4.6 Article

A Combined Electrochemical-Frustrated Lewis Pair Approach to Hydrogen Activation: Surface Catalytic Effects at Platinum Electrodes

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 2, Pages 900-906

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201404242

Keywords

cyclic voltammetry; electrochemistry; frustrated Lewis pairs; fuel cells; hydrogen transfer

Funding

  1. Royal Society
  2. EPSRC [EP/J500409]
  3. European Research Council under ERC [307061]
  4. European Research Council (ERC) [307061] Funding Source: European Research Council (ERC)
  5. Engineering and Physical Sciences Research Council [1093876, EP/K039946/1] Funding Source: researchfish
  6. EPSRC [EP/K039946/1] Funding Source: UKRI

Ask authors/readers for more resources

Herein, we extend our combined electrochemical-frustrated Lewis pair approach to include Pt electrode surfaces for the first time. We found that the voltammetric response of an electrochemical-frustrated Lewis pair (FLP) system involving the B(C6F5)(3)/[HB(C6F5)(3)](-) redox couple exhibits a strong surface electrocatalytic effect at Pt electrodes. Using a combination of kinetic competition studies in the presence of a H atom scavenger, 6-bromohexene, and by changing the steric bulk of the Lewis acid borane catalyst from B(C6F5)(3) to B(C6Cl5)(3), the mechanism of electrochemical-FLP reactions on Pt surfaces was shown to be dominated by hydrogen-atom transfer (HAT) between Pt, [Pt-H] adatoms and transient [HB(C6F5)(3)](center dot) electrooxidation intermediates. These findings provide further insight into this new area of combining electrochemical and FLP reactions, and proffers additional avenues for exploration beyond energy generation, such as in electrosynthesis.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available