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# Magnetic resonance as a local probe for kagomé magnetism in Barlowite Cu4(OH)6FBr

## Abstract

Temperature- and field-dependent 1H-, 19F-, and 79,81Br-NMR measurements together with zero - field 79,81Br-NQR measurements on polycrystalline samples of barlowite, Cu4(OH)6FBr are conducted to study the magnetism and possible structural distortions on a microscopic level. The temperature dependence of the 79,81Br-NMR spin-lattice relaxation rates 1/T1 indicate a phase transition at TN$$\simeq$$ 15 K which is of magnetic origin, but with an unusually weak slowing down of fluctuations below TN. Moreover, 1/T1T scales linear with the bulk susceptibility which indicates persisting spin fluctuations down to 2 K. Quadupolare resonance (NQR) studies reveal a pair of zero-field NQR- lines associated with the two isotopes of Br with the nuclear spins of I = 3/2. Quadrupole coupling constants of vQ 28.5 MHz and 24.7 MHz for 79Br- and 81Br-nuclei are determined from Br-NMR and the asymmetry parameter of the electric field gradient was estimated to η 0.2. The Br-NQR lines are consistent with our findings from Br-NMR and they are relatively broad, even above TN. This broadening and the relative large η value suggests a symmetry reduction at the Br- site reflecting the presence of a local distortion in the lattice. Our density-functional calculations show that the displacements of Cu2 atoms located between the kagome planes do not account for this relatively large η. On the other hand, full structural relaxation, including the deformation of kagome planes, leads to a better agreement with the experiment.

## Introduction

Magnetic frustration, the competing interactions between the spins enhances the quantum fluctuations and leads to exotic ground states and novel phases. One of the important manifestation is the formation of the quantum spin liquid (QSL) ground state1,2,3,4, a highly entangled spin state without any symmetry breaking even at zero temperature. The important reported examples include the two-dimensional kagome lattice quantum magnet Herbertsmithite ZnCu3(OH)6Cl25,6,7, the triangular lattice organic magnets κ–(BEDT-TTF2Cu2(CN)3 and EtMe3Sb[Pd(dmit)2]28,9, and three-dimensional hyperkagome iridate Na4Ir3O810. The quest for more experimental QSL candidates has triggered the intense research in two dimensional kagome lattice systems with spin-$$\tfrac{1}{2}$$ connectivity.

Barlowite, Cu4(OH)6FBr is a structural analog of Herbertsmithite which recently has attracted much attention as a geometrically perfect spin-$$\tfrac{1}{2}$$ kagome antiferromagnet due to an absent antisite disorder (Zn – Cu)11,12,13,14,15,16. Barlowite crystalizes in a hexagonal structure (space group P63/mmc) with lattice parameters $$a\simeq 6.6786\,\AA$$ and $$c\simeq 9.2744\,\AA$$. As shown in Fig. 1, crystallographically equivalent three Cu(1)2+-ions in the chemical formula form the kagome layer in the ab-plane, whereas the fourth Cu(2)2+-ion in the chemical formula occupies the inter-layer sites. The interlayer site is quite large and the fourth Cu(2)2+-ion occupies one out of the three possible equivalent positions which might originate some local distortion of the lattice and a symmetry breaking.

The lattice structure of barlowite is close to that of Herbertsmithite, but has a different stacking pattern of kagome layers because of the different bonding environment of halogen ions. In Herbertsmithite, Cl- ions form both covalent and hydrogen bonds and this lead to a horizontal staggering of kagome layers. In the case of barlowite, Br forms six covalent bonds with Cu2+-ions whereas F-ions form six hydrogen bonds and features a perfect alignment of kagome layers on top of each other. The magnetic exchange between the intralayer (Cu1) and the interlayer (Cu2) Cu2+-ions in barlowite is rather complex12. The low temperature magnetism and in particular the magnetic order is determined by the presence of the interlayer Cu2 ions and their ferromagnetic coupling to the intralayer Cu1 ions. In the antiferromagnetic kagome layer the Cu1 moments are highly frustrated with a rather high coupling constant of about 170 K. Canted antiferromagnetic order at TN ≈ 15 K is revealed from bulk probes at small magnetic fields11 wheras at higher fields a significant ferromagnetic contribution is observed in the bulk magnetization. Susceptibility measurements on polycrystalline material provides a large antiferromagnetic Curie-Weiss temperature of θCW = −136 ± 10 K with a small hysteresis in the magnetization curve (see supplemental material). The possibility of a QSL ground state (of Cu1 Kagome moments) coexisting with ordered Cu2 interlayer moments is discussed in the literatures11,15. Recent studies for barlowite on the Zn substitution on the Cu2 site support this idea. Here magnetic order is suppressed and the fully substituted Zn barlowite Cu3Zn(OH)6FBr is considered as a QSL system16,17,18 very similar to the fully Zn substituted Herbertsmithite Cu3Zn(OH)6Cl2.

