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Selective semi-hydrogenation of acetylene is an extremely important reaction from both industrial and theoretical perspectives. Palladium, due to its unique chemical and physical properties, is the most active and currently irreplaceable metal for this reaction in industry, but the poor catalytic selectivity towards ethylene is also its inherent shortcoming. Introducing a secondary metal to tune a geometric and electronic structures of Pd nanoparticles and to create a synergistic effect is the most widely used strategy to effectively improve the overall catalytic performance of Pd-based catalysts. Thus, various supported Pd-based bimetallic catalysts for selective semi-hydrogenation of acetylene have been exploited in the past decade. Timely comparison, analysis, and summarizing of various preparation methods may offer a beneficial reference for the subsequent development of such catalysts. In this context, herein, the advances in synthesis strategies of catalysts, including nano-catalysts, single atom alloys (SAAs), as well as bimetallic dual atom catalysts are summarized systematically. Their advantages and disadvantages are comparatively discussed. Finally, future perspectives for the synthetic strategies of supported Pd-based bimetallic catalysts for selective semi-hydrogenation of acetylene are proposed.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056998 | PMC |
http://dx.doi.org/10.3390/molecules28062572 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, 116023, China.
The electrocatalytic acetylene semi-hydrogenation (EASH) driven by renewable energy offers an important non-petroleum route for ethylene production, yet suffers from insufficient reaction rate, ethylene selectivity, and energy efficiency. While tailoring catalytically active structures is effective for improving the EASH performance, the effects of mass transport at the mesoscale are poorly understood. Here, we show quantitatively the crucial role of interparticle mass transport within the catalyst layer of a gas diffusion electrode.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang, 110016, P.R. China.
The selective hydrogenation of acetylene to ethylene is a critical industrial process for purifying ethylene feedstocks. Palladium single-atom catalysts (Pd SACs) exhibit exceptional ethylene selectivity in this hydrogenation reaction. However, their isolated active sites show limited ability to capture and adsorb trace acetylene molecules from ethylene-rich streams, resulting in relatively low hydrogenation activity.
View Article and Find Full Text PDFMater Horiz
August 2025
Tianjin Key Lab for Rare Earth Materials and Applications, Center for Rare Earth and Inorganic Functional Materials, Smart Sensing Interdisciplinary Science Center, School of Materials Science and Engineering, National Institute for Advanced Materials, Nankai University, Tianjin 300350, P. R. China.
The semi-hydrogenation of ethynylbenzene is a fundamental reaction in the synthesis of polymer precursors. However, achieving a balance between catalytic activity and styrene selectivity remains a significant challenge due to the risk of over-hydrogenation. Herein, we design ternary PtCoCe rare earth alloys to synergistically regulate electronic states and adsorption geometries, thereby enhancing selective hydrogenation.
View Article and Find Full Text PDFNat Protoc
August 2025
Department of Chemistry, School of Science, Tianjin University, Tianjin, China.
The semi-hydrogenation of alkynes to alkenes, especially acetylene to ethylene, is an essential transformation that delivers raw materials and scaffolds for synthetic industries. Electrocatalytic hydrogenation, which is green and mild, provides an alternative strategy to the conventional hydrogenation process, which relies on high temperature, high pressure and flammable H. This protocol describes an electrocatalytic semi-hydrogenation method to synthesize olefins with water as the hydrogen source under ambient temperature and pressure.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Environmental Science and Engineering, School of Energy and Power Engineering, Xi'an Jiaotong University, Xi'an, 710072, China.
Electrocatalytic alkyne semi-hydrogenation (EASH) powered by renewable electricity using water as a hydrogen donor provides a sustainable alternative to conventional thermocatalysis. However, the current EASH systems predominantly follow hydrogen atom transfer (HAT) pathways, which are prone to over-hydrogenation and at the same time compete with the hydrogen evolution reaction. In this work, we report a proton-coupled electron transfer (PCET) mechanism enabled on Cu(111) surface for highly efficient and selective EASH.
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