Bond-centered hydrogen in silicon studied byin situdeep-level transient spectroscopy

Abstract
In situ deep level transient spectroscopy (DLTS) has been applied to investigate n-type silicon implanted with protons at low temperatures. Two DLTS signals, labeled E3 and E3, originate from hydrogen-related donor centers. The electron emission rates of the donors are similar and the two signals are discernible only because they form and anneal differently. In n-type silicon, the E3 and E3 centers transform into negatively charged centers at ∼100 K and at ≲65 K, respectively. Both signals can be regenerated at 65 K: E3 by forward-bias injection of holes and E3 by illumination with band-gap light under reverse-bias conditions. During the E3 regeneration long-range migration of hydrogen occurs, whereas E3 regenerates without migration. In the space-charge layer of reverse biased diodes, E3 converts into E3 with an activation enthalpy of 0.44 eV in oxygen-rich material, whereas E3 converts into E3 with an activation enthalpy of 0.72 eV in oxygen-poor material. It is found that the density of hydrogen sites associated with E3 approximately equals the oxygen concentration, whereas the density of E3 sites is about 1023cm3. These results provide further evidence for our previous assignment of E3 to isolated hydrogen at a bond center site and leads to the assignment of E3 to bond centered hydrogen perturbed by a nearby oxygen atom. We argue that dilated Si-Si bonds in the strain fields around impurities and defects are trapping sites for hydrogen.