Page 14 - Book of Abstracts
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th
                               8  Biannual Conference on Chemistry - CHEM 08





                           Promising Formic Acid Electro-oxidation at Ferric

                     Oxyhydroxide Nanoparticles-modified Platinum   Surfaces


                    Bilquis Ali Al-Qodami , Hafsa H. Alalawya, Sayed Y. Sayed , Nageh K.
                                                                                      1
                                             1
                                         Allam , Ahmad M. Mohammad *
                                                                           1
                                                2
                                  Corresponding author: Bilquisali2015@hotmail.com

                                                     ABSTRACT

                    Direct formic acid fuel cells (DFAFCs) have attracted significant attention
                    due to their low fuel crossover, high work concentration and high energy
                    density (2086 wh L ), In addition, it has demonstrated superiority over the
                                        -1
                    long-investigated  hydrogen  fuel  cells  (HFCs)  and  direct  methanol  fuel
                    cells (DMFCs) in providing electricity to portable electronic devices. This
                    was  mainly  estimated  from  its  relatively  high  theoretical  open-circuit
                    potential (1.45 V), while the theoretical open-circuit potential for HFCs
                    and DMFCs are 1.23 and 1.21 V respectively. To ensure a rapid marketing
                    for DFAFCs, a facile synthesis of a binary FeOOH/Pt nanoanode for formic
                    acid electro-oxidation (FAO) was achieved. The investigation confirmed
                    the substrate’s dependence of FAO where a Pt surface was necessary but
                    gold  (Au),  glassy  carbon  (GC),  and  nano-FeOOH  surfaces  showed  a
                    complete inertness. Interestingly, with this simple modification of Pt with
                    nano-FeOOH followed by a post-activation process (at -0.5 V vs. Ag/AgCl
                    in  0.2  mol  L-1 NaOH)  the  effectiveness  of  Pt  toward  FAO  increased
                    significantly.  Field-emission  scanning  electron  microscopy  (FE-SEM),
                    energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD)
                    were all employed to inspect, respectively, the surface morphology, bulk
                    composition  and  crystal  structure  of  the  catalyst.  The  electrochemical
                    impedance spectra could correlate the charge transfer resistances for FAO
                    over  the  inspected  set  of  catalysts  to  explore  the  role  of  FeOOH  in
                    mediating the reaction mechanism.











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