Search for: All records

Electronic spins can form long-range entangled phases of condensed matter named quantum spin liquids. Their existence is conceptualized in models of two- or three-dimensional frustrated magnets that evade symmetry-breaking order down to zero temperature. Quantum spin ice (QSI) is a theoretically well-established example described by an emergent quantum electrodynamics, with excitations behaving like photon and matter quasiparticles. The latter are fractionally charged and equivalent to the `spinons' emerging from coherent phases of singlets in one dimension, where clear experimental proofs of fractionalization exist. However, in frustrated magnets it remains difficult to establish consensual evidence for quantum spin liquid ground states and their fractional excitations. Here, we use backscattering neutron spectroscopy to achieve extremely high resolution of the time-dependent magnetic response of the candidate QSI material Ce2Sn2O7. We find a gapped spectrum featuring a threshold and peaks that match theories for pair production and propagation of fractional matter excitations (spinons) strongly coupled to a background gauge field. The observed peaks provide evidence for a QSI through spectroscopic signatures of space-time symmetry fractionalization, while the threshold behavior corroborates the regime of strong light-matter interaction predicted for the emergent universe in a QSI. 

We investigate the correlated state of Ce2Hf2O7 using neutron scattering, finding signatures of correlations of both dipolar and octupolar character. A dipolar inelastic signal is also observed, as expected for spinons in a quantum spin ice (QSI). Fits of thermodynamic data using exact diagonalization methods indicate that the largest interaction is an octupolar exchange, with a strength roughly twice as large as other terms. This hierarchy of exchange interactions - far from a perturbative regime but still in the octupolar QSI phase - rationalises observations in neutron scattering, which illustrate the multipolar nature of degrees of freedom in Ce3+ pyrochlores.