scholarly journals One-Step High-Temperature-Synthesized Single-Atom Platinum Catalyst for Efficient Selective Hydrogenation

Research ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-10 ◽  
Author(s):  
Qingyuan Bi ◽  
Xiaotao Yuan ◽  
Yue Lu ◽  
Dong Wang ◽  
Jian Huang ◽  
...  
Keyword(s):  
High Temperature ◽  
Platinum Catalyst ◽  
Arc Discharge ◽  
Utilization Efficiency ◽  
Single Atom ◽  
Excellent Thermal Stability ◽  
Sufficient Energy ◽  
Metal Support ◽  
Order Of Magnitude ◽  
One Step

Although single-atom catalysts significantly improve the atom utilization efficiency, the multistep preparation procedures are complicated and difficult to control. Herein, we demonstrate that one-step in situ synthesis of the single-atom Pt anchored in single-crystal MoC (Pt1/MoC) by using facile and controllable arc-discharge strategy under extreme conditions. The high temperature (up to 4000°C) provides the sufficient energy for atom dispersion and overall stability by forming thermodynamically favourable metal-support interactions. The high-temperature-stabilized Pt1/MoC exhibits outstanding performance and excellent thermal stability as durable catalyst for selective quinoline hydrogenation. The initial turnover frequency of 3710 h-1 is greater than those of previously reported samples by an order of magnitude under 2 MPa H2 at 100°C. The catalyst also shows broad scope activity toward hydrogenation containing unsaturated groups of C=C, C=N, and C=O. The facile, one-step, and fast arc-discharge method provides an effective avenue for single-atom catalyst fabrication that is conventionally challenging.

HASTELLOY ALLOY S

Alloy Digest ◽  
1973 ◽  
Vol 22 (1) ◽  
Keyword(s):  
Mechanical Properties ◽  
High Temperature ◽  
Heat Treating ◽  
High Temperature Alloy ◽  
Excellent Thermal Stability ◽  
Cabot Corporation ◽  
High Temperature Mechanical Properties ◽  
Temperature Performance ◽  
Resistance To Oxidation ◽  
Nickel Base

Abstract HASTELLOY alloy S is a nickel-base high-temperature alloy having excellent thermal stability, good high-temperature mechanical properties and excellent resistance to oxidation up to 2000 F. This datasheet provides information on composition, physical properties, elasticity, and tensile properties as well as creep. It also includes information on high temperature performance and corrosion resistance as well as forming, heat treating, machining, and joining. Filing Code: Ni-184. Producer or source: Stellite Division, Cabot Corporation.

scholarly journals Electronic metal–support interaction modulates single-atom platinum catalysis for hydrogen evolution reaction

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yi Shi ◽  
Zhi-Rui Ma ◽  
Yi-Ying Xiao ◽  
Yun-Chao Yin ◽  
Wen-Mao Huang ◽  
...  
Keyword(s):  
Hydrogen Evolution ◽  
Hydrogen Evolution Reaction ◽  
Structure Activity Relationship ◽  
Atomic Level ◽  
Single Atom ◽  
Activity Relationship ◽  
Support Interaction ◽  
Structure Activity ◽  
Metal Support Interaction ◽  
Metal Support

AbstractTuning metal–support interaction has been considered as an effective approach to modulate the electronic structure and catalytic activity of supported metal catalysts. At the atomic level, the understanding of the structure–activity relationship still remains obscure in heterogeneous catalysis, such as the conversion of water (alkaline) or hydronium ions (acid) to hydrogen (hydrogen evolution reaction, HER). Here, we reveal that the fine control over the oxidation states of single-atom Pt catalysts through electronic metal–support interaction significantly modulates the catalytic activities in either acidic or alkaline HER. Combined with detailed spectroscopic and electrochemical characterizations, the structure–activity relationship is established by correlating the acidic/alkaline HER activity with the average oxidation state of single-atom Pt and the Pt–H/Pt–OH interaction. This study sheds light on the atomic-level mechanistic understanding of acidic and alkaline HER, and further provides guidelines for the rational design of high-performance single-atom catalysts.

