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Enhanced Oxygen Evolution Reaction Activity of LaFeO3 with Co-Pi Decoration

Tuesday, 7 October 2014
Expo Center, 1st Floor, Center and Right Foyers (Moon Palace Resort)
Q. Peng (State Key Laboratory of Digital Manufacturing Equipment and Technology, School of Mechanical Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, Hubei, People’s Republic of China), Y. Wen (State Key Laboratory of Material Processing and Die &Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan 430074, Hubei, People’s Republic of China), B. Shan, and R. Chen (Huazhong University of Science and Technology)
With the continuing energy demand and environmental deterioration by conventional coal and gasoline, it is urgent to develop renewable energy. Among many methods, water splitting to generate clean hydrogen fuels is among the most promising one. Many perovskites such as SrTiO3, NaTaO3 and AgNbO3 have become candidates materials for water splitting due to their high catalytic activity and flexible structures. However, the H2 production efficiency is relatively low at visible light regime because of the large band gap of most perovskite materials. From the view point of optical absorption, LaFeO3 with a band gap of 2.07eV [1] shall be a good candidate. Nonetheless, the poor oxygen evolution reaction (OER) performance of LaFeO3severely limits its water-splitting efficiency. To solve the problem, OER improvement is needed.

RuO2, IrO2 and Pt are the conventional OER catalyst [2-3], but they are of high cost. Co-Pi, an amorphous cobalt-phosphate-based material, is reported having a low over potential for OER in the phosphate buffer solution at pH 7~8[4] and its coating on hematite promotes the photoelecrochemistry performance effectively [5]. We report here the combination of the low cost Co-Pi with LaFeO3 to enhance the OER activity of LaFeO3. We demonstrate that an effective negative shift of 100meV for the onset potential with Co-Pi coating as OER improvement. The photoelectrochemical properties and its mechanism will also be discussed.

References:

  1. K.M. Parida, Inter. J. of Hydrogen Energy, 35, 12161~12168 (2010).
  2. E. Tsuji, A. Imanishi, K. I. Fukui, Y. Nakato, Electrochim.Acta, 56, 2009 (2011).
  3. L. Ouattara, S. Fierro, O. Frey, M Koudelka, C. Comninellis, J. Appl. Electrochem, 39, 1361 (2009).
  4. M. W. Kanan, D. G. Nocera, Science, 321, 1072–1075, 2008.
  5. D. K. Zhong, D. R. Gamelin, J. Am. Chem. Soc, 131, 6086–6087, 2009.