The nuclear magnetic resonance (NMR) is a microscopic probe for static and dynamic magnetism and was successfully applied on Herbertsmithite and its polymorphs19,20,21 but so far due to the lack of sizable amounts of pure polycristalline material no NMR study was conducted on barlowite. Whereas the moment transfer from the magnetic ion originates the NMR shift K which provides information about the intrinsic static spin susceptibility χ(q = 0, ω = 0) and the spin-lattice relaxation rate 1/T1 supplies the information about excitations in particular about the dynamic complex susceptibility χ′(q, ω). In this paper, we use magnetic resonance as a local probe for magnetism and simultaneously for the local structure around the NMR active nuclei. In contrast to NMR studies on herbertsmithite, barlowite contains a novel NQR nuclei (Br) which hosts a large quadrupole moment and therefore allows for rather sensitive NQR studies as a measure of lattice distortions and to evidence the claim of the perfect kagome motif. In general, the nuclear spin resonance spectra of nuclei with $$I > \tfrac{1}{2}$$ contains additional information (beside the magnetic interaction mentioned before) due to the presence of the quadrupole interaction. Here the $$I > \tfrac{1}{2}$$ NMR active nuclei has a quadrupole moment which is exposed to the electric field of the surrounding ions (frequently modelled by the point charge model). Therefore the quadrupole interaction depend in first place on the electric field gradient at the nucleus site (charge distribution around the nucleus) and the quadrupole moment of the nucleus itself. As for NMR the main interaction is the magnetic one (Zeeman interaction) and the quadrupole interaction is just a perturbation the NQR technique (at zero field) is more favorable to probe the quadrupole interaction solely. Two $$I=\tfrac{3}{2}$$-isotopes with 100% natural abundance in total and relatively large quadrupole moments on both nuclei identifies Br- NMR and NQR as a powerful technique which is frequently applied on quantum spin systems and other forms of matter22,23,24,25. Our Br magnetic resonance study presented here aims for the consistent determination of the quadrupole coupling constant νQ and the asymmetry parameter η from NMR and NQR.

## Results and Discussion

Figure 2 shows the field sweep 1H- and 19F-NMR spectra measured at a fixed frequency of 84.44 MHz for different temperatures. No shift in the central peak position was observed for the 1H-line, whereas a small shift was found for the 19F-line. Both NMR lines show a significant broadening below 15 K which is consistent with the magnetic order at 15 K (see supplementary materials Fig. S1)11. The NMR Knight shift K(T) = [Href − H*(T)]/H*(T) was determined by measuring the resonance field of the sample, H*(T) as a function of the temperature with respect to the nonmagnetic reference sample (resonance field Href). The temperature-dependent K(T) of 19F line is presented in the Fig. 2(b). It shows a Curie-Weiss behaviour similar to the χ(T) data (see supplemental material). Generally, K(T) is directly proportional to the spin susceptibility (χspin) and can be written as $$K(T)={K}_{0}+\frac{{A}_{{\rm{hf}}}}{{N}_{A}}{\chi }_{{\rm{spin}}}$$, where K0 is the temperature independent orbital (chemical) shift, NA is the Avogadro number, and Ahf is the hyperfine coupling constant between the 19F nucleus and the Cu2+ magnetic moments. The conventional scheme for calculating Ahf is to take the slope of the K vs. χ plot with T as an implicit parameter. As shown in Fig. 2(c), the K vs. χ plot is fitted very well by a linear behaviour over a wide temperature range yielding Ahf ≈ 950 Oe/μB and K0 ≈ −0.05%.

