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Controlled Synthesis of PtRe and NiRe Bimetallic Catalysts for Enhanced Biomass Hydrogenation Full article

Journal Energy and Fuels
ISSN: 0887-0624 , E-ISSN: 1520-5029
Output data Year: 2024, Volume: 38, Number: 17, Pages: 16458–16472 Pages count : 15 DOI: 10.1021/acs.energyfuels.4c02475
Tags Bimetals; Catalysts; Metals; Platinum; Redox reactions; Catalyst activity; Catalyst selectivity; Coordination reactions; Extended X ray absorption fine structure spectroscopy; High resolution transmission electron microscopy; Hydrides; Hydrogen; Hydrogenation; Surface reactions; Synthesis (chemical); Transition metalsX ray absorptionX ray absorption near edge structure spectroscopyX ray photoelectron spectroscopy
Authors Kim Han Ung 1 , Makolkin Nikita Vyacheslavovich 2 , Kim Jichan 1 , Murali Vishnu 1 , Jae Jungho 1,3
Affiliations
1 School of Chemical Engineering, Pusan National University, Busan 46241, Republic of Korea
2 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, 630090, Novosibirsk, Russia
3 Institute for Environment and Energy, Pusan National University, Busan 46241, Republic of Korea

Funding (1)

1 Pusan National University

Abstract: Bimetallic catalysts of the promoted transition metal catalysts have demonstrated excellent activity and selectivity for the hydrogenation of the range of biomass-derived oxygenates to targeted deoxygenated products. The formation of well-dispersed bimetallic interfaces in the form of either low-valent rhenium coordinated to the first metals (e.g., Pt-ReOx) or alloy nanoparticles (e.g., NiRe) is key to boost the hydrogenation activity for the carboxylic acids and phenols, respectively, and the synthesis method affects the formation of these active sites. Herein, the two representative Re-based bimetallic catalysts, i.e., Pt-ReOx/TiO2 and NiRe/SiO2, for biomass hydrogenation were synthesized through controlled surface reaction (CSR), and its efficacy toward the formation of bimetallic interfacial sites compared to the traditional synthesis method, i.e., incipient wet impregnation (IWI), was demonstrated. For the CSR, the first metal was impregnated into the supporting materials and then reduced under hydrogen flow. Subsequently, Re was selectively deposited onto the reduced metal surface by the reaction of metal hydride with NH4ReO4, denoted as ex situ CSR sample. The reduction of the first metal and rhenium deposition were also performed simultaneously under hydrogen flow, denoted as an in situ sample. The synthesized catalysts were analyzed using X-ray diffraction (XRD), H2-TPR, CO chemisorption, X-ray photoelectron spectroscopy (XPS), X-ray absorption near-edge structure (XANES), extended X-ray absorption fine structure (EXAFS), and high-resolution transmission electron microscopy (HR-TEM). The catalytic properties were probed using the selective hydrogenation of acetic acid to ethanol for Pt-ReOx/TiO2 and that of 2-methoxyphenol to cyclohexane for NiRe/SiO2. We found that the in situ CSR leads to more intimate contact of two metals, allowing for the formation of the desired Pt-ReOx and NiRe interfacial sites and thereby resulting in enhanced hydrogenation activity compared to the IWI method.
Cite: Kim H.U. , Makolkin N.V. , Kim J. , Murali V. , Jae J.
Controlled Synthesis of PtRe and NiRe Bimetallic Catalysts for Enhanced Biomass Hydrogenation
Energy and Fuels. 2024. V.38. N17. P.16458–16472. DOI: 10.1021/acs.energyfuels.4c02475 WOS Scopus РИНЦ OpenAlex
Dates:
Submitted: May 24, 2024
Accepted: Jul 25, 2024
Published online: Aug 12, 2024
Published print: Sep 5, 2024
Identifiers:
Web of science: WOS:001289860600001
Scopus: 2-s2.0-85201151009
Elibrary: 73639312
OpenAlex: W4401518164
Citing: Пока нет цитирований
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