A series of quaternary selenides, NaGaSe ( = Mn, Fe, and mixed Zn/Fe), have been synthesized for the first time employing a high-temperature solid-state synthesis route through stochiometric or polychalcogenide flux reactions. Along with the selenides, a previously reported sulfide analogue, NaFeGaS, is also revisited with new findings. These compounds form an interpenetrated structure made up of a supertetrahedral unit. The electrochemical evaluations exhibit a reversible (de)intercalation of ∼0.6 and ∼0.45 Na-ions, respectively, from NaFeGaS () and NaFeGaSe () involving Fe/Fe redox when cycled between 1.5 and 2.5 V. Mössbauer spectroscopy of shows the existence of a mixed oxidation state of Fe in the pristine compound and reversible oxidation of Fe to Fe during the electrochemical cycles. NaZnFeGaSe possesses a reasonably high room temperature ionic conductivity of 0.077 ms/cm with an activation energy of 0.30 eV. The preliminary magnetic measurements show a bifurcation of FC-ZFC at 4.5 and 2.5 K, respectively, for and NaMnGaSe () arising most likely from a spin-glass like transition. The high negative values of the Weiss constants -368.15 and -308.43 K for and , respectively, indicate strong antiferromagnetic interactions between the magnetic ions and also emphasize the presence of a high degree of magnetic frustration in these compounds.
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http://dx.doi.org/10.1021/acs.inorgchem.4c00927 | DOI Listing |
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