The 1H- and 19F-NMR lines were found to broaden monotonously upon lowering the temperature. The 1H-NMR line width $${\rm{\Delta }}\nu =\frac{\gamma }{2\pi }{\rm{\Delta }}H$$ (defined as the full width half maximum, FWHM) as a function of temperature is shown in Fig. 3. Δν is increasing systematically with decreasing temperature and tracks the magnetic susceptibility. For a comparison, in the same Fig. 3, χ(T) measured at 2 T is also plotted in the right y-axis. The NMR spectral width has two major contributions, (i) the dipolar interaction between the nuclei and (ii) the dipolar interaction of the 1H-nuclei with the neighboring Cu2+ magnetic ions and can be expressed as, Δν = Δν0 + Δνaniso. The first term is a temperature and field independent contribution from the nuclear-nuclear dipolar interaction, whereas the second term is the powder average over the anisotropic dipolar interaction between the 1H-nuclei and magnetic Cu2+-ions which is T- dependent. In an external magnetic field, this anisotropic coupling gives rise to inhomogeneous line broadening which is proportional to the bulk magnetic susceptibility χ(T). So one can write as26,27,28,29,

$$\frac{{({\rm{\Delta }}\nu )}_{{\rm{aniso}}}}{{\nu }_{{\rm{L}}}}={A}_{{\rm{z}}}\chi \approx \frac{\langle \mu \rangle }{{r}^{3}H}$$

where $${\nu }_{L}=\frac{{\gamma }_{{\rm{N}}}}{2\pi }H$$ denotes the 1H Larmor frequency for an applied external magnetic field H, Az is the average dipolar coupling constant between the 1H nucleus and magnetic Cu2+ ions, and r is the average distance between them. Finally, we can rewrite

$${\rm{\Delta }}\nu ={\rm{\Delta }}{\nu }_{0}+\frac{{\gamma }_{{\rm{N}}}}{2\pi }{A}_{{\rm{z}}}H\chi .$$
(1)

In the inset of Fig. 3 we plotted Δν versus χ with temperature as an implicit parameter and it follows a linear behaviour. This linear Δν vs. χ is fitted by Eq. 1 and the obtained value of dipolar coupling constant Az ~ 1022 cm−3 corresponds to the field generated by the Cu2+-moments at an average distance of 3 Å. This suggests that the interaction of the 1H-nucleus with Cu2+ moments is largely of dipolar origin.

Figure 4(a) shows the field sweep Br- NMR spectra measured at 84.44 MHz at different temperatures. Multiple lines are found corresponding to both 79Br- and 81Br- isotopes exposed to first- and second- order quadrupole interaction and with powder averaged intensity. At high temperatures, Br- sites yield a complex NMR spectra consist of splitted central lines with broad satellites. The central line arises from the (+$$\tfrac{1}{2}$$$$\to$$ −$$\tfrac{1}{2}$$) transition split into two peaks due to the combined effect of magnetic anisotropy and second order quadrupolar interaction. No significant shift was observed with temperature, which reflects a weak transferred hyperfine coupling of the 79,81Br nuclei with the Cu2+ spins. The spectra starts to broaden with decrease in temperature. Both 79Br- and 81Br- are quadrupole nuclei with nuclear spin $$I=\tfrac{3}{2}$$ and gyromagnetic ratio γ/2π = 10.666 MHz/T and 11.498 MHz/T, respectively. For a quadrupole nuclei, the nuclear spin Hamiltonian can be expressed as a summation of the Zeeman interaction and the quadrupole interaction as H = HZ + HQ, where HZ = −γIHeff represents the zeeman term and $${H}_{{\rm{Q}}}=\frac{h{\nu }_{{\rm{Q}}}}{6}[3{I}_{Z}^{2}-I(I+1)+\frac{1}{2}\eta ({I}_{x}^{2}-{I}_{y}^{2})]$$. Heff is the effective field which is the sum of external field H and the hyperfine field Hhy at the Br site, νQ = 3eQVzz/2hI(2I − 1) is the quadrupole coupling constant, Vzz is the largest component of electric field gradient (EFG) tensor, and eQ is the nuclear quadrupole moment. The EFG tensor is generally defined as Vzz| ≥ |Vyy| ≥ |Vxx| with η = (Vxx − Vyy)/Vzz as the asymmetry parameter30,31. When the quadrupole term in the Hamiltonian is weak compared to the Zeeman term, the quadrupolar term modifies the NMR spectrum and can be treated as a first order perturbation. In this case, the position of the central line ($$\tfrac{1}{2}$$$$\leftrightarrow$$ −$$\tfrac{1}{2}$$ transition) is determined by the applied magnetic field whereas the distance between the satellite lines (corresponding to the −$$\tfrac{3}{2}$$$$\leftrightarrow$$ −$$\tfrac{1}{2}$$ and $$\tfrac{3}{2}$$$$\leftrightarrow$$$$\tfrac{1}{2}$$ transitions) depend on the angle θ between the magnetic field direction and the direction of the maximum of the EFG component Vzz. When quadrupole effects are considered to second order (and for axial symmetry), the central line position (in the absence of anisotropy) also depends on θ and is given by

