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Catalytic ammonia synthesis on HY-zeolite-supported angstrom-size molybdenum cluster.
Kamiguchi, Satoshi; Asakura, Kiyotaka; Shibayama, Tamaki; Yokaichiya, Tomoko; Ikeda, Tatsushi; Nakayama, Akira; Shimizu, Ken-Ichi; Hou, Zhaomin.
Affiliation
  • Kamiguchi S; Advanced Catalysis Research Group, RIKEN Center for Sustainable Resource Science 2-1 Hirosawa, Wako Saitama 351-0198 Japan kamigu@riken.jp.
  • Asakura K; Organometallic Chemistry Laboratory, RIKEN Cluster for Pioneering Research 2-1 Hirosawa, Wako Saitama 351-0198 Japan.
  • Shibayama T; Institute for Catalysis, Hokkaido University Sapporo 001-0021 Japan.
  • Yokaichiya T; Center for Advanced Research of Energy Conversion Materials, Hokkaido University Sapporo 060-8628 Japan.
  • Ikeda T; Department of Chemical System Engineering, Graduate School of Engineering, The University of Tokyo Tokyo 113-8656 Japan nakayama@chemsys.t.u-tokyo.ac.jp.
  • Nakayama A; Department of Chemical System Engineering, Graduate School of Engineering, The University of Tokyo Tokyo 113-8656 Japan nakayama@chemsys.t.u-tokyo.ac.jp.
  • Shimizu KI; Department of Chemical System Engineering, Graduate School of Engineering, The University of Tokyo Tokyo 113-8656 Japan nakayama@chemsys.t.u-tokyo.ac.jp.
  • Hou Z; Institute for Catalysis, Hokkaido University Sapporo 001-0021 Japan.
Chem Sci ; 15(8): 2914-2922, 2024 Feb 22.
Article in En | MEDLINE | ID: mdl-38404367
ABSTRACT
The development of new catalysts with high N2 activation ability is an effective approach for low-temperature ammonia synthesis. Herein, we report a novel angstrom-size molybdenum metal cluster catalyst for efficient ammonia synthesis. This catalyst is prepared by the impregnation of a molybdenum halide cluster complex with an octahedral Mo6 metal core on HY zeolite, followed by the removal of all the halide ligands by activation with hydrogen. In this activation, the size of the Mo6 cluster (ca. 7 Å) is almost retained. The resulting angstrom-size cluster shows catalytic activity for ammonia synthesis from N2 and H2, and the reaction proceeds continuously even at 200 °C under 5.0 MPa. DFT calculations suggest that N[triple bond, length as m-dash]N bond cleavage is promoted by the cooperation of the multiple molybdenum sites.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Sci Year: 2024 Document type: Article Country of publication: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Sci Year: 2024 Document type: Article Country of publication: Reino Unido