Photo/electrocatalytic hydrogen peroxide production by manganese and iron porphyrin/molybdenum disulfide nanoensemblesShow others and affiliations
2022 (English)In: Small, ISSN 1613-6810, E-ISSN 1613-6829, Vol. 18, no 37, article id 2203032Article in journal (Refereed) Published
Abstract [en]
The oxygen reduction reaction (ORR) 2e− pathway provides an alternative and green route for industrial hydrogen peroxide (H2O2) production. Herein, the ORR photo/electrocatalytic activity in the alkaline electrolyte of manganese and iron porphyrin (MnP and FeP, respectively) electrostatically associated with modified 1T/2H MoS2 nanosheets is reported. The best performing catalyst, MnP/MoS2, exhibits excellent electrocatalytic performance towards selective H2O2 formation, with a low overpotential of 20 mV for the 2e− ORR pathway (Eons = 680 mV vs RHE) and an H2O2 yield up to 99%. Upon visible light irradiation, MnP/MoS2 catalyst shows significant activity enhancement along with good stability. Electrochemical impedance spectroscopy assays suggest a reduced charge transfer resistance value at the interface with the electrolyte, indicating an efficient intra-ensemble transfer process of the photo-excited electrons through the formation of a type II heterojunction or Schottky contact, and therefore justifies the boosted electrochemical activities in the presence of light. Overall, this work is expected to inspire the design of novel advanced photo/electrocatalysts, paving the way for sustainable industrial H2O2 production.
Place, publisher, year, edition, pages
John Wiley & Sons, 2022. Vol. 18, no 37, article id 2203032
Keywords [en]
hydrogen peroxide, iron, manganese, photo/electrocatalysis, porphyrins, transition metal dichalcogenides
National Category
Physical Chemistry Materials Chemistry Other Physics Topics
Identifiers
URN: urn:nbn:se:umu:diva-198917DOI: 10.1002/smll.202203032ISI: 000841646700001PubMedID: 35980982Scopus ID: 2-s2.0-85135942154OAI: oai:DiVA.org:umu-198917DiVA, id: diva2:1694434
Funder
European Social Fund (ESF), MIS‐50330212022-09-092022-09-092022-11-30Bibliographically approved