The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Double-atom catalysts as a molecular platform for heterogeneous oxygen evolution electrocatalysis
Open accessAbstract
The oxygen evolution reaction (OER) is an essential anode reaction for the generation of fuels through water splitting or CO2 electroreduction. Mixed metal oxides containing Co, Fe or Ni have proved to be the most promising OER electrocatalysts in alkaline media. However, the active sites and reaction mechanisms of these catalysts are difficult to study due to their heterogeneous nature. Here we describe a general synthesis of Co-, Fe- and Ni-containing double-atom catalysts from their single-atom precursors via in situ electrochemical transformation. Characterization reveals molecule-like bimetallic active sites for these supported catalysts. For each catalyst, we propose a catalytic cycle; all exhibit bimetallic cooperation and follow a similar O–O bond-forming step. However, the mechanisms diverge in the site and source of OH− for O–O bond formation, as well as the order of proton and electron transfer. Our work demonstrates double-atom catalysts as an attractive platform for fundamental studies of heterogeneous OER electrocatalysts. Oxygen evolution reaction (OER) catalysts often comprise multiple metal ions in various configurations, hampering mechanistic understanding of how catalysis proceeds. Now, researchers prepare a series of double-atom OER catalysts based on Ni, Fe and Co, which act as molecular-like models and are more amenable to mechanistic study.
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Cites
Electrocatalysis for the oxygen evolution reaction: recent development and future perspectives
Suen, N.-T., Hung, S.-F., Quan, Q., Zhang, N., Xu, Y.-J., & Chen, H. M. (2017) · Chemical Society Reviews · doi:10.1039/c6cs00328a · Cited by 6,307
Self-citationUniversality in Oxygen Evolution Electrocatalysis on Oxide Surfaces
Man, I. C., Su, H., Calle‐Vallejo, F., Hansen, H. A., Martínez, J. I., Inoglu, N. G., Kitchin, J., Jaramillo, T. F., Nørskov, J. K., & Rossmeisl, J. (2011) · ChemCatChem · doi:10.1002/cctc.201000397 · Cited by 4,769
Atomically dispersed Ni(i) as the active site for electrochemical CO2 reduction
Yang, H. B., Hung, S.-F., Liu, S., Yuan, K., Miao, S., Zhang, L., Huang, X., Wang, H.-Y., Cai, W., Chen, R., et al. (2018) · Nature Energy · doi:10.1038/s41560-017-0078-8 · Cited by 2,239
Self-citationFei, H., Dong, J., Feng, Y., Allen, C. S., Wan, C., Volosskiy, B., Li, M., Zhao, Z., Wang, Y., Sun, H., et al. (2018) · Nature Catalysis · doi:10.1038/s41929-017-0008-y · Cited by 1,973
The Mechanism of Water Oxidation: From Electrolysis via Homogeneous to Biological Catalysis
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Atomic cobalt on nitrogen-doped graphene for hydrogen generation
Fei, H., Dong, J., Arellano-Jiménez, M. J., Ye, G., Dong Kim, N., Samuel, E. L. G., Peng, Z., Zhu, Z., Qin, F., Bao, J., et al. (2015) · Nature Communications · doi:10.1038/ncomms9668 · Cited by 1,621
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Zhou, P., Lv, X., Tao, S., Wu, J., Wang, H., Wei, X., Wang, T., Zhou, B., Lu, Y., Frauenheim, T., et al. (2022) · Advanced Materials · doi:10.1002/adma.202204089 · Cited by 570
Boosting Oxygen Electrocatalytic Activity of Fe–N–C Catalysts by Phosphorus Incorporation
Zhou, Y., Lu, R., Tao, X., Qiu, Z., Chen, G., Yang, J., Zhao, Y., Feng, X., & Müllen, K. (2023) · Journal of the American Chemical Society · doi:10.1021/jacs.2c12933 · Cited by 567
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Gao, Y., Liu, B., & Wang, D. (2023) · Advanced Materials · doi:10.1002/adma.202209654 · Cited by 319
Boosting urea electrooxidation on oxyanion-engineered nickel sites via inhibited water oxidation
Gao, X., Bai, X., Wang, P., Jiao, Y., Davey, K., Zheng, Y., & Qiao, S.-Z. (2023) · Nature Communications · doi:10.1038/s41467-023-41588-w · Cited by 306
Metadata
- Authors
- Bai, L., Hsu, C.-S., Alexander, D. T. L., Chen, H. M., & Hu, X.
- Venue
- Nature Energy
- Published
- 2021-11-01
- Volume
- 6
- Issue
- 11
- Pages
- 1054-1066
- ISSN
- 2058-7546 (ISSN-L)
- OpenAlex
- W3208835066
- Cited by
- 328
- References
- 6
- FWCI
- 10.45
- Type
- journal article
- Language
- en
- Open access
- green
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