Issue 1, 2016

Polyethylenimine promoted electrocatalytic reduction of CO2 to CO in aqueous medium by graphene-supported amorphous molybdenum sulphide

Abstract

Efficiently and selectively converting CO2 to value-added carbon compounds remains a major challenge in sustainable energy research. In this paper, we report the synthesis of a cost-effective catalyst, i.e. amorphous molybdenum sulphide on a polyethylenimine modified reduced graphene oxide substrate, for electrocatalytically reducing CO2 into CO in CO2 saturated aqueous NaHCO3 medium with high efficiency and selectivity. The catalyst is capable of producing CO at overpotentials as low as 140 mV and reaches a maximum faradaic efficiency of 85.1% at an overpotential of 540 mV. At an overpotential of 290 mV with respect to the formation of CO, it catalyzes the formation of syngas with high stability. Detailed investigations reveal that PEI works as a co-catalyst by providing a synergetic effect with MoSx.

Graphical abstract: Polyethylenimine promoted electrocatalytic reduction of CO2 to CO in aqueous medium by graphene-supported amorphous molybdenum sulphide

Supplementary files

Article information

Article type
Paper
Submitted
17 Sep 2015
Accepted
13 Nov 2015
First published
13 Nov 2015

Energy Environ. Sci., 2016,9, 216-223

Author version available

Polyethylenimine promoted electrocatalytic reduction of CO2 to CO in aqueous medium by graphene-supported amorphous molybdenum sulphide

F. Li, S. Zhao, L. Chen, A. Khan, D. R. MacFarlane and J. Zhang, Energy Environ. Sci., 2016, 9, 216 DOI: 10.1039/C5EE02879E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements