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We report measurements of the low temperature magnetization $M$ and specific heat $C$ as a function of temperature and magnetic field of the quasi-one-dimensional spin chain, heavy fermion compound YbFe$_5$P$_3$, which resides close to a quantum critical point. The results are compared to the predictions of scaling laws obtained from a generalized free energy function expected near an antiferromagnetic quantum critical point (AFQCP). The scaling behavior depends on the dimensionality $d$ of the fluctuations, the coherence length exponent $\nu$, and the dynamic exponent $z$. The free energy treats the magnetic field as a relevant renormalization group variable, which leads to a new exponent $\phi=\nu z_h$, where $z_h$ is a dynamic exponent expected in the presence of a magnetic field. When $z_h=z$, $T/H$ scaling is expected, as observed in several compounds close to a QCP; whereas in YbFe$_5$P$_3$, a $T/H^{3/4}$ dependence of the scaling is observed. This dependence reflects the relationship $z_h=(4z/3)$ and a field exponent $\phi =4/3$. A feature of the scaling law is that it restricts the possible values of the exponents to two cases for YbFe$_5$P$_3$: $d$=1, $\nu$=1, $z$=1, and $d$=2, $\nu$=1/2, $z$=2., Comment: 17 pages (including Supplemental Material)

Effective models focused on pertinent low-energy degrees of freedom have substantially contributed to our qualitative understanding of quantum materials. An iconic example, the Kondo model, was key to demonstrating that the rich phase diagrams of correlated metals originate from the interplay of localized and itinerant electrons. Modern electronic structure calculations suggest that to achieve quantitative material-specific models, accurate consideration of the crystal field and spin-orbit interactions is imperative. This poses the question of how local high-energy degrees of freedom become incorporated into a collective electronic state. Here, we use resonant inelastic x-ray scattering (RIXS) on CePd$_3$ to clarify the fate of all relevant energy scales. We find that even spin-orbit excited states acquire pronounced momentum-dependence at low temperature - the telltale sign of hybridization with the underlying metallic state. Our results demonstrate how localized electronic degrees of freedom endow correlated metals with new properties, which is critical for a microscopic understanding of superconducting, electronic nematic, and topological states.

Quantum critical points (QCPs) are widely accepted as a source of a diverse set of collective quantum phases of matter. A central question is how the order parameters of phases near a QCP interact and determine the fundamental character of the critical dynamics which drive the quantum critical behavior. One of the most interesting proposals for the quantum critical behavior that occurs in correlated electron systems is that the behavior may arise from local, as opposed to long wavelength, critical fluctuations of the order parameter. The local criticality is believed to give rise to energy over temperature ($E/T$) scaling of the dynamic susceptibility with a fractional exponent near the quantum critical point (QCP). Here we show that $E/T$ scaling is indeed observed for CeCu$_{6-x}$Ag$_x$ but on closer inspection, the fluctuations can be separated into two components, implying that multiple order parameters play an important role in the unconventional critical behavior. Additionally, when the fluctuations corresponding to the magnetically ordered side of the phase diagram are separated, they are found to be three dimensional and to obey the scaling behavior expected for long wavelength fluctuations near an itinerant antiferromagnetic QCP., Comment: 12 pages, 11 figures

In their recent paper [S\"oderlind, P. et al., Sci. Rep. 5, 15958 (2015)], S\"oderlind et al. discuss two subjects from a theoretical point of view: the phonon spectra and the possible magnetic structure of {\delta}-plutonium (Pu). Here, we comment on the second subject. S\"oderlind et al. compare the Pu magnetic form factor F(Q) calculated via density functional theory (DFT) with measurements of F(Q) by neutron spectroscopy [Janoschek, M. et al., Sci. Adv. 1, e1500188 (2015)]. In particular, this comparison does not consider a number of experimental facts established in the neutron spectroscopy study., Comment: 5 pages, 1 figure

A central issue in material science is to obtain understanding of the electronic correlations that control complex materials. Such electronic correlations frequently arise due to the competition of localized and itinerant electronic degrees of freedom. While the respective limits of well-localized or entirely itinerant ground states are well-understood, the intermediate regime that controls the functional properties of complex materials continues to challenge theoretical understanding. We have used neutron spectroscopy to investigate plutonium, which is a prototypical material at the brink between bonding and non-bonding configurations. Our study reveals that the ground state of plutonium is governed by valence fluctuations, that is, a quantum-mechanical superposition of localized and itinerant electronic configurations as recently predicted by dynamical mean field theory. Our results not only resolve the long-standing controversy between experiment and theory on plutonium's magnetism, but also suggest an improved understanding of the effects of such electronic dichotomy in complex materials., Comment: 29 pages, 2 figures, 2 tables, supplementary materials