated for Sm0.14La0.86NiC2 (not shown here).
A molar magnetic susceptibility at 300 K for the Sm1−xLaxNiC2 series is shown in Fig. S3 of the Supplementary Information, which linearly decreases with increasing La concentration. As expected, the extrapolated line reaches zero at LaNiC2. The same experimental data normalized per Sm-mol is almost independent of x and is about χ(300K) = 1.8 × 10−3emu/Sm-mol, indicating that La is successfully substituted for Sm.
According to H. Onodera et al., spontaneous magnetization (M) along the a-axis of the single crystal (~0.32 μB) is smaller than 0.72 μB for Sm3+, while it is negligible along the b- and c-axis9. The fact that we have obtained 0.19 μB at 2 K could be ascribed to the polycrystalline form of the measured sample. Such a small value has been explained by the mixed valence state of Sm2+ and Sm3+ ions or crystalline electric field (CEF) effects. A mixed valent state is common in Sm containing compounds. Above the ferromagnetic transition temperature the entire series did not follow the Curie-Weiss behaviour, which might be pertinent to the mixed valent state of Sm ions. It is imperative to study the exact nature of magnetic interactions present in SmNiC2 by measurements like neutron diffraction to gain a deep insight on the valence of Sm ions.
Heat Capacity Measurements
Heat capacity Cp(T) of the polycrystalline SmNiC2 (black dots) and LaNiC2 (blue solid line) is plotted as a function of temperature in Fig. 6(a). At the highest temperature, Cp (at 300 K) reaches approximately 80% of the value expected by Dulong-Petit law 3nR value ~100 J mol−1K−1, suggesting that the Debye temperature for SmNiC2 exceeds 300 K. A small anomaly at around 153K (inset b) is likely caused by the CDW ordering, although this temperature is 5 K higher than a CDW temperature estimated from the resistivity and magnetization measurements. A huge anomaly is visible at low temperature and details are presented in Fig. 6(c). In the zero-field data, a λ-shape transition occurs at TC = 17 K, which is in agreement with the Curie temperature estimated by resistivity and magnetization techniques. With increasing magnetic field, the transition is broadened and split into two peaks, indicating an additional field-induced phase transition. A simple subtraction of the LaNiC2 specific heat from the SmNiC2 specific heat yields the temperature dependence of the magnetic specific heat (not shown). The integrated entropy, presented in Fig. 6(d), is close to Rln4 at about 150 K, comparable to the CDW transition temperature for SmNiC2. The magnetic entropy recovered at TC ( = 17.1 K) accounts for 80% of Rln2, the entropy expected for the doublet ground state of the J = 5/2 multiplet for Sm3+ (4f 6). Incomplete recovery of the entropy at TC could be ascribed to either the fluctuating valence between Sm3+ and Sm2+ or the Kondo screening effects of Sm 4f spins by the itinerant electrons.
Heat capacity data (Cp/T) for La-rich samples is selectively presented on a semi-logarithmic scale in Fig. 7. A sharp SC transition for LaNiC2 (open circles) is visible at 2.9 K in Fig. 7(a). When Sm is alloyed in LaNiC2, the SC jump in the specific heat is quickly suppressed and there is no signature for the SC transition down to 1.8 K, the lowest measured temperature, for 3% Sm concentration (x = 0.97). With further increasing Sm concentration, the low-temperature specific heat divided by temperature (C/T) increases with decreasing temperature and shows a peak at 14% Sm concentration due to the FM ordering, where the brown vertical line marks the Curie temperature estimated from the Arrott plot of magnetization. Even though the lowest measured temperature is limited to 1.8 K, the singular enhancement in C/T is clearly visible as Sm concentration approaches 10%, indicating the possible presence of a FM quantum critical point at that concentration.
