The 0.5-eV (4000-cm-1) emission band in InP:Fe is studied in detail by
Fourier-transform infrared photoluminescence (PL), time-resolved PL,
and photoluminescence excitation (PLE) spectroscopy. We resolve new fi
ne structures in both the zero-phonon (ZP) lines and in the correspond
ing phonon sideband. The transient PL signal follows an exponential de
cay with a time constant of 1.1 +/- 0.3 ms. The PLE shows that the 0.5
-eV band can be pumped via hole capture of Fe2+ and even more efficien
tly by exciting resonantly the charge-transfer states [Fe2+ (5T2), h(b
)], where the hole is bound to Fe2+. The results from PLE and the long
decay time strongly support the interpretation of the 0.5-eV band as
spin-flip transitions 4T1 --> 6A1 of Fe3+. We explain the fine structu
re of the ZP lines by a dynamic Jahn-Teller distortion in the excited
state 4T1. The decay of the charge-transfer states [Fe2+ (5T2), h(b)]
leaves the Fe3+ ion in an excited state (Fe3+), which pumps the 0.5-e
V emission.