| Literature DB >> 33105050 |
Weidong Li1,2, Yunxuan Zhao3, Yuan Liu1, Mingzi Sun4, Geoffrey I N Waterhouse5, Bolong Huang4, Kan Zhang6, Tierui Zhang3, Siyu Lu1.
Abstract
Designing bifunctional catalysts capable of driving the electrochemical hydrogen evolution reaction (HER) and also H2 evolution via the hydrolysis of hydrogen storage materials such as ammonia borane (AB) is of considerable practical importance for future hydrogen economies. Herein, we systematically examined the effect of tensile lattice strain in CoRu nanoalloys supported on carbon quantum dots (CoRu/CQDs) on hydrogen generation by HER and AB hydrolysis. By varying the Ru content, the lattice parameters and Ru-induced lattice strain in the CoRu nanoalloys could be tuned. The CoRu0.5 /CQDs catalyst with an ultra-low Ru content (1.33 wt.%) exhibited excellent catalytic activity for HER (η=18 mV at 10 mA cm-2 in 1 M KOH) and extraordinary activity for the hydrolysis of AB with a turnover frequency of 3255.4 mol ( H 2 ) mol-1 (Ru) min-1 or 814.7 mol ( H 2 ) mol-1 (cat) min-1 at 298 K, respectively, representing one of the best activities yet reported for AB hydrolysis over a ruthenium alloy catalyst. Moreover, the CoRu0.5 /CQDs catalyst displayed excellent stability during each reaction, including seven alternating cycles of HER and AB hydrolysis. Theoretical calculations revealed that the remarkable catalytic performance of CoRu0.5 /CQDs resulted from the optimal alloy electronic structure realized by incorporating small amounts of Ru, which enabled fast interfacial electron transfer to intermediates, thus benefitting H2 evolution kinetics. Results support the development of new and improved catalysts HER and AB hydrolysis.Entities:
Keywords: CoRu nanoalloys; bifunctional hydrogen production; carbon quantum dots; lattice strain
Year: 2020 PMID: 33105050 DOI: 10.1002/anie.202013985
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336