The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Tunable Cu Enrichment Enables Designer Syngas Electrosynthesis from CO2
Open accessAbstract
Using renewable energy to recycle CO 2 provides an opportunity to both reduce net CO 2 emissions and synthesize fuels and chemical feedstocks. It is of central importance to design electrocatalysts that both are efficient and can access a tunable spectrum of products. Syngas, a mixture of carbon monoxide (CO) and hydrogen (H 2 ), is an important chemical precursor that can be converted downstream into small molecules or larger hydrocarbons by fermentation or thermochemistry. Many processes that utilize syngas require different syngas compositions: we therefore pursued the rational design of a family of electrocatalysts that can be programmed to synthesize different designer syngas ratios. We utilize in situ surface-enhanced Raman spectroscopy and first-principles density functional theory calculations to develop a systematic picture of CO* binding on Cu-enriched Au surface model systems. Insights from these model systems are then translated to nanostructured electrocatalysts, whereby controlled Cu enrichment enables tunable syngas production while maintaining current densities greater than 20 mA/cm 2 .
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Cites
Combining theory and experiment in electrocatalysis: Insights into materials design
Seh, Z. W., Kibsgaard, J., Dickens, C. F., Chorkendorff, I., Nørskov, J. K., & Jaramillo, T. F. (2017) · Science · doi:10.1126/science.aad4998 · Cited by 12,114
Enhanced electrocatalytic CO2 reduction via field-induced reagent concentration
Liu, M., Pang, Y., Zhang, B., De Luna, P., Voznyy, O., Xu, J., Zheng, X., Dinh, C. T., Fan, F., Cao, C., et al. (2016) · Nature · doi:10.1038/nature19060 · Cited by 2,000
Self-citationKim, D., Resasco, J., Yu, Y., Asiri, A. M., & Yang, P. (2014) · Nature Communications · doi:10.1038/ncomms5948 · Cited by 1,374
Self-citationSurface-Enhanced Raman Spectroscopy
Haynes, C. L., McFarland, A. D., & Van Duyne, R. P. (2005) · Analytical Chemistry · doi:10.1021/ac053456d · Cited by 1,144
Underpotential Deposition at Single Crystal Surfaces of Au, Pt, Ag and Other Materials
Herrero, E., Buller, L. J., & Abruña, H. D. (2001) · Chemical Reviews · doi:10.1021/cr9600363 · Cited by 934
Delacourt, C., Ridgway, P. L., Kerr, J. B., & Newman, J. (2008) · Journal of The Electrochemical Society · doi:10.1149/1.2801871 · Cited by 442
Electrolysis of CO2 to Syngas in Bipolar Membrane-Based Electrochemical Cells
Li, Y. C., Zhou, D., Yan, Z., Gonçalves, R. H., Salvatore, D. A., Berlinguette, C. P., & Mallouk, T. E. (2016) · ACS Energy Letters · doi:10.1021/acsenergylett.6b00475 · Cited by 313
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Cited by
Progress and perspectives of electrochemical CO2 reduction on copper in aqueous electrolyte
Nitopi, S., Bertheussen, E., Scott, S. B., Liu, X., Engstfeld, A. K., Horch, S., Seger, B., Stephens, I. E. L., Chan, K., Hahn, C., et al. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00705 · Cited by 5,223
What would it take for renewably powered electrosynthesis to displace petrochemical processes?
De Luna, P., Hahn, C., Higgins, D., Jaffer, S. A., Jaramillo, T. F., & Sargent, E. H. (2019) · Science · doi:10.1126/science.aav3506 · Cited by 3,052
Self-citationDesigning materials for electrochemical carbon dioxide recycling
Ross, M. B., De Luna, P., Li, Y., Dinh, C.-T., Kim, D., Yang, P., & Sargent, E. H. (2019) · Nature Catalysis · doi:10.1038/s41929-019-0306-7 · Cited by 1,302
Self-citationLarge-Scale and Highly Selective CO2 Electrocatalytic Reduction on Nickel Single-Atom Catalyst
Zheng, T., Jiang, K., Ta, N., Hu, Y., Zeng, J., Liu, J., & Wang, H. (2019) · Joule · doi:10.1016/j.joule.2018.10.015 · Cited by 887
Theoretical Insights into Heterogeneous (Photo)electrochemical CO2Reduction
Xu, S., & Carter, E. A. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00481 · Cited by 652
Metadata
- Authors
- Ross, M. B., Dinh, C. T., Li, Y., Kim, D., De Luna, P., Sargent, E. H., & Yang, P.
- Venue
- Journal of the American Chemical Society
- Publisher
- American Chemical Society (ACS)
- Published
- 2017-06-29
- Volume
- 139
- Issue
- 27
- Pages
- 9359-9363
- ISSN
- 0002-7863 (ISSN-L)
- 1520-5126
- OpenAlex
- W2732832598
- Cited by
- 300
- References
- 7
- FWCI
- 8.18
- Type
- journal article
- Language
- en
- Open access
- green
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