M
Michael R. Hoffmann
Researcher at California Institute of Technology
Publications - 522
Citations - 70877
Michael R. Hoffmann is an academic researcher from California Institute of Technology. The author has contributed to research in topics: Aqueous solution & IUCN Red List. The author has an hindex of 109, co-authored 500 publications receiving 63474 citations. Previous affiliations of Michael R. Hoffmann include Clarkson University & International Union for Conservation of Nature and Natural Resources.
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Enhanced chlorine evolution from dimensionally stable anode by heterojunction with Ti and Bi based mixed metal oxide layers prepared from nanoparticle slurry
TL;DR: In this paper, the authors reported enhanced current and energy efficiency of reactive chlorine species (RCS) generation on Ir7Ta3Oy anode by Ti/Bi mixed metal oxide heterojunction layers despite reductions in pseudo-capacitance and film conductivity.
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Lithium Dendrite Growth Control Using Local Temperature Variation
TL;DR: In this article, the authors quantified lithium dendrite growth in an optically accessible symmetric Li-metal cell, charged under imposed temperatures on the electrode surface, and found that the length measure is reduced up to 43% upon increasing anodic temperature of about 50°C.
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Soluble Sunscreens Fully Protect E. coli from Disinfection by Electrohydraulic Discharges
TL;DR: The present study confirms the existence of a significant trade-off between photon efficiency and radiative power in bacterial disinfection by UV light and shows that high-intensity radiation is able to further promote into inactive channels the lower excited state of nucleic acids responsible for DNA damage.
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Kinetics of the formation of hydroxyacetaldehyde-sulfur(IV) adducts at low pH
TL;DR: In this article, the 1,2-dihydroxy-1-ethanesulfonate (DHES) was studied spectrophotometrically over the pH range of 0.7-3.3.
Journal Article
A. J. Colussi*: Acid Dissociation versus Molecular Association of Perfluoroalkyl Oxoacids: Environmental Implications
TL;DR: Although (PFO)(2)H is held together by an exceptionally strong homonuclear covalent hydrogen bond, neither PFOS nor PFO will associate or protonate significantly at environmentally relevant subnanomolar concentrations above pH approximately 1.0.