Eur. Phys. J. B (2014) 87: 256
https://doi.org/10.1140/epjb/e2014-50499-y

Regular Article

Hard X-ray photoemission study of the Fabre salts (TMTTF)₂X (X = SbF₆ and PF₆)

¹ Institut für Physik, Johannes Gutenberg-Universität, 55099 Mainz, Germany
² Instituto de Geociências e Ciências Exatas – IGCE, Unesp – Univ Estadual Paulista, Departamento de Física, Caixa Postal 178, 13506-900 Rio Claro ( SP), Brazil
³ Deutsches Elektronen-Synchrotron DESY, Notkestr. 85, 22607 Hamburg, Germany
⁴ Physikalisches Institut, Goethe-Universität, 60438 Frankfurt, Germany
⁵ Laboratoire de Physique des Solides, Université Paris-Sud, CNRS UMR-8502, 91405 Orsay, France

^a e-mail: medyanyk@uni-mainz.de

Received: 24 July 2014
Received in final form: 15 September 2014
Published online: 3 November 2014

Abstract

Core-level photoemission spectra of the Fabre salts with X = SbF₆ and PF₆ were taken using hard X-rays from PETRA III, Hamburg. In these salts TMTTF layers show a significant stack dimerization with a charge transfer of 1e per dimer to the anion SbF₆ or PF₆. At room temperature and slightly below the core-level spectra exhibit single lines, characteristic for a well-screened metallic state. At reduced temperatures progressive charge localization sets in, followed by a 2nd order phase transition into a charge-ordered ground state. In both salts groups of new core-level signals occur, shifted towards lower kinetic energies. This is indicative of a reduced transverse-conductivity across the anion layers, visible as layer-dependent charge depletion for both samples. The surface potential was traced via shifts of core-level signals of an adsorbate. A well-defined potential could be established by a conducting cap layer of 5 nm aluminum which appears “transparent” due to the large probing depth of HAXPES (8–10 nm). At the transition into the charge-ordered phase the fluorine 1s line of (TMTTF)₂SbF₆ shifts by 2.8 eV to higher binding energy. This is a spectroscopic fingerprint of the loss of inversion symmetry accompanied by a cooperative shift of the SbF₆ anions towards the more positively charged TMTTF donors. This shift does not occur for the X = PF₆ compound, most likely due to smaller charge disproportion or due to the presence of charge disorder.