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Cited by 287

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis

Open access
Wuttig, Anna, Surendranath, Yogesh·2015·ACS Catalysis

Abstract

Herein, we show that group 11 CO 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 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 2 reduction on Au, Ag, and Cu electrodes. Together, this study establishes the principal mode by which group 11 CO 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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Crossref · 10.1021/acscatal.5b00808

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Metadata

Authors
Wuttig, A., & Surendranath, Y.
Venue
ACS Catalysis
Published
2015-06-24
Volume
5
Issue
7
Pages
4479-4484
ISSN
2155-5435 (ISSN-L)
OpenAlex
W2515773792
Cited by
287
References
7
FWCI
5.87
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis. https://app.cochat.ai/papers/10.1021/acscatal.5b00808
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Wuttig, A., & Surendranath, Y. (2015). Impurity Ion Complexation Enhances Carbon Dioxide Reduction Catalysis. ACS Catalysis. https://doi.org/10.1021/acscatal.5b00808

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.