High-temperature CO2 adsorption by one-step fabricated Nd-doped Li4SiO4 pellets

2020 ◽  
pp. 128346
Author(s):  
Yuandong Yang ◽  
Shun Yao ◽  
Yingchao Hu ◽  
Jian Sun ◽  
Qiuwan Li ◽  
...  
Keyword(s):  
High Temperature ◽  
Co2 Adsorption ◽  
One Step

Design and use of an Efficient Plasma Jet Reactor for High Temperature Gas/Solid Reactions

1983 ◽  
Vol 30 ◽  
Author(s):  
F. W. Giacobbe ◽  
D. W. Schmerling
Keyword(s):  
Carbon Monoxide ◽  
High Temperature ◽  
Arc Discharge ◽  
Plasma Jet ◽  
Direct Result ◽  
Discharge Region ◽  
Plasma Flame ◽  
Powdered Carbon ◽  
High Yields ◽  
Experimental Trials

ABSTRACTA unique and efficient plasma jet reactor has been developed and used to study the high temperature production of carbon monoxide from a reaction between powdered carbon and a pure carbon dioxide plasma. The plasma jet reactor was designed to allow the injection of powdered carbon above the arc discharge region rather than into the plasma flame below the arc discharge region. High yields of carbon monoxide, produced at relatively high efficiencies, were a direct result of this technique. The plasma jet was also designed to enable rapid changing and testing of various anode insertsAverage yields of carbon monoxide in the product gases were as high as 80–87% in selected experimental trials. Carbon monoxide was produced at rates exceeding 15,000 1/hr (at STP) with a power expenditure of 52 Kw.

Laboratory soft x-ray source based on high-temperature capillary arc discharge

1991 ◽  
Author(s):  
Sergei N. Belov ◽  
Evgeny M. Golubev ◽  
Elena G. Vinokurova
Keyword(s):  
High Temperature ◽  
Arc Discharge ◽  
X Ray

scholarly journals Site-Specific Electrodeposition Enables Self-Terminating Growth of Atomically Dispersed Metal Catalysts

2020 ◽  
Author(s):  
Yi Shi ◽  
Wenmao Huang ◽  
Jian Li ◽  
Yue Zhou ◽  
Zhongqiu Li ◽  
...  
Keyword(s):  
Large Scale ◽  
Transition Metal Dichalcogenides ◽  
Metal Catalysts ◽  
Atomic Scale ◽  
Single Atom ◽  
Scale Production ◽  
Heterogenous Catalysis ◽  
Site Specific ◽  
Metal Support ◽  
Metal Dichalcogenides

<p>The growth of atomically dispersed metal catalysts (ADMCs) remains a great challenge owing to the thermodynamically driven atom aggregation. Here we report a surface-limited electrodeposition technique that uses site-specific substrates for the rapid and room-temperature synthesis of ADMCs. We obtained ADMCs by the underpotential deposition (UPD) of a single-atom nonnoble metal onto the chalcogen atoms of chemically exfoliated transition metal dichalcogenides and subsequent galvanic displacement with a more-noble single-atom metal. The site-specific electrodeposition (SSED) enables the formation of energetically favorable metal–support bonds, and then automatically terminates the sequential formation of metallic bonding. The self-terminating effect restricts the metal deposition to the atomic scale. The modulated ADMCs exhibit remarkable activity and stability in the hydrogen evolution reaction compared to state-of-the-art single-atom electrocatalysts. We demonstrate that this SSED methodology could be extended to the synthesis of a variety of ADMCs (for example, Pt, Pd, Rh, Cu, Pb, Bi, and Sn single atoms), showing its general scope for the large-scale production of functional ADMCs in heterogenous catalysis. </p>

scholarly journals Site-Specific Electrodeposition Enables Self-Terminating Growth of Atomically Dispersed Metal Catalysts

2020 ◽  
Author(s):  
Yi Shi ◽  
Wenmao Huang ◽  
Jian Li ◽  
Yue Zhou ◽  
Zhongqiu Li ◽  
...  
Keyword(s):  
Large Scale ◽  
Transition Metal Dichalcogenides ◽  
Metal Catalysts ◽  
Atomic Scale ◽  
Single Atom ◽  
Scale Production ◽  
Heterogenous Catalysis ◽  
Site Specific ◽  
Metal Support ◽  
Metal Dichalcogenides

<p>The growth of atomically dispersed metal catalysts (ADMCs) remains a great challenge owing to the thermodynamically driven atom aggregation. Here we report a surface-limited electrodeposition technique that uses site-specific substrates for the rapid and room-temperature synthesis of ADMCs. We obtained ADMCs by the underpotential deposition (UPD) of a single-atom nonnoble metal onto the chalcogen atoms of chemically exfoliated transition metal dichalcogenides and subsequent galvanic displacement with a more-noble single-atom metal. The site-specific electrodeposition (SSED) enables the formation of energetically favorable metal–support bonds, and then automatically terminates the sequential formation of metallic bonding. The self-terminating effect restricts the metal deposition to the atomic scale. The modulated ADMCs exhibit remarkable activity and stability in the hydrogen evolution reaction compared to state-of-the-art single-atom electrocatalysts. We demonstrate that this SSED methodology could be extended to the synthesis of a variety of ADMCs (for example, Pt, Pd, Rh, Cu, Pb, Bi, and Sn single atoms), showing its general scope for the large-scale production of functional ADMCs in heterogenous catalysis. </p>

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