Ruthenium(0) nanoparticles stabilized by metal-organic framework as an efficient electrocatalyst for borohydride oxidation reaction


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Backovic G., Sljukic B., Kanberoğlu G. S. , Yurderi M., Bulut A., Zahmakıran M. , ...Daha Fazla

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, cilt.45, ss.27056-27066, 2020 (SCI İndekslerine Giren Dergi) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 45
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1016/j.ijhydene.2020.07.034
  • Dergi Adı: INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • Sayfa Sayıları: ss.27056-27066

Özet

Described herein is a new catalytic material comprising Fe-BTC (Basolite F-300) metal-organic framework stabilized ruthenium nanoparticles (Ru@Fe-BTC) and its notable catalytic activity for the borohydride oxidation reaction (BOR). Ru@Fe-BTC catalyst was reproducibly prepared by gas-phase infiltration of Ru (cod) (cot) (cod = 1,5-cyclooctadiene and cot = 1,3,5-cyclooctatriene) precursor followed by hydrogenolysis of the inclusion compound Ru (cod) (cot)@Fe-BTC to form the Ru@Fe-BTC. The resulting catalytic material was characterized by using multi-pronged techniques and the sum of their results revealed the formation of well-dispersed, highly crystalline, and small-sized ruthenium nanoparticles (3.9 nm) within the framework of Fe-BTC by preserving its crystalline structure. Cyclic and linear scan voltammetry as well as chronoamperometry techniques were used to assess the catalytic activity and stability of Ru@Fe-BTC for BOR in strongly alkaline medium at different temperatures (25-65 degrees C) and sodium borohydride concentrations (0.01-0.12 M). The charge transfer coefficient was determined to be 0.85 and BOR at Ru@Fe-BTC was found to be a nearly first-order reaction, with the activation energy amounting to 17 kJ mol(-1). A small-scale direct borohydride/peroxide fuel cell that was assembled using Ru@Fe-BTC as an anodic catalyst delivered a maximum power density of 169 mW cm(-2) at 65 degrees C. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.