$${\nu }_{(\pm \frac{1}{2})}={\nu }_{0}+\frac{{\nu }_{Q}^{2}}{32{\nu }_{0}}[I(I+1)-\frac{3}{4}]\,(1-{co}{{s}}^{2}\,\theta )\,(9\,{co}{{s}}^{2}\,\theta -1),$$
(2)

where ν0 the Larmor frequency. For a randomly aligned polycrystalline sample the central line shape is the powder average, resulting in two peaks corresponding to $$\theta \simeq 41.8^\circ$$ and $$\theta \simeq 90^\circ$$32.

At 30 K, the spectra was fitted reasonably well, taking into account the second-order quadrupolar perturbation contribution. Figure 4(b) shows the measured spectra at 30 K together with the theoretical simulation. The parameters obtained are $${K}_{{\rm{iso}}}\simeq -\,\mathrm{0.73 \% }$$, $${K}_{{\rm{ax}}}\simeq \mathrm{0.185 \% }$$, $$\eta \simeq 0.2$$, and $${\nu }_{Q}\simeq 28.5\,{\rm{MHz}}$$ for 79Br line and $${K}_{{\rm{iso}}}\simeq -\,\mathrm{0.74 \% }$$, $${K}_{{\rm{ax}}}\simeq \mathrm{0.2 \% }$$, $$\eta \simeq 0.2$$, and $${\nu }_{Q}\simeq 24.7\,{\rm{MHz}}$$ for 81Br line. As both isotopes are exposed to the same electric field gradient, the ratio 79νQ/81νQ gives the ratio of their qudrupole moments.

Both the isotopes of bromine are quadrupole nuclei and have large quadrupole moment (79Q = 0.33 × 10−28 m2 and 81Q = 0.28 × 10−28 m2) and almost same natural abundance. For spin-$$\tfrac{3}{2}$$ nuclei, which have two doubly degenerate energy levels,

$${E}_{\pm \frac{3}{2}}=\frac{h{\nu }_{Q}}{2}{(1+\frac{{\eta }^{2}}{3})}^{\frac{1}{2}},{E}_{\pm \frac{1}{2}}=-\,\frac{h{\nu }_{Q}}{2}{(1+\frac{{\eta }^{2}}{3})}^{\frac{1}{2}}$$

and the only one pure quadrupole resonance frequency can be obtained as $${\nu }_{{\rm{NQR}}}={\nu }_{Q}{(1+{\eta }^{2}/3)}^{\frac{1}{2}}$$33. The NQR spectrum measured at 30 K is shown in Fig. 4(c). We observed a broad spectrum which is the combination of two lines at νNQR = 28.3 MHz and 24.5 MHz corresponding to the 79Br and 81Br quadrupole resonance, respectively. The ratio of the resonance frequencies and the intensities of the lines correlate well with the ratio of the quadrupole moments and the natural abundance for 79Br and 81Br isotopes, respectively. The resonance frequencies are also consistent with the parameter obtained from the NMR spectral simulation at 30 K.

