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NMR evidence for very slow carrier density fluctuations in the organic metal (TMTSF)$_2$ClO$_4$

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 Added by Fan Zhang
 Publication date 2005
  fields Physics
and research's language is English




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We have investigated the origin of the large increase in spin-echo decay rates for the $^{77}$Se nuclear spins at temperatures near to $T=30K$ in the organic superconductor (TMTSF)$_2$ClO$_4$. The measured angular dependence of $T_2^{-1}$ demonstrates that the source of the spin-echo decays lies with carrier density fluctuations rather than fluctuations in TMTSF molecular orientation. The very long time scales are directly associated with the dynamics of the anion ordering occurring at $T=25K$, and the inhomogeneously broadened spectra at lower temperatures result from finite domain sizes. Our results are similar to observations of line-broadening effects associated with charge-ordering transitions in quasi-two dimensional organic conductors.



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Complementary $^{77}$Se nuclear magnetic resonance (NMR) and electrical transport have been used to correlate the spin density dynamics with the subphases of the field-induced spin density wave (FISDW) ground state in tmt. We find that the peaks in the spin-lattice relaxation rate 1/T$_1$ appear within the metal-FISDW phase boundary and/or at first-order subphase transitions. In the quantum limit above 25 T, the NMR data gives an insight into the FISDW electronic structure.
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Magnetoresistance measurements have been carried out along the highly conducting a axis in the FISDW phase of hydrogened and deuterated (TMTSF)$_2$ClO$_4$ for various cooling rates through the anion ordering temperature. With increasing the cooling rate, a) the high field phase boundary $beta_{rm {HI}}$, observed at 27 T in hydrogened samples for slowly cooled, is shifted towards a lower field, b) the last semimetallic SDW phase below $beta_{rm {HI}}$ is suppressed, and c) the FISDW insulating phase above $beta_{rm {HI}}$ is enhanced in both salts. The cooling rate dependence of the FISDW transition and of $beta_{rm {HI}}$ in both salts can be explained by taking into account the peculiar SDW nesting vector stabilized by the dimerized gap due to anion ordering.
An instrumentation problem with the signal acquisition at high frequencies was discovered and we no longer believe that the experimental data presented in the manuscript, showing a frequency enhancement of the elastoresistivity, are correct. After correcting the problem, the elastoresistivity data is frequency independent in the range investigated. Therefore, the authors have withdrawn this submission. We would like to thank Alex Hristov, Johanna Palmstrom, Josh Straquadine and Ian Fisher (Stanford) for the kind discussions and assistance we received which helped us identify these problems.
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