| Literature DB >> 32573248 |
Dominik Wielend1, Mariano Vera-Hidalgo2, Hathaichanok Seelajaroen1, Niyazi Serdar Sariciftci1, Emilio M Pérez2, Dong Ryeol Whang1,3.
Abstract
Mechanically interlocking redox-active anthraquinone onto single-walled carbon nanotubes (AQ-MINT) gives a new and advanced example of a noncovalent architecture for an electrochemical platform. Electrochemical studies of AQ-MINT as an electrode reveal enhanced electrochemical stability in both aqueous and organic solvents compared to physisorbed AQ-based electrodes. While maintaining the electrochemical properties of the parent anthraquinone molecules, we observe a stable oxygen reduction reaction to hydrogen peroxide (H2O2). Using such AQ-MINT electrodes, 7 and 2 μmol of H2O2 are produced over 8 h under basic and neutral conditions, while the control system of SWCNTs produces 2.2 and 0.5 μmol, respectively. These results reveal the potential of this rotaxane-type immobilization approach for heterogenized electrocatalysis.Entities:
Keywords: electrocatalysis; hydrogen peroxide production; immobilization; non-covalent architecture; oxygen reduction; rotaxane
Year: 2020 PMID: 32573248 DOI: 10.1021/acsami.0c06516
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229