Abstract
The point at absolute zero where matter becomes unstable to new forms of order is called a quantum critical point (QCP). The quantum fluctuations between order and disorder1,2,3,4,5 that develop at this point induce profound transformations in the finite temperature electronic properties of the material. Magnetic fields are ideal for tuning a material as close as possible to a QCP, where the most intense effects of criticality can be studied. A previous study6 on the heavy-electron material YbRh2Si2 found that near a field-induced QCP electrons move ever more slowly and scatter off one another with ever increasing probability, as indicated by a divergence to infinity of the electron effective mass and scattering cross-section. But these studies could not shed light on whether these properties were an artefact of the applied field7,8, or a more general feature of field-free QCPs. Here we report that, when germanium-doped YbRh2Si2 is tuned away from a chemically induced QCP by magnetic fields, there is a universal behaviour in the temperature dependence of the specific heat and resistivity: the characteristic kinetic energy of electrons is directly proportional to the strength of the applied field. We infer that all ballistic motion of electrons vanishes at a QCP, forming a new class of conductor in which individual electrons decay into collective current-carrying motions of the electron fluid.
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Acknowledgements
We acknowledge discussions with J. Ferstl, C. Langhammer, S. Mederle, N. Oeschler, I. Zerec, G. Sparn, O. Stockert, M. Abd-Elmeguid, J. Hopkinson, A. I. Larkin and I. Paul. Work at Dresden is partially supported by the Fonds der Chemischen Industrie and by the FERLIN project of the European Science Foundation. P. C. is supported by the National Science Foundation. Y. T. is a Young Scientist Research Fellow supported by the Japan Society for the Promotion of Science.
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Custers, J., Gegenwart, P., Wilhelm, H. et al. The break-up of heavy electrons at a quantum critical point. Nature 424, 524–527 (2003). https://doi.org/10.1038/nature01774
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DOI: https://doi.org/10.1038/nature01774
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