The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.
Water Oxidation Catalysis using Amorphous Manganese Oxides, Octahedral Molecular Sieves (OMS-2), and Octahedral Layered (OL-1) Manganese Oxide Structures
Abstract
Water oxidation is the bottleneck in artificial photosynthetic systems that aim to split water into hydrogen and oxygen. However, water oxidation occurs readily in plants, catalyzed by the Mn 4 O 4 Ca manganese cluster. In addition to this, manganese minerals are ubiquitous in nature displaying layered and tunnel structures. In this study, mixed valent porous amorphous manganese oxides (AMO), along with cryptomelane type tunnel manganese oxides (OMS-2) and layered birnessite (OL-1) have been used as water oxidation catalysts. Significantly higher turnovers were obtained with AMO (290 mmol O 2 /mol Mn) compared to tunnel structure OMS-2 (110 mmol O 2 /mol Mn) and layered structure OL-1 (27 mmol O 2 /mol Mn) in water oxidation tests with Ce 4+ . Oxygen evolution was also confirmed under photochemical conditions using Ru(bpy) 3 2+ as a photosensitizer and persulfate as a sacrificial agent. The differences in catalytic activity among these catalysts have been probed using X-ray diffraction, transmission electron microscopy, Raman and Fourier transform infrared (FTIR) spectroscopy, average oxidation state, and compositional analyses. Comparison of AMO against prominent manganese catalysts described in literature shows AMO provided the highest turnover numbers. AMO catalyst was also reusable after regeneration. O-18 labeling studies proved that water was the source of dioxygen and IR proved the structural stability of AMO after reaction. AMO is related to hexagonal birnessites such as layered biogenic manganese oxides or H + -birnessite that have cation vacancies in the MnO 2 sheets rather than completely filled Mn 3+ /Mn 4+ sheets, and this is influential in catalytic activity.
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Cites
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In Situ Formation of an Oxygen-Evolving Catalyst in Neutral Water Containing Phosphate and Co 2+
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Nanostructured Cobalt Oxide Clusters in Mesoporous Silica as Efficient Oxygen‐Evolving Catalysts
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Highly Active and Robust Cp* Iridium Complexes for Catalytic Water Oxidation
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Cited by
Meng, Y., Song, W., Huang, H., Ren, Z., Chen, S.-Y., & Suib, S. L. (2014) · Journal of the American Chemical Society · doi:10.1021/ja505186m · Cited by 1,083
Self-citationRobinson, D. M., Go, Y. B., Mui, M., Gardner, G., Zhang, Z., Mastrogiovanni, D., Garfunkel, E., Li, J., Greenblatt, M., & Dismukes, G. C. (2013) · Journal of the American Chemical Society · doi:10.1021/ja310286h · Cited by 639
Ordered Mesoporous Cobalt Oxide as Highly Efficient Oxygen Evolution Catalyst
Rosen, J., Hutchings, G. S., & Jiao, F. (2013) · Journal of the American Chemical Society · doi:10.1021/ja400555q · Cited by 419
Metadata
- Authors
- Iyer, A., Del-Pilar, J., King’ondu, C. K., Kissel, E., Garces, H. F., Huang, H., El-Sawy, A. M., Dutta, P. K., & Suib, S. L.
- Venue
- The Journal of Physical Chemistry C
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-02-29
- Volume
- 116
- Issue
- 10
- Pages
- 6474-6483
- ISSN
- 1932-7447 (ISSN-L)
- 1932-7455
- OpenAlex
- W2142810237
- Cited by
- 287
- References
- 32
- FWCI
- 12.63
- Type
- journal article
- Language
- en
- Open access
- closed
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