Br atoms occupy the 2c position with the $$\bar{6}$$m2 symmetry in the hexagonal structure of barlowite, so their EFG asymmetry should be zero. The non-zero η value is indicative of deviations from the hexagonal symmetry caused by the displacement of Cu2 atoms away from the three-fold axis. The influence of this displacement on the electric field gradient was explored by density-functional (DFT) calculations that arrived at η = 0.08 for Br. Local displacements of Cu2 may also affect the positions of other atoms, resulting in deviations from the average hexagonal crystal structure. To gain further insight into these structural changes, we performed full relaxation and optimized all atomic coordinates until energy minimum was reached. This led to two possible configurations (see Methods) with slightly different η’s of 0.12 and 0.18, both approaching the experimental $$\eta \simeq 0.2$$. We thus show that the displacements of Cu2 do not account for the full experimental EFG asymmetry. The displacements of others atoms contribute as well. The local structure of barlowite may not be well described by the average hexagonal model, a conclusion that goes in line with the very recent diffraction studies reporting orthorhombic symmetry of the crystal structure34,35.

Insights into the spin dynamics can be obtained by measuring the spin lattice relaxation rates (1/T1) as a function of temperature. 79Br and 81Br nuclear spin-lattice relaxation time T1 were measured using a conventional inversion recovery pulse sequence at 84.44 MHz (at 7.4 T for 81Br and 8.2 T for 79Br). Values of T1 were obtained from fits to an appropriate relaxation function. The recovery of the longitudinal magnetization M(t) at a time delay t after the inversion pulse could be fitted consistently with a single T1 function; $$(1-\frac{M(t)}{M(\infty )})=0.1\,\exp [\,-\,{(t/{T}_{1})}^{\beta }]+0.9\,\exp [\,-\,{(6t/{T}_{1})}^{\beta }]$$, where β is the stretch exponent. The temperature dependence of 1/T1 is shown in Fig. 5(a). At high temperatures (T ≥ 20 K), 1/T1 is almost temperature-independent (in the paramagnetic regime) for both isotopes, which is often observed in a system with localized moments when the temperature is higher than the exchange energy between the spins36. With decreasing temperatures, 1/T1 shows an anomaly at $${T}_{{\rm{N}}}\simeq 15\,{\rm{K}}$$ associated with some sort of phase transition consistent with the thermodynamic measurements11. Below TN, 1/T1 decreases smoothly towards zero as a result of the disappearance of the critical fluctuations in the ordered state. The overall behaviour of temperature dependence of 1/T1 is similar for both the isotopes. In order to understand the relaxation mechanism, we have measured 1/T1 for both isotopes at the same applied magnetic field. In the case of a pure magnetic relaxation mechanism, the ratio of the relaxation rates should be equal to the ratio of the squares of corresponding gyromagnetic ratio, (79γ/81γ)2 ≈ 0.85. Whereas, for a pure quadrupole relaxation mechanism, the ratio of relaxation rates will be equal to the ratio of the squares of their quadrupole moments (79Q/81Q)2 ≈ 1.425. In the inset of Fig. 5(a), we have plotted the ratio of relaxation rate of both isotopes, 79R/81R as a function of temperature, where R denotes the spin lattice relaxation rate 1/T1. It is observed that the ratio of the relaxation rates are very close to the value (79γ/81γ)2 ≈ 0.85 indicating the magnetic nature of the relaxation mechanism. Nonetheless it has to be mentioned that the behaviour of 1/T1 in the ordered state is rather unconventional for a bulk ordered antiferromagnet37 and the power law obtained (T0.9) has a rather small exponent. A reduced power law in 1/T1 was even found in Cl NMR on Herbertsmithite which does not show any long range order at all38. Br NMR in barlowite evidences a rather weak slowing down of critical fluctuations towards low temperatures. For Barlowite this might indicates that only a fraction of Cu magnetic moments undergoes long-range magnetic order (f.i. interlayer Cu2 moments), or the ordered moment is rather small, and significant spin fluctuations persist in the ordered state. This is also supported by the magnetization recovery (Fig. 5b). Very recent neutron diffraction studies on the barlowite also support this scenario. Here, strong residue spin fluctuations, in the form of intralayer spin singlet formation due to the structure distortion (both displacements of Cu2 and deformation of kagome planes), are reported below magnetic transition at 15 K35. For systems with unique and homogeneous relaxation rate, the value of the stretch exponent will be β = 1. In contrast, a reduced value of β(<1) indicates a wide distribution of relaxation rates. As shown in Fig. 5(c), the value of β is close to 1 at higher temperatures, but it decreases with decreasing temperature below 20 K. This behaviour is frequently found for frustrated low dimensional quantum magnets where magnetic order competes with persistent liquid like magnetic excitations39,40,41,42.

