Solid-solution alloying of immiscible Pt and Au boosts catalytic performance for H2O2 direct synthesis. (15th February 2021)

• Record Type: Journal Article
• Authors: Lee, Hong Woo; Nam, Hyobin; Han, Geun-Ho; Cho, Young-Hoon; Yeo, Byung Chul; Kim, Min-Cheol; Kim, Donghun; Lee, Kwan-Young; Lee, Seung Yong; Han, Sang Soo
• Is Part Of: Acta materialia. Volume 205(2021)
• Publication Date: 2021-02-15
• Subjects: Bimetallic catalyst -- Nanoparticle -- Immiscible elements -- Solid-solution alloy -- H2O2 direct synthesis; Materials -- Periodicals; Materials science -- Periodicals; Materials -- Mechanical properties -- Periodicals; Metallurgy -- Periodicals; Chemistry, Inorganic -- Periodicals; 620.112
• DOI: 10.1016/j.actamat.2020.116563
• Languages: English
• ISSNs: 1359-6454

Abstract

Abstract: Here, we propose the solid-solution alloy nanoparticles (NPs) composed of Pt and Au supported on TiO2 as an efficient catalyst for direct H2 O2 synthesis, although Pt and Au are entirely immiscible in the bulk phases. Pt and Au atoms were homogeneously distributed in a wide composition range of Ptx Au100-x NPs (10 ≤ x ≤ 80) supported on TiO2 . The most Au-rich Pt10 Au90 NPs/TiO2 exhibits the best catalytic performances, H2 O2 selectivity (94.5 ± 0.6%) and productivity (959 ± 12 mmolH2O2 gmetal −1 h −1 ), even under mild conditions (10 °C, 1 atm) and without halide-ion additives. Density functional theory calculations reveal that the introduction of inactive Au atoms strongly suppresses both O-O bond scission and OH hydrogenation, thereby enabling near unity selectivity. The Pt-Au catalyst is Pd-absent, which is noteworthy given previous efforts in direct H2 O2 synthesis are mostly limited to prototypical Pd or Pd-based modifications. This work will stimulate active utilization of immiscible elemental combinations for the direct H2 O2 synthesis catalyst development. Graphical Abstract: Image, graphical abstract