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arXiv · 1309.1100

Lattice effects in the quasi-two-dimensional valence-bond-solid Mott insulator EtMe$_3$P[Pd(dmit)$_2$]$_2$

Rudra Sekhar Manna·Mariano de Souza·Reizo Kato·Michael Lang
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Abstract

The organic charge-transfer salt EtMe$_3$P[Pd(dmit)$_2$]$_2$ is a quasi-two-dimensional Mott insulator with localized spins $S$ = 1/2 residing on a distorted triangular lattice. Here we report measurements of the uniaxial thermal expansion coefficients $α_i$ along the in-plane $i$ = $a$- and $c$-axis as well as along the out-of-plane $b$-axis for temperatures 1.4\,K $\leq $T$ \leq$ 200\,K. Particular attention is paid to the lattice effects around the phase transition at $T_{VBS}$ = 25\,K into a low-temperature valence-bond-solid phase and the paramagnetic regime above where effects of short-range antiferromagnetic correlations can be expected. The salient results of our study include (i) the observation of strongly anisotropic lattice distortions accompanying the formation of the valence-bond-solid, and (ii) a distinct maximum in the thermal expansion coefficients in the paramagnetic regime around 40\,K. Our results demonstrate that upon cooling through $T_{VBS}$ the in-plane $c$-axis, along which the valence bonds form, contracts while the second in-plane $a$-axis elongates by the same relative amount. Surprisingly, the dominant effect is observed for the out-of-plane $b$-axis which shrinks significantly upon cooling through $T_{VBS}$. The pronounced anomaly in $α_i$ around 40\,K is attributed to short-range magnetic correlations. It is argued that the position of this maximum, relative to that in the magnetic susceptibility around 70\,K, speaks in favor of a more anisotropic triangular-lattice scenario for this compound than previously thought.

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Rudra Sekhar Manna, Mariano de Souza, Reizo Kato, Michael Lang. 2013-12-17. Lattice effects in the quasi-two-dimensional valence-bond-solid Mott insulator EtMe$_3$P[Pd(dmit)$_2$]$_2$. https://doi.org/10.1103/physrevb.89.045113

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