As shown in Fig. 6, the temperature dependence of 1/T1T gradually increases with decreasing temperature and shows a steep up-turn below around 20 K. This up-turn in 1/T1T below 20 K indicates the typical behaviour near TN due to the critical Cu2+ moment fluctuations. Frequently a scaling with the bulk susceptibility is observed43. The spin-lattice relaxation rate probes the q- averaged low energy spin excitations and can be expressed in terms of imaginary part of the dynamic spin susceptibility $${\chi }_{M}^{^{\prime\prime} }(\overrightarrow{q},{\omega }_{0})$$ as

$$\frac{1}{{T}_{1}T}=\frac{2{\gamma }_{N}^{2}{k}_{B}}{{N}_{{\rm{A}}}^{2}}\,\sum _{\overrightarrow{q}}\,|A(\overrightarrow{q}){|}^{2}\frac{\chi ^{\prime\prime} (\overrightarrow{q},{\omega }_{0})}{{\omega }_{0}},$$
(3)

where the sum is over the wave vectors $$\overrightarrow{q}$$ within the first Brillouin zone, $$A(\overrightarrow{q})$$ is the form factor of the hyperfine interactions as a function of $$\overrightarrow{q}$$, and ω0 is the nuclear Larmor frequency44. In the strict (ferromagnetic) limit of q = 0 and ω0 = 0, the real component of $${\chi }_{M}^{^{\prime} }(\overrightarrow{q},{\omega }_{0})$$ corresponds to the uniform static bulk susceptibility χ and $$1/{T}_{1}T\propto \chi \tau$$ with τ being the on site fluctuation rate is valid43. In the inset of Fig. 6, we show 1/T1T against χ with temperature as an implicit parameter. The linear relation between 1/T1T and χ indicates a constant on site fluctuation rate τ over a wide range in temperature and even trough the transition. This reflects the fact that barlowite is far from being a regular antiferromagnet in particular due to persisting magnetic fluctuations down to low temperatures. It still remains an open question what kind of magnetic order occurs in barlowite below 15 K, and if all Cu moments are part of that order or if for instance only the inter layer Cu2 moments participate and the Cu1 moments in the kagome plane remain fluctuating and spin liquid like towards low temperatures. This scenario is supported by the small entropy found across the transition and the small saturation moment15. Furthermore there are ferro and antiferromagnetic exchange couplings among the two different Cu moments accompanied by a lattice anisotropy12. The static and dynamic (this means excitations) magnetism in barlowite is far from being understood and there is a strong demand for other local probes like neutron scattering or spin Muon resonance (μSR) and for studies on single crystals. As for all herbertsmithite relatives (like barlowite or kapellasite) and planar kagome-like minerals (like volborthite or vesignieite) a combination of local probes is required to disentangle between spin freezing, long-range order and the QSL ground state (see review of P. Mendels and S. Willis21).

