Inorganic Materials / Electrochemistry
James L. Dye Endowed Chair
Primary Research Area
Other Area(s) of Interest
(Research Description PDF)
Hamann Group Research: There is a LOT of energy from sunlight striking the Earth’s surface: approximately 1017 Joules/second. For comparison, the averaged worldwide energy demand is approximately 1013 Joules/second. The Hamann group is engaged in interdisciplinary research to address basic science issues related to new methods and materials for utilizing this incredible resource to produce electricity and chemical fuels. Of specific interest are regenerative and non-regenerative photoelectrochemical cells, including dye-sensitized solar cells and thin-film absorber photocatalytic systems. In addition, we are interested in the use of ammonia as an energy (hydrogen) carrier and are investigating the electrocatalytic synthesis and electrolysis of ammonia.
Dye Sensitized Solar Cells: We are investigating the fundamental role of the relevant dye-sensitized solar cell, DSSC, components (redox shuttle, photoanode and sensitizer) involved in key efficiency-determining processes. Ultra-fast electron injection from a photoexcited sensitizer into a photoanode produces a charge separated state with typically high quantum efficiency. We are primarily interested in the subsequent processes of dye regeneration and recombination which control the efficiency of charge collection. We systematically vary the components involved in each reaction and interrogate them with a series of photoelectrochemical measurements. The general lessons learned will ultimately be used to develop design rules for next generation DSSCs comprised of molecules and materials which are capable of overcoming the kinetic and energetic constraints of current generation cells.
Thin Film Absorber Solar Cells: We are interested in exploring the use of thin films to overcome the problems associated with short collection length materials. One absorbing material of current interest is α-Fe2O3 (hematite). Hematite is an attractive material for solar energy conversion due to the abundance of iron in the earth’s crust, the extremely low cost, chemical stability and environmental harmlessness. In addition, hematite has been shown to be a promising water oxidation photocatalyst in a fuel-forming (non-regenerative) photoelectrochemical cells. We are currently elucidating the rate limiting steps as well as water oxidation mechanism on the electrode surface. Additional topics of recent interest include understanding the effect of substrate and underlayer materials, incorporation of dopants, and surface layers (e.g. catalysts) on the water oxidation efficiency. Additional oxide, nitride and oxynitride semiconductor materials are also under current investigation.
Ammonia Electrocatalysis: Nitrogen is the most abundant gas in Earth’s atmosphere and water is the most abundant liquid on Earth’s surface; combining the catalytic reduction of N2 with the oxidation of H2O to produce NH3 offers a route to scalable renewable energy storage. Liquid ammonia has an energy density comparable to methanol, and the stored chemical energy can in principle be used to generate electricity or H2 on demand. The electrolysis of liquid NH3 has received limited attention to date, however. We are therefore exploring the electrocatalytic conversion of liquid NH3 to H2. We are also engaged on a broader collaborative effort to develop and investigate new electro-catalysts based on earth-abundant materials for NH3 synthesis and electrolysis.
Low-Spin Cobalt(II) Redox Shuttle by Isocyanide Coordination, Raithel, A.L., Kim, T.Y., Nielsen, K., Staples, R.J., Hamann, T.W.; Sustainable Energy & Fuels 2020, 4, 2497-2507. DOI: 10.1039/D0SE00314J
Thin film photoelectrodes for solar water splitting, He, Y., Hamann, T.W., Wang, D.; Chemical Society Reviews 2019, 48, 2182–2215.
Homogeneous Electro-Catalytic Oxidation of Ammonia to N2 Under Mild Conditions, Habib-Zadeh, F., Miller, S.L., Hamann, T.W., Smith, M.R.; Proc. Nat. Acad. Sci. 2019, 116 (8) 2849–2853.
Improved Performance Induced by in-situ Ligand Exchange Reactions of Copper Bipyridyl Redox Couples in Dye-Sensitized Solar Cells, Wang, Y., Hamann, T.W.; Chem. Communic. 2018, 54, 12361–12364.
Elucidation of CuWO4 Surface States During PEC Water Oxidation, Gao, Y., Hamann, T.W.; J. Phys. Chem. Lett. 2017, 8 (12), 2700–2704.
As Precious as Platinum: Iron Nitride for Electrocatalytic Oxidation of Liquid Ammonia, Little, D.J., Edwards, D., Smith, M.R., Hamann, T.W.; ACS Appl. Mat. & Interf. 2017, 9 (19), 16228–16235.
Determination of Photoelectrochemical Water Oxidation Intermediates on a-Fe2O3 Electrode Surfaces Employing Operando ATR–IR Spectroscopy, Zandi, O., Hamann, T.W.; Nature Chemistry 2016, 8, 778–783.
B.A., 1996, Univ. of Texas
M.S., 2000, Univ. of Massachusetts
Ph.D., 2006, California Institute of Technology
Postdoctoral Fellow, Northwestern Univ. 2006-2008
|2015||SEAC Royce W. Murray Young Investigator Award|
|2013||Camille Dreyfus Teacher-Scholar Award|
|2012||Alfred P. Sloan Research Fellowship|
|2012||National Science Foundation, CAREER award|
|2011||Department of Energy, Early Career Research Program award|