Heterostructures and quantum wells can be produced in GaInP without ch
anging the solid composition by simply varying the order parameter. Si
nce CuPt ordering reduces the band-gap energy, changes in the order pa
rameter induced by changes in growth conditions result in heterostruct
ures with band-gap energy discontinuities as large as 160 meV. The mos
t convenient growth parameter to change is the flow rate of the P prec
ursor. However, previous work has shown that under some conditions the
change in order parameter is sluggish, giving rise to graded heterost
ructures. The cause of the slow change in order parameter is the topic
of this article. CuPt ordering has been shown to be driven by the for
mation of [(1) over bar 10] P dimers, characteristic of the (2X4) surf
ace reconstruction. Thus, this study of the transient in the degree of
order induced by changing the flow rate of the P precursor has relied
on the use of surface photoabsorption (SPA) to monitor the surface re
construction during the period after the partial pressure of the P pre
cursor was reduced. The SPA transient has then been correlated with th
e abruptness of the heterostructure interface, determined from the tra
nsmission electron microscopy images and the photoluminescence spectra
, for organometallic vapor phase epitaxial (OMVPE) growth at temperatu
res of 620 and 670 degrees C using the P precursors phosphine (PH3) an
d tertiarybutylphosphine (TBP). For TBP at both 620 and 670 degrees C,
the SPA reflectance transient is extremely short, with a time constan
t of less than 10 s, corresponding to the time response of the OMVPE g
rowth system. Abrupt interfaces are produced using these conditions. F
or PH3, the SPA reflectance transient is abrupt at 670 degrees C; howe
ver, at 620 degrees C the SPA response is extremely sluggish, with a t
ime constant of approximately 6.5 min. The effect is tentatively attri
buted to a surfactant effect due to H on the surface. Corresponding he
terostructures were abrupt at 670 degrees C and graded at 620 degrees
C. (C) 1998 American Institute of Physics.