Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published November 18, 2019 | Supplemental Material
Journal Article Open

In-situ Nanostructuring and Stabilization of Polycrystalline Copper by an Organic Salt Additive Promotes Electrocatalytic CO₂ Reduction to Ethylene

Abstract

Bridging homogeneous molecular systems with heterogeneous catalysts is a promising approach for the development of new electrodes, combining the advantages of both approaches. In the context of CO₂ electroreduction, molecular enhancement of planar copper electrodes has enabled promising advancement towards high Faradaic efficiencies for multicarbon products. Besides, nanostructured copper electrodes have also demonstrated enhanced performance at comparatively low overpotentials. Herein, we report a novel and convenient method for nanostructuring copper electrodes using N,N'‐ethylene‐phenanthrolinium dibromide as molecular additive. Selectivities up to 70% for C≥₂ products are observed for more than 40 h without significant change in the surface morphology. Mechanistic studies reveal several roles for the organic additive, including: the formation of cube‐like nanostructures by corrosion of the copper surface, the stabilization of these nanostructures during electrocatalysis by formation of a protective organic layer, and the promotion of C≥₂ products.

Additional Information

© 2019 Wiley-‐VCH Verlag GmbH & Co. KGaA, Weinheim. Accepted manuscript online: 19 September 2019; Manuscript accepted: 19 September 2019; Manuscript revised: 13 August 2019; Manuscript received: 25 June 2019. NMR, AFM and XPS, SEM and EDX measurements were collected at the NMR Facility (Division of CCE), the Molecular Materials Research Center (Beckman Institute) and the Analytic Facilities (Division of Geological and Planetary Sciences) of the California Institute of Technology, respectively. This material is based upon work performed by the Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, supported through the Office of Science of the U.S. Department of Energy under Award Number DE-SC0004993 and Marie Curie Fellowship H2020-MSCA-IF-2017 (793471) (A.T.). J.C.P. acknowledges additional support from the Resnick Sustainability Institute at Caltech. The authors declare no conflict of interest.

Attached Files

Supplemental Material - anie201907935-s1-supportinginformation.pdf

Files

anie201907935-s1-supportinginformation.pdf
Files (5.9 MB)
Name Size Download all
md5:bd9775f19077f13494e636428c5195b1
5.9 MB Preview Download

Additional details

Created:
August 22, 2023
Modified:
October 18, 2023