Tsuji Ryuki, Koshino Yuuki, Masutani Hideaki, Haruyama Yuichi, Niibe Masahito, Suzuki Satoru, Nakashima Seiji, Fujisawa Hironori, Ito Seigo
Department of Materials and Synchrotron Radiation Engineering, Graduate School of Engineering, University of Hyogo, 2167 Shosha, Himeji, Hyogo 671-2280, Japan.
Laboratory of Advanced Science and Technology for Industry, University of Hyogo, 3-1-2 Kouto, Ako, Hyogo 678-1205, Japan.
ACS Omega. 2020 Mar 12;5(11):6090-6099. doi: 10.1021/acsomega.0c00074. eCollection 2020 Mar 24.
An inexpensive, simple, and high-activity catalyst preparation method has been introduced in this work. Pt and RuO catalysts were fabricated by soaking inexpensive graphite electrodes (pencil-lead graphite rod: PGR) in catalyst precursor solutions and using a simple flame-annealing method, which results in lower amount of Pt and RuO catalyst layers. From X-ray photoelectron spectroscopy and near-edge X-ray absorption fine structure analysis, it has been found that platinum and ruthenium were deposited as zero-valence metal (Pt) and oxide (RuO ), respectively. Catalytic activities of Pt/PGR and RuO /PGR for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) were evaluated using neutral 1 M NaSO aqueous electrolyte, respectively. Although HER and OER currents using PGR without catalysts were -16 mA cm (at -1.5 V vs Ag/AgCl) and +20 mA cm (at +2.0 V vs Ag/AgCl), they were improved to -110 and +80 mA cm with catalysts (Pt and RuO ), respectively. Such an inexpensive and rapid catalyst electrode preparation method on PGR using flame-annealing is a very significant method in the initial catalyst activity evaluation requiring a large amount of trial and error.