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|a Wuttig, Anna
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|a Massachusetts Institute of Technology. Department of Chemistry
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|a Surendranath, Yogesh
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|a Wuttig, Anna
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|a Surendranath, Yogesh
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|a Surendranath, Yogesh
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|a Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis
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|b American Chemical Society (ACS),
|c 2016-08-16T17:30:45Z.
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|z Get fulltext
|u http://hdl.handle.net/1721.1/103935
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|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.
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|a MIT Energy Initiative (Saudi Aramco, research agreement)
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|a United States. Air Force Office of Scientific Research (Award FA9550-15-1-0135)
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|a Massachusetts Institute of Technology. Department of Chemistry (Junior Faculty Funds)
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|a National Science Foundation (U.S.) (Predoctoral Fellowship)
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|a National Science Foundation (U.S.) (MIT MRSEC Program, award number DMR-0819762)
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|a en_US
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|a Article
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|t ACS Catalysis
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