Thermally stable single atom Pt/m-Al2O3 for selective hydrogenation and CO oxidation

By Zailei Zhang, Yihan Zhu, Hiroyuki Asakura, Bin Zhang, Jiaguang Zhang, Maoxiang Zhou, Yu Han, Tsunehiro Tanaka, Aiqin Wang, Tao Zhang and 1 more. Nature Communications, 2017

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Single-atom metal catalysts offer a promising way to utilize precious noble metal elements more effectively, provided that they are catalytically active and sufficiently stable. Herein, we report a synthetic strategy for Pt single-atom catalysts with outstanding stability in several reactions under demanding conditions. The Pt atoms are firmly anchored in the internal surface of mesoporous Al2O3, likely stabilized by coordinatively unsaturated pentahedral Al3+ centres. The catalyst keeps its structural integrity and excellent performance for the selective hydrogenation of 1,3-butadiene after exposure to a reductive atmosphere at 200 °C for 24 h. Compared to commercial Pt nanoparticle catalyst on Al2O3 and control samples, this system exhibits significantly enhanced stability and performance for n-hexane hydro-reforming at 550 °C for 48 h, although agglomeration of Pt single-atoms into clusters is observed after reaction. In CO oxidation, the Pt single-atom identity was fully maintained after 60 cycles between 100 and 400 °C over a one-month period. Using precious noble elements as single atom metal catalysts is highly desirable and effective. Here the authors show the use of platinum atom catalysts anchored in mesoporous Al2O3for selective hydrogenation and CO oxidation that have better stability and performance compared to their nanoparticle counterparts.

Subfields: Materials Chemistry, Mechanical Engineering, Organic Chemistry

View Paper: https://www.semanticscholar.org/paper/e2e376833b5aff1abdf1ec2065620702cd60f633