Abstract
Solar fuel generation through water electrolysis or electrochemical CO2 reduction is thermodynamically limited when paired with the oxygen evolution reaction (OER). The glycerol electrooxidation reaction (GEOR) is an alternative anodic reaction with lower anodic electrochemical potential that utilizes a renewable coproduct produced during biodiesel synthesis. We show that GEOR on a Au-Pt-Bi ternary metal electrocatalyst in a model alkaline crude glycerol solution can provide significant cell potential reductions even when paired to reduction reactions in seawater and acidic catholytes via a bipolar membrane (BPM). We showed that the combination of GEOR electrooxidation and a BPM separator lowers the total cell potential by 1 V at an electrolysis current of 10.0 mA cm-2 versus to an anode performing OER when paired with hydrogen evolution and CO2 reduction cathodes. The observed voltage reduction was steady for periods of up to 80 hours, with minimal glycerol crossover observed through the membrane. These results motivate new, high-performance cell designs for photoelectrochemical solar fuels integrated systems based on glycerol electrooxidation.
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Modular solar-to-fuels electrolysis at low cell potentials enabled by glycerol electrooxidation and a bipolar membrane separator supporting information
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supporting information related to the submitted paper.
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Supporting Information
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This is the supporting information for:
Modular solar-to-fuels electrolysis at low cell potentials enabled by glycerol electrooxidation and
a bipolar membrane separator
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