TY - JOUR
T1 - Photoinduced oxygen release and persistent photoconductivity in ZnO nanowires
AU - Bao, Jiming
AU - Shalish, Ilan
AU - Su, Zhihua
AU - Gurwitz, Ron
AU - Capasso, Federico
AU - Wang, Xiaowei
AU - Ren, Zhifeng
N1 - Funding Information:
JMB thanks Dr. Jie Xiang for help with E-beam lithography, and Mariano Zimmler and Professor Carsten Ronning for many valuable discussions. JMB also acknowledges support from TcSUH of the University of Houston and the Robert A. Welch Foundation (E-1728). I. Shalish thanks Professor Yoram Shapira for helpful discussions and acknowledges a Converging Technologies personal grant from the Israeli Science Foundation - VATAT. The work performed at Boston College is supported by DOE DE-FG02-00ER45805 (ZFR).
PY - 2011/12/1
Y1 - 2011/12/1
N2 - Photoconductivity is studied in individual ZnO nanowires. Under ultraviolet (UV) illumination, the induced photocurrents are observed to persist both in air and in vacuum. Their dependence on UV intensity in air is explained by means of photoinduced surface depletion depth decrease caused by oxygen desorption induced by photogenerated holes. The observed photoresponse is much greater in vacuum and proceeds beyond the air photoresponse at a much slower rate of increase. After reaching a maximum, it typically persists indefinitely, as long as good vacuum is maintained. Once vacuum is broken and air is let in, the photocurrent quickly decays down to the typical air-photoresponse values. The extra photoconductivity in vacuum is explained by desorption of adsorbed surface oxygen which is readily pumped out, followed by a further slower desorption of lattice oxygen, resulting in a Zn-rich surface of increased conductivity. The adsorption-desorption balance is fully recovered after the ZnO surface is exposed to air, which suggests that under UV illumination, the ZnO surface is actively "breathing" oxygen, a process that is further enhanced in nanowires by their high surface to volume ratio.
AB - Photoconductivity is studied in individual ZnO nanowires. Under ultraviolet (UV) illumination, the induced photocurrents are observed to persist both in air and in vacuum. Their dependence on UV intensity in air is explained by means of photoinduced surface depletion depth decrease caused by oxygen desorption induced by photogenerated holes. The observed photoresponse is much greater in vacuum and proceeds beyond the air photoresponse at a much slower rate of increase. After reaching a maximum, it typically persists indefinitely, as long as good vacuum is maintained. Once vacuum is broken and air is let in, the photocurrent quickly decays down to the typical air-photoresponse values. The extra photoconductivity in vacuum is explained by desorption of adsorbed surface oxygen which is readily pumped out, followed by a further slower desorption of lattice oxygen, resulting in a Zn-rich surface of increased conductivity. The adsorption-desorption balance is fully recovered after the ZnO surface is exposed to air, which suggests that under UV illumination, the ZnO surface is actively "breathing" oxygen, a process that is further enhanced in nanowires by their high surface to volume ratio.
UR - http://www.scopus.com/inward/record.url?scp=84856920980&partnerID=8YFLogxK
U2 - 10.1186/1556-276X-6-404
DO - 10.1186/1556-276X-6-404
M3 - Article
C2 - 21711938
AN - SCOPUS:84856920980
SN - 1931-7573
VL - 6
SP - 1
EP - 7
JO - Nanoscale Research Letters
JF - Nanoscale Research Letters
M1 - 404
ER -