Facile fabrication of poly(amidoamine) (PAMAM) dendrimers-encapsulated Ag–Co bimetallic nanoparticles for highly efficient dehydrogenation of ammonia borane. (30th January 2016)
- Record Type:
- Journal Article
- Title:
- Facile fabrication of poly(amidoamine) (PAMAM) dendrimers-encapsulated Ag–Co bimetallic nanoparticles for highly efficient dehydrogenation of ammonia borane. (30th January 2016)
- Main Title:
- Facile fabrication of poly(amidoamine) (PAMAM) dendrimers-encapsulated Ag–Co bimetallic nanoparticles for highly efficient dehydrogenation of ammonia borane
- Authors:
- Ke, Dandan
Li, Yuan
Wang, Jin
Zhang, Lu
Wang, Jidong
Zhao, Xin
Yang, Shuqin
Han, Shumin - Abstract:
- Abstract: Multifunctional poly(amidoamine) (PAMAM) dendrimers-encapsulated Ag–Co bimetallic nanoparticles (Ag–Co/PAMAM NPs) have been prepared via a facile co-complexation chemical reduction method. By exploiting the well-defined dendritic spatial construction of PAMAM dendrimers as NPs support and capping ligand, the as-synthesized NPs show unconspicuous agglomeration and uniformly distribution with average diameter of 5 nm. The Ag–Co/PAMAM NPs show the composition-dependent catalytic activity in catalytic dehydrogenation of ammonia borane (AB), with NPs in 30 atom.% Ag exhibiting the superior activity and yielding an initial turnover frequency (TOF) as high as 15.84 molH2 ·min −1 ·molM −1 . Combined with the electro–transfer interaction between Ag and Co, the effective control of the NPs dispersibility and the electro-donating ability of PAMAM dendrimers with amounts of amide and amine groups facilitate the catalytic performances of Ag–Co/PAMAM catalyst on the hydrolysis of AB. The work also includes the kinetic studies on zero-order with respect to substrate concentration and first-order reaction with respect to catalyst concentration, as well as temperature effect to determine the apparent activation energy of the reaction (Ea = 35.66 kJ mol −1 ). Furthermore, the reusability tests reveal Ag–Co/PAMAM NPs still show good catalytic activity and magnetically reusability in successive runs, which make these dendrimers-stabilized bimetallic nanoparticles promisingAbstract: Multifunctional poly(amidoamine) (PAMAM) dendrimers-encapsulated Ag–Co bimetallic nanoparticles (Ag–Co/PAMAM NPs) have been prepared via a facile co-complexation chemical reduction method. By exploiting the well-defined dendritic spatial construction of PAMAM dendrimers as NPs support and capping ligand, the as-synthesized NPs show unconspicuous agglomeration and uniformly distribution with average diameter of 5 nm. The Ag–Co/PAMAM NPs show the composition-dependent catalytic activity in catalytic dehydrogenation of ammonia borane (AB), with NPs in 30 atom.% Ag exhibiting the superior activity and yielding an initial turnover frequency (TOF) as high as 15.84 molH2 ·min −1 ·molM −1 . Combined with the electro–transfer interaction between Ag and Co, the effective control of the NPs dispersibility and the electro-donating ability of PAMAM dendrimers with amounts of amide and amine groups facilitate the catalytic performances of Ag–Co/PAMAM catalyst on the hydrolysis of AB. The work also includes the kinetic studies on zero-order with respect to substrate concentration and first-order reaction with respect to catalyst concentration, as well as temperature effect to determine the apparent activation energy of the reaction (Ea = 35.66 kJ mol −1 ). Furthermore, the reusability tests reveal Ag–Co/PAMAM NPs still show good catalytic activity and magnetically reusability in successive runs, which make these dendrimers-stabilized bimetallic nanoparticles promising heterogeneous catalysts in practical application. Graphical abstract: Highlights: A novel PAMAM dendrimers-encapsulated Ag–Co catalyst is prepared. Poly(amidoamine) dendrimers benefit AgCo NPs formation and dispersibility. Catalytic activity of AgCo/PAMAM NPs is largely enhanced on AB hydrolytic reaction. Initial turnover frequency (TOF) value reaches to 15.84 molH2 ·min −1 ·molM −1 . Synergistic effect of PAMAM-encapsulated AgCo on AB hydrolysis reaction is studied. … (more)
- Is Part Of:
- International journal of hydrogen energy. Volume 41:Number 4(2016)
- Journal:
- International journal of hydrogen energy
- Issue:
- Volume 41:Number 4(2016)
- Issue Display:
- Volume 41, Issue 4 (2016)
- Year:
- 2016
- Volume:
- 41
- Issue:
- 4
- Issue Sort Value:
- 2016-0041-0004-0000
- Page Start:
- 2564
- Page End:
- 2574
- Publication Date:
- 2016-01-30
- Subjects:
- PAMAM dendrimers -- Ag–Co bimetallic nanoparticles -- Hydrolytic dehydrogenation -- Ammonia borane
Hydrogen as fuel -- Periodicals
Hydrogène (Combustible) -- Périodiques
Hydrogen as fuel
Periodicals
665.81 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03603199 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ijhydene.2015.11.142 ↗
- Languages:
- English
- ISSNs:
- 0360-3199
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.290000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7819.xml