The worldwide push to generate electricity from renewable sources has created a critical need to develop improved energy storage and fuel-production strategies. Recent advances in the conversion of solar and wind energy into electrical energy have been increasingly economical, yet without effective methods for storage, it is impossible to integrate these intermittent resources into the commercial sector without compromising reliability. Research in the Matson Group focuses on using a synthetic inorganic chemistry perspective to address current global issues related to Energy Storage and Production.
An attractive solution to the broad challenge of energy storage is to store chemical energy in molecular bonds by converting inert, abundant molecules into energy-rich chemical fuels. As such, the development of new, carbon neutral fuels is a viable approach for sustainable electricity generation. The development of alternative fuels from secure and sustainable resources would decrease our dependence on fossil fuels, and as a result is among the greatest environmental and economic challenge that society faces today. The development of sustainable methods to convert energy-poor substrates to fuels requires the generation of catalysts that can perform a complex series of multi-electron and multi-proton transformations. The Matson Group is investigating new approaches to catalyst design that applies fundamental knowledge from bioinorganic systems and heterogeneous catalyst-support interactions. We have recently discovered a new class of metal-oxide metalloligands capable of participating in cooperative small molecule activation. The main objectives of this research include (i) determining how the electronic properties and activity of a homogeneous, heterometallic catalyst can be influenced by a reducible metal-oxide support and (ii) revealing the role of metal/metalloligand interactions in the cooperative intramolecular electron and proton transport that enables substrate activation. Insights from these investigations will translate broadly into improved designs for homogeneous catalysts targeting the sustainable production of chemical fuels.
Additionally, the Matson Group is developing earth-abundant, metal-oxide cluster complexes to serve as electrolytes for redox-flow batteries. Redox-flow batteries are among the most promising technologies for grid-scale energy storage. While traditional battery cells rely on internal solid electrodes for energy storage, redox flow batteries use the circulation of two soluble redox couples as electrolytes, rendering these energy storage systems highly modular and functional. In order to make redox flow batteries commercially viable, inexpensive electrolytes that provide dense electrical output must be developed. Our approach to electrolyte design capitalizes on the stability, solubility, and rich redox chemistry of the transition metal-functionalized polyoxovanadate-alkoxide clusters discovered in our laboratory. These heterometallic complexes are generated via single-step, self-assembly pathways from inexpensive, commercial starting materials and undergo multiple highly reversible redox events, making them promising candidates for flow-battery applications.
- Meyer, R. M.; Brennessel, W. W.; Love Jr., R. J.; Matson, E. M. “Synthesis of a gallium-functionalized polyoxovanadate-alkoxide cluster: Toward general routes for heterometal installation” Polyhedron, 2018, accepted article.
- Li, F.; Meyer, R.; Carpenter, S.H.; VanGelder, L.E.; Nichols, A.W.; Machan, C.W.; Neidig, M.L.; Matson, E. M. “Nitric oxide activation facilitated by the cooperative multimetallic reactivity of iron-functionalized polyoxovanadate-alkoxide clusters” Chem. Sci., 2018, 9, 6379-6389.
- Petel, B.E.; Brennessel, W.W.; Matson, E.M. “Oxygen-atom vacancy formation at polyoxovanadate-alkoxide clusters: Homogeneous models for reducible metal oxides” J. Am. Chem. Soc., 2018, 140, 8424-8428.
- VanGelder, L.E.; Matson, E.M. “Heterometal-functionalization of polyoxovanadate-alkoxides for improved performance in non-aqueous redox flow batteries” J. Mat. Chem. A, 2018, 6, 13874-13882.
- Petel, B.E.; Purak, M.; Matson, E.M. “Manganese catalyzed cross-coupling reactions of aliphatic Grignard reagents with N-heterocyclic chlorides” Synlett, 2018, DOI: 10.1055/s-0037-1610200.
- VanGelder, L.E.; Forrestel, P.L.; Brennessel, W.W.; Matson, E.M. “Site-selectivity in the halogenation of titanium-functionalized polyoxovanadate-alkoxide clusters” Chem. Comm., 2018, 54, 6839-6842 (2018 Emerging Investigators Issue).
- VanGelder, L.E.; Brennessel, W.W.; Matson, E.M. “Tuning the Redox Profiles of Polyoxovanadate-alkoxide Clusters via Heterometal Installation: Toward Designer Redox Reagents” Dalton Trans., 2018, 47, 3698-3704.
- VanGelder, L.E.; Kosswattaarachchi, A.M.; Forrestel, P.L.; Cook, T.R.; Matson E.M. “Polyoxovanadate-alkoxide Clusters as Multi-electron Charge Carriers for Symmetric Non-aqueous Redox Flow Batteries” Chem. Sci., 2018, 9, 1692-1699.
- Li, F.; Carpenter, S.H.; Higgins, R.F.; Hitt, M.G.; Brennessel, W.W.; Ferrier, M.G.; Cary, S.K.; Lezama-Pacheco, J.S.; Wright, J.T.; Stein, B.W.; Shores, M.P.; Neidig, M.L.; Kozimor, S.A.; Matson, E.M. “Polyoxovanadate-alkoxide Clusters as a Redox Reservoir for Iron” Inorg. Chem.. 2017, 56, 7065-7080.
- Li, F.; VanGelder, L.E.; Brennessel, W.W.; Matson, E.M. “Self-Assembled, Iron-Functionalized Polyoxovanadate-Alkoxide Clusters” Inorg. Chem.2016, 55, 7332-7334.
- Ford, C.L.; Park, Y.J.; Matson, E.M.; Gordon, Z.G.; Fout, A.R. “A Bioinspired Iron Catalyst for Nitrate and Perchlorate Reduciton” Science, 2016, 354, 741-743.
- Matson, E.M.; Park, Y.J.; Fout, A.R. "Nitrite Reduction in a None-Heme Iron System: Formation of an Iron(III)-Oxo" J. Am. Chem. Soc. 2014, 136, 17398-17401.