The relationship between electronic carriers and hydrogen migration in
a-Si:H was investigated by using secondary-ion-mass spectrometry to m
easure deuterium-diffusion profiles in the intrinsic (i) layer of p-i-
n a-Si:H photodiodes. The carrier concentration in the i layer was con
trolled by varying either the temperature, or the illumination intensi
ty, or the bias applied to the devices. It is demonstrated that hydrog
en migration in a-Si:H is controlled by an electronic mechanism, and (
i) is enhanced when the carrier population is increased by illuminatio
n and (ii) is suppressed when it is reduced below the thermal-equilibr
ium value by the application of a reverse bias to the diodes. The effe
ct is attributed to the dependence on carrier density of the dissociat
ion rate of hydrogen from Si-H bonds into the diffusion path consistin
g of interstitial sites. In addition, the migration length in the diff
usion path increases under reverse bias. The enhanced migration is ass
ociated with a decrease in the effective density of traps for hydrogen
in a carrier-depleted layer. The trap density under these conditions
is close to the dangling-bond density, suggesting that the migration l
ength is determined by capture into these defects. Possible mechanisms
for the interaction between hydrogen migration, carriers, and defects
are discussed.