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Title: Co-feeding copper catalysts couple carbon

Journal Article · · Nature Nanotechnology
 [1];  [1]
  1. Univ. of California, Berkeley, CA (United States). Kavli Energy NanoScience Inst.; Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)

Here, the mechanistic electrochemical mass spectrometry study of ethylene production on Cu-based nanocatalysts under CO2/CO co-feeds indicates the existence of separate, reactant-specific surface adsorption sites for CO2 and CO, which guided the design of a multi-component CO2RR electrocatalyst.

Research Organization:
Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC)
Grant/Contract Number:
AC02-05CH11231
OSTI ID:
1605258
Journal Information:
Nature Nanotechnology, Vol. 14, Issue 11; ISSN 1748-3387
Publisher:
Nature Publishing GroupCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 3 works
Citation information provided by
Web of Science

References (9)

CO 2 electroreduction to ethylene via hydroxide-mediated copper catalysis at an abrupt interface journal May 2018
Evidence for product-specific active sites on oxide-derived Cu catalysts for electrochemical CO2 reduction journal December 2018
Structural Sensitivities in Bimetallic Catalysts for Electrochemical CO 2 Reduction Revealed by Ag–Cu Nanodimers journal January 2019
The path towards sustainable energy journal December 2016
Sequential catalysis controls selectivity in electrochemical CO 2 reduction on Cu journal January 2018
Designing materials for electrochemical carbon dioxide recycling journal July 2019
High-rate electroreduction of carbon monoxide to multi-carbon products journal August 2018
Mechanistic reaction pathways of enhanced ethylene yields during electroreduction of CO2–CO co-feeds on Cu and Cu-tandem electrocatalysts journal October 2019
Progress and Perspectives of Electrochemical CO 2 Reduction on Copper in Aqueous Electrolyte journal April 2019

Figures / Tables (1)