Palladium nanoparticles supported on chemically derived graphene: An efficient and reusable catalyst for the dehydrogenation of ammonia borane


Metin O., Kayhan E., ÖZKAR S., Schneider J. J.

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, cilt.37, sa.10, ss.8161-8169, 2012 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 37 Sayı: 10
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1016/j.ijhydene.2012.02.128
  • Dergi Adı: INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.8161-8169
  • Anahtar Kelimeler: Ammonia borane, Dehydrogenation, Hydrolysis, Chemically derived graphene, Palladium nanoparticles, Supported catalysts, CROSS-COUPLING REACTIONS, MONODISPERSE NICKEL NANOPARTICLES, HIGHLY-ACTIVE CATALYSTS, BORON-NITROGEN BONDS, CO-MALEIC ACID), N-H COMPOUNDS, HYDROGEN GENERATION, PD NANOPARTICLES, THERMAL-DECOMPOSITION, GRAPHITE OXIDE
  • Orta Doğu Teknik Üniversitesi Adresli: Evet

Özet

Chemically derived graphene (CDG) was prepared by hydrazine hydrate reduction of graphene oxide and used as support for palladium nanoparticles (Pd NPs) generated ex situ with controllable particle size and dispersion. The Pd NPs supported on CDG were well characterized by using a combination of advance analytical techniques and employed as catalyst in the dehydrogenation and hydrolysis of ammonia borane (AB) in organic solvents and aqueous solutions, respectively. Monodisperse Pd NPs of 4.5 nm were prepared from the reduction of palladium(II) acetylacetonate by tert-butylamine borane in the presence of oleylamine. They were readily impregnated on CDG which. has BET surface area of 500 m(2) g(-1). Pd NPs retain their particle size dispersion and stability when supported on chemically derived graphene. The resulting materials are highly active and stable catalyst for the dehydrogenation and hydrolysis of AB. In addition to their high activity and stability, these Pd NPs are also reusable catalyst in both dehydrogenation and hydrolysis of AB preserving 85% and 95% of initial activity after 5th and 10th runs, respectively. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.