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Porous Nanocrystalline Silicon Supported Bimetallic Pd-Au Catalysts: Preparation Characterization and Direct Hydrogen Peroxide Synthesis

机译:多孔纳米晶硅负载双金属Pd-Au催化剂:制备表征和直接过氧化氢合成。

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摘要

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.
机译:首次在多孔纳米晶体硅(PSi)上制备了双金属Pd-Au催化剂。在直接过氧化氢合成的反应中测试了催化剂,并通过标准的结构和化学技术对其进行了表征。结果表明,由常规H2 [PdCl4]和H [AuCl4]前体制备的Pd-Au / PSi催化剂在氧化的PSi表面上含有单金属Pd和一系列不同的Pd-Au合金纳米颗粒。由[Pd(NH3)4] [AuCl4] 2双络合物盐(DCS)单源前体制备的PdAu2 / PSi催化剂主要包含双金属Pd-Au合金纳米颗粒。对于这两种催化剂,双金属纳米粒子的表面都富含Pd,并以Pd 0 和Pd 2 + 态包含钯。在所研究的催化剂中,PdAu2 / PSi催化剂在直接H2O2合成中最具活性和选择性,H2O2生产率​​为0.5 mol g Pd - 1 h < mo>- 1 在0.03 M H2SO 4 中的选择性为50%,H2O2浓度为0.023 M -甲醇溶液在-10°C和大气压下流过5小时后。该性能归因于H 2 O 2 合成反应中的高活性,而不良的H 2 O 2 < / sub>分解和氢化反应。 PdAu 2 / PSi催化剂的良好性能与催化剂中Pd的主要部分呈双金属Pd-Au纳米颗粒形式有关。由于多孔硅对不良副反应,高热稳定性和电导率具有惰性,高温和高压下安全操作的可能性以及完善的制造工艺,因此多孔硅被认为是直接过氧化氢合成的有希望的催化载体。

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