## Summary

In conclusion, we investigated the magnetism in the spin-$$\tfrac{1}{2}$$ quantum magnet barlowite Cu4(OH)6FBr via the microscopic NMR and NQR techniques. 1H, 19F, and 79,81Br NMR measurements are performed in a wide temperature and field range together with Br NQR measurements. 1H and 19F NMR results reveal well defined NMR lines and hyperfine coupling parameters. A broadening of the line width of the 1H, 19F, and 79,81Br NMR lines indicate some form of order below 15 K. Spin lattice relaxation rate measurements performed on both Br isotopes reveal a kink which probably indicate magnetic ordering at $${T}_{{\rm{N}}}\simeq 15\,K$$ and which is solely magnetic in origin. The temperature dependence of the spin lattice relaxation rate below 15 K is rather weak (T0.9 power law) and evidences persisting magnetic fluctuations even in the ordered state. NMR studies on single crystals together with inelastic neutron studies would be required to probe the complex magnetic structure below 15 K. Furthermore we performed a comparative NMR and NQR study on both Br isotopes. We have observed a pair of NQR lines corresponding to the 79,81Br nuclei and in good agreement with the complex Br NMR spectra obtained. From our 79,81Br NMR and NQR measurements, we obtain an asymmetry parameter of the electric field gradient $$\eta \simeq 0.2$$ and the quadrupole coupling constants $${\nu }_{Q}\simeq 28.5\,{\rm{MHz}}$$ and 24.7 MHz for 79Br and 81Br nuclei, respectively. The broad NQR spectrum observed at 30 K and the relatively large electric field gradient indicate a symmetry reduction at the Br site which can not be explained by the displacements of Cu2 alone and indicates salient deviations of the barlowite structure from the hexagonal symmetry. Magnetic resonance studies on various nuclei in barlowite evidence that the Cu moment arrangement is far from perfect and that the magnetic excitations are unconventional in nature.

## Methods

Polycrystalline samples of Cu4(OH)6FBr were synthesised by hydrothermal reaction. Copper carbonate hydroxide CuCO3.Cu(OH)2, ammonium fluoride NH4F, and Hydrobromic acid HBr were used as starting materials and sealed in a Teflon-lined stainless steel vessel. The reaction mixture was heated at 393 K for 4 days and then cooled down to room temperature. Blue-green powder of Cu4(OH)6FBr were obtained after filtration and no foreign phases were observed in x-ray diffraction.

Polycrystalline barlowite samples of a few 100 mg are studied through 1H-, 19F-, and 79,81Br-NMR measurements. NMR measurements were performed using a home-built Techmag Apollo spectrometer with a standard local probe and a sweepable superconducting magnet. Field sweep NMR spectra were obtained by the integration of spin echo signals at a fixed frequency. Br-NQR spectra were measured using a frequency step point-by-point spin-echo technique. At each frequency point, the area under the spin-echo real part was integrated after proper phase adjustment in the time domain. Nuclear spin-lattice relaxation rates were measured using a standard inversion recovery method, where the nuclear magnetization M(t) were obtained from the recovery of the spin-echo magnitude as a function of the time interval τ between the inversion pulse (π pulse) and the π/2 − π spin-echo sequence.

Density-functional calculations were performed in the full-potential local-orbital FPLO code45 using the Perdew-Wang flavor of the exchange-correlation potential46. Electric field gradient on the Br site was computed using the internal procedure of FPLO. First, calculations were performed for the experimental atomic positions47 with Cu2 atoms placed into one of the three symmetry-related sites around the three-fold axis. This reduced the symmetry to monoclinic C2/m. Additionally, full structural relaxation was performed, resulting in two minima with nearly equal energies (energy difference of less than 1 meV/f.u.) and different mutual arrangement of the Cu2 atoms. The relaxation introduced deviations from the three-fold symmetry not only at the Cu2 sites, but for all atoms throughout the structure leading to the overall monoclinic symmetry.

### Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

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## Acknowledgements

The authors are grateful to H. Yasuoka, P. Mendels, and R. Stern for fruitful discussions.

## Author information

Authors

### Contributions

M. Baenitz and C. Krellner designed the project. C. Klein synthesized the sample. K.M. Ranjith performed the magnetization, NMR, and NQR measurements. A.A. Tsirlin and H. Rosner performed the DFT calculations. All authors contributed to the analysis and discussions of experimental data. K.M. Ranjith and M. Baenitz wrote the manuscript with the inputs from all other authors.

### Corresponding author

Correspondence to K. M. Ranjith.

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Ranjith, K.M., Klein, C., Tsirlin, A.A. et al. Magnetic resonance as a local probe for kagomé magnetism in Barlowite Cu4(OH)6FBr. Sci Rep 8, 10851 (2018). https://doi.org/10.1038/s41598-018-29080-8

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• DOI: https://doi.org/10.1038/s41598-018-29080-8

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