The catalytic reduction of nitrites over Pt-In catalysts supported on activated carbon has been studied in a semi-batch reactor, at room temperature and atmospheric pressure, and using hydrogen as the reducing agent. The influence of the indium content on the activity and selectivity was evaluated. Monometallic Pt catalysts are very active for nitrite reduction, but the addition of up to 1 wt% of indium significantly increases the nitrogen selectivity from 0 to 96%. The decrease in the accessible noble metal surface area reduces the amount of hydrogen available at the catalyst surface, this favoring the combination of nitrogen-containing intermediate molecules to promote the formation of N instead of being deeply hydrogenated into NH. Several activated carbon-supported Pt-In catalysts, activated under different calcination and reduction temperatures, have been also evaluated in nitrite reduction. The catalyst calcined and reduced at 400°C showed the best performance considering both the activity and the selectivity to nitrogen. This enhanced selectivity is ascribed to the formation of Pt-In alloy. The electronic properties of Pt change upon alloy formation, as it is demonstrated by XPS.
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http://dx.doi.org/10.3389/fchem.2021.733881 | DOI Listing |
Nanomaterials (Basel)
November 2024
Electrochemistry Department, St. Petersburg State University, 7/9 Universitetskaya nab., 199034 St. Petersburg, Russia.
The oxygen reduction reaction (ORR) plays a central role in energy conversion and storage technologies. A promising alternative to precious metal catalysts are non-precious metal doped carbons. Considerable efforts have been devoted to cobalt-doped carbonized polyacrylonitrile catalysts, but the optimization of their catalytic performance remains a key challenge.
View Article and Find Full Text PDFPhys Chem Chem Phys
November 2024
Institute of New Energy and Low-Carbon Technology, National Engineering Research Center for Flue Gas Desulfurization, Sichuan University, Chengdu, 610207, China.
Credible property exploration or prediction can not be achieved without well-established compositions and structures of catalysts under working conditions. We construct surrogate models combination of machine learning (ML), genetic algorithm (GA) and thermodynamics (AITD) to accelerate global optimization of PtSn binary metal oxides, which are typically used for CO-assisted propane dehydrogenation to propylene. This challenging case illustrates that the subtle oxidized states of PtSnO clusters can be predicted in a large chemical space including a wide range of reaction conditions.
View Article and Find Full Text PDFTalanta
January 2025
Department of Analytical and Inorganic Chemistry, Faculty of Chemistry, University of Bialystok, K. Ciołkowskiego 1K, 15-245, Białystok, Poland.
This work presents a simple and accurate method for the fast sequential determination of Rh, Pd, and Pt in spent automotive catalysts and e-wastes using high-resolution continuum source flame atomic absorption spectrometry (HR-CS FAAS). Extensive research was carried out in model systems on the impact of potential interfering substances on analyte's signals measured in two types of flame (air-CH and NO-CH). Mutual analyte interactions were also taken into account.
View Article and Find Full Text PDFPhys Chem Chem Phys
September 2024
State Key Laboratory of Engines, Tianjin University, Tianjin 300071, China.
CO hydrogenation into valuable chemical compounds can effectively address the issues of greenhouse gas emissions and energy scarcity. The activation and dissociation processes of CO are crucial for its reduction reactions, but the effects of *H adatoms on the C-O cleavage are still confusing. This study investigates the H-assisted CO dissociation pathways on the PdPt/InO ( = 0-4) catalysts DFT calculation.
View Article and Find Full Text PDFNat Commun
August 2024
Department of Chemistry, Kay Lab of Bioorganic Phosphorus Chemistry and Chemical Biology of Ministry of Education, Beijing Key Laboratory for Analytical Methods and Instrumentation, Tsinghua University, 100084, Beijing, China.
The analysis of trace Pt single-atom (SA) represents a significant challenge, given the crucial role of single-atom platinum (Pt) in energy storage and electrocatalysis. Here, we present an electrochemiluminescence (ECL) platform that enables the qualitative and quantitative analysis of trace Pt SA using luminol as the ECL luminophore. It is observed that different Pt species in TiCT MXenes resulted in distinct reactive oxygen species (ROS) potentials for luminol cathodic electrochemiluminescence (ECL), achieved through distinctive oxygen reduction reaction (ORR) pathways, in which oxygen acts as the co-reactant.
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