A Facile Molecular Precursor Route to Metal Phosphide Nanoparticles and Their Evaluation as Hydrodeoxygenation Catalysts

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• 作者：Susan E. Habas ; Frederick G. Baddour ; Daniel A. Ruddy ; Connor P. Nash ; Jun Wang ; Ming Pan ; Jesse E. Hensley ; Joshua A. Schaidle
• 刊名：Chemistry of Materials
• 出版年：2015
• 出版时间：November 24, 2015
• 年：2015
• 卷：27
• 期：22
• 页码：7580-7592
• 全文大小：959K
• ISSN：1520-5002

文摘

Metal phosphides have been identified as a promising class of materials for the catalytic upgrading of bio-oils, which are renewable and potentially inexpensive sources for liquid fuels. Herein, we report the facile synthesis of a series of solid, phase-pure metal phosphide nanoparticles (NPs) (Ni₂P, Rh₂P, and Pd₃P) utilizing commercially available, air-stable metal鈥損hosphine complexes in a one-pot reaction. This single-source molecular precursor route provides an alternative method to access metal phosphide NPs with controlled phases and without the formation of metal NP intermediates that can lead to hollow particles. The formation of the Ni₂P NPs was shown to proceed through an amorphous Ni鈥揚 intermediate, leading to the desired NP morphology and metal-rich phase. This low-temperature, rapid route to well-defined metal NPs is expected to have broad applicability to a variety of readily available or easily synthesized metal鈥損hosphine complexes with high decomposition temperatures. Hydrodeoxygenation of acetic acid, an abundant bio-oil component, was performed to investigate H₂ activation and deoxygenation pathways under conditions that are relevant to ex situ catalytic fast pyrolysis (high temperatures, low pressures, and near-stoichiometric H₂ concentrations). The catalytic performance of the silica-supported metal phosphide NPs was compared to the analogous incipient wetness (IW) metal and metal phosphide catalysts over the range 200鈥?00 掳C. Decarbonylation was the primary pathway for H₂ incorporation in the presence of all of the catalysts except NP-Pd₃P, which exhibited minimal productive activity, and IW-Ni, which evolved H₂. The highly controlled NP-Ni₂P and NP-Rh₂P catalysts, which were stable under these conditions, behaved comparably to the IW-metal phosphides, with a slight shift to higher product onset temperatures, likely due to the presence of surface ligands. Most importantly, the NP-Ni₂P catalyst exhibited H₂ activation and incorporation, in contrast to IW-Ni, indicating that the behavior of the metal phosphide is significantly different from that of the parent metal, and more closely resembles that of noble metal catalysts.