安定した低温 H2生成触媒は,α-MoC に Pt を混ぜて生成する
Xiao Zhang1,2, Mengtao Zhang1, Yuchen Deng1
1Beijing National Laboratory for Molecular Sciences, College of Chemistry and Molecular Engineering and College of Engineering, and BIC-ESAT, Peking University, Beijing, China.
Nature
|January 21, 2021
まとめ
低温で水とガスのシフト反応で 効率的に水素を生成する 新しいプラチナ触媒を開発しました この耐久性の高い触媒は 清潔なエネルギーの生産に 有望な経路を提供します
科学分野:
- カタリシス
- 材料科学
- エネルギー生産
背景:
- 水ガスシフト反応は,工業用水素生産に不可欠です.
- 低温での効率的なWGS触媒は燃料電池の用途に不可欠です.
- 既存の触媒は低温で必要な耐久性と活性性に欠けていることが多い.
研究 の 目的:
- 低温でのWGS反応のための高度に活性で安定した触媒を開発する.
- モリブデン炭化物のプラチナ原子とクラスターを含む新しい触媒構造を調査する.
- 反応機構を理解し,触媒の安定に寄与する要因を特定する.
主な方法:
- 単離プラチナ原子 (Pt1) と亜ナノメートルプラチナクラスター (Ptn) をα-モリブデン炭化物 (α-MoC) に安定させる (Pt1-Ptn) /α-MoC触媒構造の合成.
- ケルビン313で WGS反応で触媒の性能をテストする.
- 直接の一酸化炭素解離を含む,触媒構造の特徴と水素生成経路の識別.
主要な成果:
- (Pt1-Ptn) /α-MoC触媒は,313 KでWGS反応に高い活性を示した.
- 直接的な一酸化炭素解離を含む水素生成経路が特定された.
- 触媒は,サポート酸化を防ぐために高い安定性を示し,4,300,000mol H2/mol Ptの高い金属正常化回転数を達成した.
結論:
- 孤立したプラチナ原子とクラスタをα-モリブデン炭化物で安定させることは,活性で安定したWGS触媒を開発するための重要な戦略です.
- 設計された触媒は,以前のシステムの限界を克服し,優れた性能と耐久性を示しています.
- このアプローチは,効率的な水と一酸化炭素の活性化によるエネルギー生産のための高度な触媒の設計に不可欠であると予想されています.
関連する概念動画
Reduction of Alkenes: Catalytic Hydrogenation
13.3K
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
13.3K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.7K
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...
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...
3.7K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
8.5K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
8.5K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
19.8K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
19.8K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
11.7K
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.
11.7K
Catalysis
29.1K
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.
29.1K


