TY - JOUR
T1 - ZnO/BiOI heterojunction photoanodes with enhanced photoelectrochemical water oxidation activity
AU - Wang, Mingyue
AU - Kafizas, Andreas
AU - Sathasivam, Sanjayan
AU - Blunt, Matthew
AU - Moss, Benjamin
AU - Gonzalez-Carrero, Soranyel
AU - Carmalt, Claire
PY - 2023/3/21
Y1 - 2023/3/21
N2 - ZnO/BiOI heterojunction photoanode thin films were prepared by aerosol-assisted chemical vapour deposition, and the impact of growth temperature and film thickness on the water oxidation functionality was systematically investigated. A top ZnO layer with a thickness of 120 nm (deposited at 350 °C) and a 390 nm thick BiOI layer (deposited at 300 °C) were found to achieve the best photoelectrochemical performance of the heterojunction. The ZnO/BiOI heterojunction exhibited a significant increase in photoelectrochemical activity, with a photocurrent of 0.27 mA·cm−2 observed at 1.1 VRHE (350 nm, 2.58 mW·cm−2), which is ~ 2.2 times higher than that of single-layer ZnO and far higher than that of BiOI. Photoluminescence spectroscopy and transient absorption spectroscopy measurements showed that there was effective charge transfer across the heterojunction which spatially separated charge carriers and increased their lifetime and ability to drive photoelectrochemical water oxidation.
AB - ZnO/BiOI heterojunction photoanode thin films were prepared by aerosol-assisted chemical vapour deposition, and the impact of growth temperature and film thickness on the water oxidation functionality was systematically investigated. A top ZnO layer with a thickness of 120 nm (deposited at 350 °C) and a 390 nm thick BiOI layer (deposited at 300 °C) were found to achieve the best photoelectrochemical performance of the heterojunction. The ZnO/BiOI heterojunction exhibited a significant increase in photoelectrochemical activity, with a photocurrent of 0.27 mA·cm−2 observed at 1.1 VRHE (350 nm, 2.58 mW·cm−2), which is ~ 2.2 times higher than that of single-layer ZnO and far higher than that of BiOI. Photoluminescence spectroscopy and transient absorption spectroscopy measurements showed that there was effective charge transfer across the heterojunction which spatially separated charge carriers and increased their lifetime and ability to drive photoelectrochemical water oxidation.
U2 - 10.1016/j.apcatb.2023.122657
DO - 10.1016/j.apcatb.2023.122657
M3 - Article
SN - 0926-3373
VL - 331
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
M1 - 122657
ER -