At 300 K the Eu2+ ion luminesces efficiently in SrB4O7, and to a lesse
r extent in SrB6O10 and Sr3B2O6. In the last compound the lowest 4f-5d
absorption band is at extremely low energy for Eu2+. Due to this and
a large Stokes shift, the EU2+ emission band has its maximum at 590 nm
. From a comparison with the luminescence of Ce3+ and Pb2+ in this lat
tice it is concluded that a strong non-cubic crystal field splits the
5d excited state, causing the lowest f-d absorption transition to be a
t a low energy position. In SrB2O4 and Sr2B2O5 only Eu3+ was found. An
explanation for this is proposed on the basis of a charge-compensatio
n mechanism for Eu3+; the luminescence of this ion is discussed as wel
l.