A nanostructured hematite film prepared by a facile "top down" method for application in photoelectrochemistry. Issue 41 (20th September 2016)

• Record Type: Journal Article
• Authors: Qin, Dong-Dong; Li, Yang; Ning, Xing-Ming; Wang, Qiu-Hong; He, Cai-Hua; Quan, Jing-Jing; Chen, Jing; Li, Ying-Tao; Lu, Xiao-Quan; Tao, Chun-Lan
• Is Part Of: Dalton transactions. Volume 45:Issue 41(2016)
• Page Start: 16221
• Page End: 16230
• Publication Date: 2016-09-20
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/c6dt02809h
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Nanostructured hematite films on iron foil have been successfully prepared by using a facile "top down" method for application in photoelectrochemistry. Abstract : To overcome tough conditions currently used for the preparation of nanostructured hematite films on a conducting substrate, a rational and easy method of chemical etching involving Fe 3+ release and material growth in the presence of OH − has been developed. By carefully tuning the parameters influencing the morphologies of hematite, including the synthetic procedure, the concentration of etching solution, temperature, etching time and the morphology controlling surfactant, hematite films grown on iron foil with various morphologies ( e.g. nanorod, nanowire, ultrathin nanoflake and cauliflower-like shape) have been achieved. In particular, it is found that F − is an effective surfactant to control the morphology as well as the crystallization process of hematite. Ultrathin nanoflakes having a minimized feature size exhibit the best photocurrent of 0.5 mA cm −2 (1.23 V vs. RHE, RHE is reversible hydrogen electrode) among the samples tested as a result of facilitated hole diffusion to the electrolyte and thus lowered carrier recombination. Compared with pristine hematite, a nearly tripled photocurrent is observed when H2 O2 is added in the electrolyte as a hole scavenger, suggesting the presence of a charge injection barrier in the surface of samples. According to this, the strategy of Co 2+ treatment is utilized and the improved photocurrent is seen, likely due to the improved water oxidation kinetics and surface state passivation. We believe that this convenient and economical method can be extended to the synthesis of other alkaline metal oxide nanomaterials as long as the redox potential of S2 O8 2− /SO4 2− is higher than M n + /M (M refers to metal).