4.7 Article

Hyper-cross-linked polymer supported rhodium: an effective catalyst for hydrogen evolution from ammonia borane

Journal

DALTON TRANSACTIONS
Volume 47, Issue 8, Pages 2561-2567

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt04549b

Keywords

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Funding

  1. Sichuan Youth Science and Technology Foundation [2016JQ0052]
  2. Opening Project of Key Laboratory of Green Chemistry of Sichuan Institutes of Higher Education [LZJ1603]
  3. Open Foundation of Key Laboratory of Sichuan Province Higher Education System [SWWT2015-2]
  4. National Natural Science Foundation of China [21777109]
  5. Scientific Research Fund of Sichuan Provincial Education Department of Sichuan Province [16TD0007]

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Metal nanoparticles (NPs) have wide applications in hydrogen evolution from ammonia-borane (AB) hydrolysis because they can provide large surface active areas for reactants, and thus produce high catalytic activity. Here, a hyper-cross-linked polymer (HCP-PPh3), which was synthesized through the Friedel-Crafts reaction of benzene and triphenylphosphine, was employed as a support to stabilize Rh NPs. The characterization results revealed that the Rh NPs were uniformly dispersed on the surface of HCP-PPh3, and that they had an average particle size of 2.1 nm. The as-prepared HCP-PPh3-Rh was used as an active catalyst for hydrogen generation from AB hydrolysis. This catalyst exhibited a high turnover frequency of 481 mol H-2 (mol(Rh) min)(-1) for AB hydrolysis under mild conditions. The high catalytic performance of HCP-PPh3-Rh can be attributed to the small size of Rh NPs and the strong interaction between the metal and HCP-PPh3. This work highlights a potentially powerful strategy for preparing highly active HCP stabilized metal NPs for AB hydrolysis to generate hydrogen.

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