Exsolution of Ru Nanoparticles on BaCe0.9Y0.1O3‐δ Modifying Geometry and Electronic Structure of Ru for Ammonia Synthesis Reaction Under Mild Conditions. Issue 6 (4th December 2022)

• Record Type: Journal Article
• Authors: Kim, Hayoung; Jan, Asif; Kwon, Deok‐Hwang; Ji, Ho‐Il; Yoon, Kyung Joong; Lee, Jong‐Ho; Jun, Yongseok; Son, Ji‐Won; Yang, Sungeun
• Is Part Of: Small. Volume 19:Issue 6(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2022-12-04
• Subjects: ammonia synthesis -- electronic structure modification -- exsolution -- geometry modification -- green ammonia -- ruthenium; Nanotechnology -- Periodicals; Nanoparticles -- Periodicals; Microtechnology -- Periodicals; 620.5
• DOI: 10.1002/smll.202205424
• Languages: English
• ISSNs: 1613-6810

Abstract

Abstract: Green ammonia is an efficient, carbon‐free energy carrier and storage medium. The ammonia synthesis using green hydrogen requires an active catalyst that operates under mild conditions. The catalytic activity can be promoted by controlling the geometry and electronic structure of the active species. An exsolution process is implemented to improve catalytic activity by modulating the geometry and electronic structure of Ru. Ru nanoparticles exsolved on a BaCe0.9 Y0.1 O3‐δ support exhibit uniform size distribution, 5.03 ± 0.91 nm, and exhibited one of the highest activities, 387.31 mmolNH3 gRu −1 h −1 (0.1 MPa and 450 °C). The role of the exsolution and BaCe0.9 Y0.1 O3‐δ support is studied by comparing the catalyst with control samples and in‐depth characterizations. The optimal nanoparticle size is maintained during the reaction, as the Ru nanoparticles prepared by exsolution are well‐anchored to the support with in‐plane epitaxy. The electronic structure of Ru is modified by unexpected in situ Ba promoter accumulation around the base of the Ru nanoparticles. Abstract : A highly active and stable ammonia synthesis catalyst is prepared by the exsolution of Ru nanoparticles from Ba1 Ce0.9 Y0.1 O3‐δ . The optimal nanoparticle size is maintained as the Ru nanoparticles are well‐anchored to the support with in‐plane epitaxy. The electronic structure of Ru is modified by in situ Ba promoter accumulation around the base of the Ru nanoparticles.