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Stabilizing a Platinum 1 Single‐Atom Catalyst on Supported Phosphomolybdic Acid without Compromising Hydrogenation Activity
Author(s) -
Zhang Bin,
Asakura Hiroyuki,
Zhang Jia,
Zhang Jiaguang,
De Sudipta,
Yan Ning
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201602801
Subject(s) - catalysis , cyclohexanol , platinum , phosphomolybdic acid , chemistry , atom (system on chip) , inorganic chemistry , nitrobenzene , hydrogen , crystallography , organic chemistry , computer science , embedded system
In coordination chemistry, catalytically active metal complexes in a zero‐ or low‐valent state often adopt four‐coordinate square‐planar or tetrahedral geometry. By applying this principle, we have developed a stable Pt 1 single‐atom catalyst with a high Pt loading (close to 1 wt %) on phosphomolybdic acid(PMA)‐modified active carbon. This was achieved by anchoring Pt on the four‐fold hollow sites on PMA. Each Pt atom is stabilized by four oxygen atoms in a distorted square‐planar geometry, with Pt slightly protruding from the oxygen planar surface. Pt is positively charged, absorbs hydrogen easily, and exhibits excellent performance in the hydrogenation of nitrobenzene and cyclohexanone. It is likely that the system described here can be extended to a number of stable SACs with superior catalytic activities.

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