Issue 12, 2015

A terbium rich orthoborate LiSrTb2(BO3)3 and its analogues

Abstract

A terbium rich orthoborate, LiSrTb2(BO3)3, has been successfully synthesized by a solid state reaction and crystallized from a high temperature flux. Single crystal X-ray diffraction results show that LiSrTb2(BO3)3 possesses the P[3 with combining macron]m1 space group, with cell parameters of a = 10.3845(4) Å, c = 6.4739(8) Å, and Z = 3. In the structure, the terbium atom coordinates to eight oxygen atoms to yield a TbO8 polyhedron. These polyhedra are connected with each other to form a layer of trigonal [Tb3O21] and hexagonal [Tb6O33] blocks in the ab plane, and then the layers are further linked by the triangular BO3 groups along the c direction. The magnetic susceptibility measurements show that LiSrTb2(BO3)3 exhibits paramagnetic behaviors from 2 K to 300 K. The diffuse optical reflection spectrum indicates that LiSrTb2(BO3)3 is transparent in the range 500–1500 nm, and effective green emission is detected in the photoluminescence of LiSrTb2(BO3)3. In addition, a series of isostructural lanthanide analogues LiSrLn2(BO3)3 (Ln = Pr, Nd, Sm–Lu) and LiBaLn2(BO3)3 (Ln = Pr, Nd, Sm–Tm) have also been prepared by solid state reactions.

Graphical abstract: A terbium rich orthoborate LiSrTb2(BO3)3 and its analogues

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2015
Accepted
22 Sep 2015
First published
23 Sep 2015

New J. Chem., 2015,39, 9389-9395

Author version available

A terbium rich orthoborate LiSrTb2(BO3)3 and its analogues

P. Chen, M. Xia and R. K. Li, New J. Chem., 2015, 39, 9389 DOI: 10.1039/C5NJ01913C

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