Figure 7(b,c) magnifies the specific heat of LaNiC2 near the SC transition temperature. The normal-state specific heat measured at μ0H = 3 T, shown by open squares in Fig. 7b, was fitted to Cp = γT + βT 3, where the first and second terms represent electronic and lattice contributions, respectively. The fit to these data allows us to estimate γ = 7.3(1) mJ mol−1K−2, and β = 0.088(5) mJ mol−1K−4. The simple Debye model connects the β coefficient and the Debye temperature ΘD through ΘD = (12π4nR/5β)1/3 = 445 K, where R = 8.314 J mol−1K−1 and n is the number of atoms per formula unit (n = 4 for LaNiC2). This value is slightly lower than reported ΘD = 456 K for YNiC2 (ref. 31) and can be explained by a simple mass relationship: larger La mass than Y should result in lower ΘD.
From an equal entropy construction shown by the solid lines in Fig. 7c, superconducting critical temperature was obtained to be Tsc = 2.9 K, which is lower than that from the resistivity measurement (Tsc = 3.4 K). The ratio between the specific heat jump (ΔC) at Tc and the Sommerfeld coefficient (γ), ΔC/γTsc, is 1.33, which is close to the BCS predicted value of 1.42 for a weakly coupled superconductor.
It is interesting to note that the CDW phase is driven by the one-dimensional (1D) anisotropy along the a-axis in the electronic structure7. The 1D anisotropy increases with chemical or physical pressure mainly because the Ni (or Sm) chain along the a-axis is affected the most (either compressed or expanded). The phase diagram for the series Sm1−xLaxNiC2 is shown in Fig. 8. The results from both transport and magnetic measurements are used to plot the phase diagram. In the top panel of Fig. 8, the unit cell volume is plotted against x and y, which evidently shows that both Sm1−xLaxNiC2 and Sm1−yLuyNiC2 follow Vegard’s law. In the bottom plot of Fig. 8, we can see a slight increase in TCDW with the inclusion of Lu in the lattice due to a positive chemical pressure, while there occurs a decrease in TCDW with increase in La due to a negative chemical pressure in the lattice. The CDW transition is getting suppressed from 148 K (x = 0) to 34 K (x = 0.3) with La doping concentration x and completely destroyed for x > 0.3.
When a CDW is present, there is a slight increase in the FM Curie temperature from 17.2 K to 17.8 K (which is confirmed from both transport and magnetic measurements). Recently B-doped SmNiC2 reported a similar increase in TC from 17.5 K to 23.1 K until the CDW is present32. Once a CDW is suppressed in Sm1−xLaxNiC2, however, the Curie temperature starts to decrease and is suppressed down to 2.5 K at x = 0.86. Inset of the bottom panel magnifies the temperature-La concentration phase diagram near the pure LaNiC2, where solid lines are guides to eyes. Both TC and Tsc could be extrapolated to zero Kelvin at x = 0.92, underscoring the possibility of a FM QCP that was proposed by the singular enhancement in the low-T specific heat. Electrical resistivity measurements show that the first-order FM transition in SmNiC2 changes to the second order or a weakly first order for higher La concentration, suggesting that the disorder introduced by La substitution may be important to the realization of the FM QCP in SmNiC2 (see Fig. S4 in the Supplementary Information). In the case of Lu doped SmNiC2, TC is strongly suppressed from 17.5 K to 8.8 K for y = 0.4. As shown in Fig. S2 in the Supplementary Information, however, the disparate resistivity behaviour near TC for y = 0.4 demands further investigation on the precise nature of magnetic ordering for different Lu doped level.
