Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
Porous nanocrystalline silicon supported bimetallic Pd-Au catalysts : Preparation, characterization, and direct hydrogen peroxide synthesis. / Potemkin, Dmitriy I.; Maslov, Dmitry K.; Loponov, Konstantin и др.
в: Frontiers in Chemistry, Том 6, № MAR, 85, 27.03.2018, стр. 85.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Porous nanocrystalline silicon supported bimetallic Pd-Au catalysts
T2 - Preparation, characterization, and direct hydrogen peroxide synthesis
AU - Potemkin, Dmitriy I.
AU - Maslov, Dmitry K.
AU - Loponov, Konstantin
AU - Snytnikov, Pavel V.
AU - Shubin, Yuri V.
AU - Plyusnin, Pavel E.
AU - Svintsitskiy, Dmitry A.
AU - Sobyanin, Vladimir A.
AU - Lapkin, Alexei A.
N1 - Publisher Copyright: © 2018 Potemkin, Maslov, Loponov, Snytnikov, Shubin, Plyusnin, Svintsitskiy, Sobyanin and Lapkin.
PY - 2018/3/27
Y1 - 2018/3/27
N2 - Bimetallic Pd-Au catalysts were prepared on the porous nanocrystalline silicon (PSi) for the first time. The catalysts were tested in the reaction of direct hydrogen peroxide synthesis and characterized by standard structural and chemical techniques. It was shown that the Pd-Au/PSi catalyst prepared from conventional H2[PdCl4] and H[AuCl4] precursors contains monometallic Pd and a range of different Pd-Au alloy nanoparticles over the oxidized PSi surface. The PdAu2/PSi catalyst prepared from the [Pd(NH3)4][AuCl4]2 double complex salt (DCS) single-source precursor predominantly contains bimetallic Pd-Au alloy nanoparticles. For both catalysts the surface of bimetallic nanoparticles is Pd-enriched and contains palladium in Pd0 and Pd2+ states. Among the catalysts studied, the PdAu2/PSi catalyst was the most active and selective in the direct H2O2 synthesis with H2O2 productivity of 0.5 mol gPd-1 h-1 at selectivity of 50% and H2O2 concentration of 0.023 M in 0.03 M H2SO4-methanol solution after 5 h on stream at -10°C and atmospheric pressure. This performance is due to high activity in the H2O2 synthesis reaction and low activities in the undesirable H2O2 decomposition and hydrogenation reactions. Good performance of the PdAu2/PSi catalyst was associated with the major part of Pd in the catalyst being in the form of the bimetallic Pd-Au nanoparticles. Porous silicon was concluded to be a promising catalytic support for direct hydrogen peroxide synthesis due to its inertness with respect to undesirable side reactions, high thermal stability, and conductivity, possibility of safe operation at high temperatures and pressures and a well-established manufacturing process.
AB - Bimetallic Pd-Au catalysts were prepared on the porous nanocrystalline silicon (PSi) for the first time. The catalysts were tested in the reaction of direct hydrogen peroxide synthesis and characterized by standard structural and chemical techniques. It was shown that the Pd-Au/PSi catalyst prepared from conventional H2[PdCl4] and H[AuCl4] precursors contains monometallic Pd and a range of different Pd-Au alloy nanoparticles over the oxidized PSi surface. The PdAu2/PSi catalyst prepared from the [Pd(NH3)4][AuCl4]2 double complex salt (DCS) single-source precursor predominantly contains bimetallic Pd-Au alloy nanoparticles. For both catalysts the surface of bimetallic nanoparticles is Pd-enriched and contains palladium in Pd0 and Pd2+ states. Among the catalysts studied, the PdAu2/PSi catalyst was the most active and selective in the direct H2O2 synthesis with H2O2 productivity of 0.5 mol gPd-1 h-1 at selectivity of 50% and H2O2 concentration of 0.023 M in 0.03 M H2SO4-methanol solution after 5 h on stream at -10°C and atmospheric pressure. This performance is due to high activity in the H2O2 synthesis reaction and low activities in the undesirable H2O2 decomposition and hydrogenation reactions. Good performance of the PdAu2/PSi catalyst was associated with the major part of Pd in the catalyst being in the form of the bimetallic Pd-Au nanoparticles. Porous silicon was concluded to be a promising catalytic support for direct hydrogen peroxide synthesis due to its inertness with respect to undesirable side reactions, high thermal stability, and conductivity, possibility of safe operation at high temperatures and pressures and a well-established manufacturing process.
KW - Alloy nanoparticles
KW - Bimetallic nanoparticles
KW - Direct HO synthesis
KW - Direct hydrogen peroxide synthesis
KW - Double complex salts
KW - Gold-palladium catalysts
KW - Pd-Au catalysts
KW - Porous silicon
KW - porous silicon
KW - PERFORMANCE
KW - H2O2
KW - direct hydrogen peroxide synthesis
KW - double complex salts
KW - NANOCOMPOSITES
KW - MILD CONDITIONS
KW - bimetallic nanoparticles
KW - direct H2O2 synthesis
KW - ACTIVE-SITES
KW - DECOMPOSITION
KW - gold-palladium catalysts
KW - HETEROGENEOUS CATALYSIS
KW - PREFERENTIAL CO OXIDATION
KW - OXYGEN
KW - NANOPARTICLES
KW - alloy nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=85047448289&partnerID=8YFLogxK
U2 - 10.3389/fchem.2018.00085
DO - 10.3389/fchem.2018.00085
M3 - Article
C2 - 29637068
AN - SCOPUS:85047448289
VL - 6
SP - 85
JO - Frontiers in Chemistry
JF - Frontiers in Chemistry
SN - 2296-2646
IS - MAR
M1 - 85
ER -
ID: 13593993