ニッケル・フォスフィン複合体は,迅速かつ効率的な水素生成触媒として使用されます
Lu Gan1, Thomas L Groy, Pilarisetty Tarakeshwar
1Department of Chemistry and Biochemistry, Arizona State University , Tempe, Arizona 85287, United States.
Journal of the American Chemical Society
|January 7, 2015
まとめ
新しいニッケル複合体[Ni{\bdt}{\dppf}]は,陽子の水素への還元を効率的に触媒化する. この電気触媒は,高い活性,低過剰電位,酸性溶液における安定性を示し,水素生成の有望な経路を提供している.
科学分野:
- 無機化学 無機化学とは
- エレクトロカタリシス.
- 持続可能なエネルギー 持続可能なエネルギー
背景:
- 水素生産のための効率的な電気触媒の開発は,再生可能エネルギーにとって極めて重要です.
- ニッケル複合体は,貴金属触媒の地球に豊富な代替品としての可能性を秘めています.
研究 の 目的:
- 新型S2P2コーディネートニッケル複合体,Ni{\bdt}{\dppf}を電気触媒による陽子還元のために報告する.
- この複合体の触媒的活動,効率,安定性を調査する.
主な方法:
- 陽子の電触媒による水素への還元.
- [Ni ((bdt)) ((dppf)) ]複合体の合成と特徴付け.
- 触媒メカニズムを解明するための密度関数理論 (DFT) 計算.
主要な成果:
- [Ni(bdt) ((dppf) ]複合体は,回転頻度は1240s(-1) で,迅速かつ効率的な触媒作用を示しています.
- 低酸濃度で半活性に対して265mVの超電位を達成した.
- 酸性溶液と弱い酸による触媒で少なくとも4時間の安定性を証明した.
結論:
- 新型ニッケル複合体は,水素生産のための非常に効果的な電気触媒です.
- DFTの計算は,ニッケル中心のプロトネーションを含むメカニズムをサポートしています.
- 触媒の効率性,安定性,および弱い酸で動作する能力は,実用的な応用のための大きな可能性を示している.
さらに関連する動画
関連する概念動画
Catalysis
32.6K
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.
32.6K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
4.1K
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...
4.1K
Reduction of Alkenes: Catalytic Hydrogenation
15.3K
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...
15.3K
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
9.7K
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.
9.7K
Heterogeneous Catalysis
129
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...
129
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
6.6K
Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
6.6K