FM ordering persists up to x = 0.92 in LaNiC2-SmNiC2 system, where the dilution of Sm local moments by La substitution exceeds the percolation limit33. Once a CDW is destroyed, the relationship in LaNiC2-SmNiC2 solid solution is almost similar to La-Gd alloy system, where the SC transition temperature of La elemental metal decreases rapidly with increasing Gd content and is completely suppressed at 0.9 at% Gd. La-Gd alloy containing just 3% Gd becomes ferromagnetic at 1.3 K (ref. 29). However, Gd in Y did not show any FM until 10 at% Gd34. With the introduction of other rare earths in binary alloys the Neel and Curie points are generally lowered. We have also synthesized other rare earth substitution such as Y alloying to SmNiC2. For 20% Y concentration, the CDW is completely destroyed and the Curie temperature is also dropped to 10 K (not shown here).
We have successfully synthesized SmNiC2 solid solution with La (or Lu) and investigated the tuneable behaviour from the CDW ferromagnet to the weakly coupled superconductor. La alloying in SmNiC2 expands the lattice parameters (negative pressure), while Lu alloying shrinks the lattice parameters (positive pressure). The CDW transition temperature (TCDW = 148 K) in Sm1−xLaxNiC2 decreases with increasing La inclusion x because of the poor Fermi surface nesting conditions from the La alloying. La (or Lu) alloying also dilutes the density of Sm local moments because there is no f electron in the substituent, therefore suppressing the FM phase. The Curie temperature, however, does not decrease monotonically with La concentration, but shows a maximum near x = 0.3, underscoring that the CDW and ferromagnetic phases compete against each other. Superconductivity is observed only for La rich compounds (x > 0.92), where the SC transition temperature (Tsc = 3.4 K) for LaNiC2 is quickly suppressed with increasing Sm contents and to zero Kelvin near 8% Sm concentration. When combined with the fact that both Curie temperature and SC transition temperature is suppressed to zero Kelvin near xc = 0.92, the singular enhancement of the low-T specific heat at the critical concentration xc points toward the presence of a ferromagnetic quantum critical point (QCP). We note that disorder introduced by the La substitution may be conducive to the realization of the FM QCP in SmNiC2 (ref. 35). More study is in progress to elucidate the nature of the candidate QCP.
The series of compounds Sm1−xLaxNiC2 (0 ≤ x ≤ 1) and Sm1−yLuyNiC2 (0 ≤ y ≤ 0.4) were synthesized by the arc-melting technique, using constituent elements of purity 99.9% or higher. The weight loss after arc melting was less than 1%, indicating that the nominal concentration is close to the actual alloying level. Since WDS analysis corroborates this conclusion, the nominal concentration was used throughout this manuscript. The arc-melted samples were annealed at 1173K for ten days in a sealed evacuated quartz tube. The annealed samples were quenched in NaCl-ice water mixture. Structural characterization was performed by the powder x-ray diffraction (PXRD) method using a Rigaku diffractometer with Cu Kα radiation. The lattice parameters of the samples were determined by LeBail profile refinements of PXRD carried out using the FULLPROF software27. Resistivity measurements were performed using a standard four probe technique employing a Quantum Design Physical Property Measurement System (PPMS). The contacts were made by spot welding of platinum wires on the sample surface. Heat capacity was measured in temperature range 1.9 K < T < 300 K at fields up to 9 T by using the thermal relaxation technique (PPMS system). Magnetic measurements were carried out using a Quantum Design Magnetic Property Measurement System (MPMS).
How to cite this article: Prathiba, G. et al. Tuning the ferromagnetic phase in the CDW compound SmNiC2 via chemical alloying. Sci. Rep. 6, 26530; doi: 10.1038/srep26530 (2016).
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This work was supported by a NRF grant funded by the Ministry of Science, ICT and Future Planning of Korea (No. 2012R1A3A2048816). The research performed at Gdansk University of Technology was financially supported by the National Science Centre (Poland) Grant No. DEC-2012/07/E/ST3/00584.
The authors declare no competing financial interests.
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Prathiba, G., Kim, I., Shin, S. et al. Tuning the ferromagnetic phase in the CDW compound SmNiC2 via chemical alloying. Sci Rep 6, 26530 (2016). https://doi.org/10.1038/srep26530
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