Photoelectrochemical water splitting at low applied potential using a NiOOH coated codoped (Sn, Zr) α-Fe₂O₃ photoanode
2015
Tamirat, Andebet Gedamu | Su, Wei-Nien | Dubale, Amare Aregahegn | Chen, Hung-Ming | Hwang, Bing-Joe
One of the major challenges in photoelectrochemical water splitting is to develop an efficient photoanode that can oxidize water at low applied potential. Herein, a codoped (Sn, Zr) α-Fe₂O₃ photoanode modified with a stable and earth abundant nickel oxyhydroxide (NiOOH) co-catalyst that can split water at low applied potential is reported. First, an unintentional gradient monodoped (Sn) α-Fe₂O₃ photoanode was synthesized at controlled annealing temperature that achieved a photocurrent density of 0.86 mA cm⁻² at 1.23 V vs. RHE. Further doping with an optimized amount of Zr outperformed the monodoped (Sn) α-Fe₂O₃ photoanode providing significantly much higher photocurrent density (1.34 mA cm⁻²). The remarkably improved electrical conductivity and more than three times higher charge carrier density (as evidenced from electrochemical impedance spectroscopy measurements and Mott–Schottky analysis) of the codoped (Sn, Zr) α-Fe₂O₃ photoanode highlight the importance of codoping. The synergetic effect of codoping (Sn, Zr) led to 1.6-fold enhancement in charge separation efficiency at 1.23 V compared to the monodoped (Sn) α-Fe₂O₃ photoanode. The NiOOH modified codoped (Sn, Zr) α-Fe₂O₃ photoanode exhibited drastically lower onset potential (0.58 V) and a photocurrent density of 1.64 mA cm⁻² at 1.23 V. Interestingly a 160 mV cathodic shift in photocurrent onset potential was also observed. Concomitant with this, the NiOOH modified codoped (Sn, Zr) α-Fe₂O₃ photoanode exhibited 1.6 to 9.5-fold enhancement in charge injection efficiency (ηᵢₙⱼ) at the kinetic control region of 0.7 to 0.9 V compared to the unmodified codoped photoanode. Gas evolution measurements also showed that the NiOOH modified codoped α-Fe₂O₃ photoanode achieved an average Faradaic efficiency of 93%.
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