Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis

Herein, we show that group 11 CO[subscript 2] reduction catalysts are rapidly poisoned by progressive deposition of trace metal ion impurities present in high purity electrolytes. Metal impurity deposition was characterized by XPS and in situ stripping voltammetry and is coincident with loss of cata...

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Bibliographic Details
Main Authors: Wuttig, Anna (Contributor), Surendranath, Yogesh (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Chemistry (Contributor)
Format: Article
Language:English
Published: American Chemical Society (ACS), 2016-08-16T17:30:45Z.
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Online Access:Get fulltext
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100 1 0 |a Wuttig, Anna  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Chemistry  |e contributor 
100 1 0 |a Surendranath, Yogesh  |e contributor 
100 1 0 |a Wuttig, Anna  |e contributor 
100 1 0 |a Surendranath, Yogesh  |e contributor 
700 1 0 |a Surendranath, Yogesh  |e author 
245 0 0 |a Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis 
260 |b American Chemical Society (ACS),   |c 2016-08-16T17:30:45Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/103935 
520 |a Herein, we show that group 11 CO[subscript 2] reduction catalysts are rapidly poisoned by progressive deposition of trace metal ion impurities present in high purity electrolytes. Metal impurity deposition was characterized by XPS and in situ stripping voltammetry and is coincident with loss of catalytic activity and selectivity for CO[subscript 2] reduction, favoring hydrogen evolution on poisoned surfaces. Metal deposition can be suppressed by complexing trace metal ion impurities with ethylenediaminetetraacetic acid or solid-supported iminodiacetate resins. Metal ion complexation allows for reproducible, sustained catalytic activity and selectivity for CO[subscript 2] reduction on Au, Ag, and Cu electrodes. Together, this study establishes the principal mode by which group 11 CO[subscript 2] reduction catalysts are poisoned and lays out a general approach for extending the lifetime of electrocatalysts subject to impurity metal deposition. 
520 |a MIT Energy Initiative (Saudi Aramco, research agreement) 
520 |a United States. Air Force Office of Scientific Research (Award FA9550-15-1-0135) 
520 |a Massachusetts Institute of Technology. Department of Chemistry (Junior Faculty Funds) 
520 |a National Science Foundation (U.S.) (Predoctoral Fellowship) 
520 |a National Science Foundation (U.S.) (MIT MRSEC Program, award number DMR-0819762) 
546 |a en_US 
655 7 |a Article 
773 |t ACS Catalysis