Highly self-diffused Sn doping in α-Fe2O3 nanorod photoanodes initiated from β-FeOOH nanorod/FTO by hydrogen treatment for solar water oxidation. Issue 47 (27th November 2018)

• Record Type: Journal Article
• Authors: Ma, Haiqing; Mahadik, Mahadeo A.; Park, Jin Woo; Kumar, Manish; Chung, Hee Suk; Chae, Weon Sik; Kong, Gi Won; Lee, Hyun Hwi; Choi, Sun Hee; Jang, Jum Suk
• Is Part Of: Nanoscale. Volume 10:Issue 47(2018)
• Page Start: 22560
• Page End: 22571
• Publication Date: 2018-11-27
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c8nr07277a
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : Activation of hematite by low-temperature hydrogen reduction induced highly Sn 4+ diffusion. Abstract : In this study, we present an advanced strategy of low-temperature hydrogen annealing combined with high- temperature quenching in air for activating α-Fe2 O3 nanorod photoanodes to boost the photoelectrochemical performance. We report that various low-temperature annealing conditions (340, 360, 380, and 400 °C) under hydrogen gas flow convert β-FeOOH into magnetite (Fe3 O4 ) as well as introduce Sn 4+ diffusion from FTO substrates to its surface. Furthermore, high-temperature quenching (800 °C) resulted in the phase change of magnetite (Fe3 O4 ) into hematite (α-Fe2 O3 ) and self Sn 4+ doping into the hematite lattice. Thus, the hydrogen-assisted thermally activated hematite photoanode achieved a photocurrent density of 1.35 mA cm −2 at 1.23 V vs. RHE and 1.91 mA cm −2 at 1.4 V vs. RHE, which is 70% and 80% higher than that of directly quenched hematite at 800 °C. These combined two step strategies provide new insight into high Sn-self doping for α-Fe2 O3 photoanodes and allow for further development of more efficient solar water oxidation systems.