Abstract
We report the photoelectrochemical (PEC) performance of a densely grown single crystalline hematite (α-Fe(2)O(3)) nanosheet photoanode for water splitting. Unlike expensive ITO/FTO substrates, the sheets were grown on a piece of pure Fe through controlled thermal oxidation, which is a facile low cost and one-step synthesis route. The sheets grow with a widest surface parallel to basal plane (0001). Iron oxide formed on Fe consisting of layer structure α-Fe(2)O(3)-Fe(3)O(4)-Fe is elucidated from GIXRD and correlated to spectral features observed in Raman and UV-vis spectroscopy. The top α-Fe(2)O(3) nanosheet layer serves as a photoanode, whereas the conducting Fe(3)O(4) layer serves to transport photogenerated electrons to the counter electrode through its back contact. Time-resolved photoluminescence (TRPL) measurements revealed significantly prolonged carrier lifetime compared to that of bulk. Compared to the thin film of α-Fe(2)O(3) grown on the FTO substrate, ∼3 times higher photocurrent density (0.33 mA cm(-2) at 1.23 V(RHE)) was achieved in the nanosheet sample under solar simulated AM 1.5 G illumination. The sample shows a bandgap of 2.1 eV and n-type conductivity with carrier density 9.59 × 10(17) cm(-3). Electrochemical impedance spectroscopy (EIS) measurements reveal enhanced charge transport properties. The results suggest that nanosheets synthesized by the simple method yield far better PEC performance than the thin film on the FTO substrate. The anodic shifts of flat band potential, delayed electron-hole recombination, and growth direction parallel to the highly conducting basal plane (0001) being some of the contributing factors to the higher photocurrent observed in the NS photoanode are discussed. Characterizations carried out before and after the PEC reaction show excellent stability of the nanosheets in an alkaline electrochemical environment.