Current Opinion in Chemical Engineering, Journal Year: 2023, Volume and Issue: 41, P. 100929 - 100929
Published: June 16, 2023
Language: Английский
Current Opinion in Chemical Engineering, Journal Year: 2023, Volume and Issue: 41, P. 100929 - 100929
Published: June 16, 2023
Language: Английский
Nano Research, Journal Year: 2023, Volume and Issue: 17(3), P. 2050 - 2060
Published: Nov. 18, 2023
Language: Английский
Citations
57Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 160007 - 160007
Published: Jan. 1, 2025
Language: Английский
Citations
10Nature Communications, Journal Year: 2025, Volume and Issue: 16(1)
Published: Jan. 16, 2025
Dual active sites with synergistic valence state regulation under oxidizing and reducing conditions are essential for catalytic reactions step-wise mechanisms to modulate the complex adsorption of reactant molecules on surfaces heterogeneous catalysts maximized performances, but it has been rarely explored. In this work, uniformly dispersed CuCo alloy CoO nanosheet composite dual constructed, which shows huge boost in activity catalyzing water-gas shift reaction (WGSR), a record high rate reaching 204.2 μmolCO gcat.-1 s-1 at 300 °C Cu1Co9Ox amongst reported Cu-based Co-based catalysts. A mechanism is proposed that Coδ+ species can be easily reduced by CO adsorbed Cu Co0 oxidized H2O. Systematic situ characterization results reveal addition regulate redox properties Co thus Particularly, doping Cu0 weakens affinity surface or CO2 moderate level. Moreover, also promotes oxidation *CO *COOH desorption product CO2, carbon poisoning catalyst increasing reactivity. The would provide guidance construction novel clarify its underlying reactivity enhancement induced tunning metal centers reactions.
Language: Английский
Citations
2ACS Catalysis, Journal Year: 2023, Volume and Issue: 13(7), P. 4629 - 4645
Published: March 22, 2023
Adsorption of molecules on active sites heterogeneous catalysts significantly affects their catalytic performance, which provides a perspective to understand the process/mechanism at atomic level and establish structure–function relationships. This Perspective illustrates strong correlation between adsorption reactants CeO2-based improved activity and/or selectivity for various transformations. Regulating oxygen defect CeO2 an effective approach construct two typical frustrated Lewis pair (FLP) dual-active site. Benefiting from unique spatial electronic structures, FLP exhibit "embedded" configuration small molecules, promoting activation transformation. The constructed by metal clusters vacancy could break competitive thereafter enable highly selective hydrogenations. Finally, possibilities challenges in behaviors are outlined. tailorability strength anticipated stimulate guide design high-performing catalysts.
Language: Английский
Citations
39Nature Communications, Journal Year: 2023, Volume and Issue: 14(1)
Published: Oct. 27, 2023
Dual-interfacial structure within catalysts is capable of mitigating the detrimentally completive adsorption during catalysis process, but its construction strategy and mechanism understanding remain vastly lacking. Here, a highly active dual-interfaces CeO2-x/CoO1-x/Co constructed using pronounced interfacial interaction from surrounding small CeO2-x islets, which shows high activity in catalyzing water-gas shift reaction. Kinetic evidence in-situ characterization results revealed that modulates oxidized state Co species consequently generates dual interface WGS A synergistic redox comprised independent contribution functional interfaces, including CeO2-x/CoO1-x CoO1-x/Co, authenticated by experimental theoretical results, where alleviates CO poison effect, CoO1-x/Co promotes H2 formation. The may provide guidance for fabricating dual-interfacial structures shed light on over multi-component catalyst systems.
Language: Английский
Citations
34JACS Au, Journal Year: 2023, Volume and Issue: 3(4), P. 1230 - 1240
Published: April 3, 2023
Engineering the interfacial structure between noble metals and oxides, particularly on surface of non-reducible is a challenging yet promising approach to enhancing performance heterogeneous catalysts. The interface site can alter electronic d-band metal sites, facilitating transition energy levels reacting molecules promoting reaction proceed in favorable direction. Herein, we created an active Pd-Si with tunable metal-support interaction (EMSI) by growing thin permeable silica layer oxide ZSM-5 (termed Pd@SiO2/ZSM-5). Our experimental results, combined density functional theory calculations, revealed that enhanced charge transfer from deposited Si Pd, generating electron-enriched Pd surface, which significantly lowered activation barriers for O2 H2O. resulting reactive oxygen species, including O2-, O22-, -OH, synergistically facilitated formaldehyde oxidation. Additionally, moderate promote catalytic cycle Pd0 ⇆ Pd2+, adsorption reactants. This study provides strategy design high-performance catalysts practical applications.
Language: Английский
Citations
23Molecular Catalysis, Journal Year: 2024, Volume and Issue: 558, P. 114034 - 114034
Published: March 13, 2024
Language: Английский
Citations
13Journal of Energy Chemistry, Journal Year: 2024, Volume and Issue: 91, P. 475 - 483
Published: Jan. 21, 2024
Language: Английский
Citations
12Science China Materials, Journal Year: 2024, Volume and Issue: 67(2), P. 524 - 531
Published: Jan. 23, 2024
Language: Английский
Citations
9Applied Catalysis B Environment and Energy, Journal Year: 2025, Volume and Issue: unknown, P. 125020 - 125020
Published: Jan. 1, 2025
Language: Английский
Citations
1