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Heterogeneous Catalysis01:22

Heterogeneous Catalysis

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Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

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Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
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Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide02:44

Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

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Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
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Catalysis02:50

Catalysis

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The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
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Radical Oxidation of Allylic and Benzylic Alcohols01:21

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Activated manganese(IV) oxide can selectively oxidize allylic and benzylic alcohols via a radical intermediate mechanism. Primary allylic alcohols are oxidized to aldehydes, while secondary allylic alcohols yield ketones. The redox reaction of potassium permanganate with an Mn(II) salt such as manganese sulfate (under either alkaline or acidic conditions), followed by thorough drying, yields the oxidizing agent: activated MnO2. While MnO2 is insoluble in the solvents used for the reaction, the...
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Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate02:21

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Alkenes can be dihydroxylated using potassium permanganate.  The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
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Microwave-Assisted Reactant-Protecting Strategy toward Efficient MoS2 Electrocatalysts in Hydrogen Evolution

Ning Liu1, Yulin Guo1, Xiaoyun Yang1

  • 1Department of Chemistry, Jinan University , No. 601 Huangpu Avenue West, 510632 Guangzhou, P. R. China.

ACS Applied Materials & Interfaces
|October 9, 2015
PubMed
Summary

A new microwave-assisted method uses thiourea to protect active sites in molybdenum disulfide (MoS2) nanocatalysts, significantly boosting hydrogen evolution reaction (HER) efficiency.

Keywords:
active siteshydrogen evolutionmicrowavemolybdenum disulfidereactant-protecting

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Catalysis

Background:

  • Molybdenum disulfide (MoS2) nanocatalysts are crucial for the hydrogen evolution reaction (HER).
  • High surface energy of active planes (010) and (100) leads to their disappearance during MoS2 preparation.
  • Efficient HER requires abundant exposed active sites on MoS2.

Purpose of the Study:

  • To develop a novel strategy for fabricating active-site-rich MoS2 (AS-rich MoS2) with enhanced HER performance.
  • To investigate the role of thiourea (TU) as both a reactant and capping agent in protecting active sites.
  • To elucidate the mechanism of interface engineering for high-performance nanocatalysts.

Main Methods:

  • Microwave-assisted synthesis utilizing thiourea (TU) as a reactant and capping agent.
  • Fabrication of AS-rich MoS2 through a reactant-protecting strategy.
  • Characterization of HER activity, including current density, Tafel slope, and onset overpotential.

Main Results:

  • Successfully synthesized AS-rich MoS2 with rich catalytic sites and promoted conductivity.
  • Achieved superior HER activity: high current density (68 mA cm(-2) at -300 mV vs RHE), low Tafel slope (53.5 mV dec(-1)), and low onset overpotential (180 mV).
  • Demonstrated the bifunctional role of TU in protecting and exposing active sites without additional surfactants.

Conclusions:

  • The microwave-assisted reactant-protecting strategy is a feasible and effective method for producing high-performance MoS2 nanocatalysts.
  • Interface engineering via TU protection significantly enhances MoS2 catalytic activity for HER.
  • This approach offers a promising direction for developing advanced nanocatalysts for energy applications.