We present a study on the impact of Mn3+ substitution in the geometrically frustrated Ising garnet Ho3Ga5O12 using bulk magnetic measurements and low temperature powder neutron diffraction. We find that the transition temperature, TN = 5.8 K, for Ho3MnGa4O12 is raised by almost 20 when compared to Ho3Ga5O12. Powder neutron diffraction on Ho3MnxGa5−xO12 (x = 0.5, 1) below TN shows the formation of a long range ordered ordered state with k = (0,0,0). Ho3+ spins are aligned antiferromagnetically along the six crystallographic axes with no resultant moment while the Mn3+ spins are oriented along the body diagonals, such that there is a net moment along [111]. The magnetic structure can be visualised as ten-membered rings of corner-sharing triangles of Ho3+ spins with the Mn3+ spins ferromagnetically coupled to each individual Ho3+ spin in the triangle. Substitution of Mn3+ completely relieves the magnetic frustration with f=θCW/TN≈1.1 for Ho3MnGa4O12.
@article{arxiv.1710.05083,
title = {Relieving the frustration through Mn$^{3+}$ substitution in Holmium Gallium Garnet},
author = {P. Mukherjee and H. F. J. Glass and E. Suard and S. E. Dutton},
journal= {arXiv preprint arXiv:1710.05083},
year = {2017}
}
Comments
19 pages, 3 figures, 4 supplementary figures, accepted for publication in Physical Review B as a Rapid Communication