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Mixed-metal nanosheet water oxidation catalysts made by pulsed-laser ablation in liquids - Part 1: Synthesis, characterization, and electrocatalysis

Hunter, Bryan M. and Blakemore, James D. and Gray, Harry B. and Winkler, Jay R. and Mueller, Astrid M. (2015) Mixed-metal nanosheet water oxidation catalysts made by pulsed-laser ablation in liquids - Part 1: Synthesis, characterization, and electrocatalysis. In: 250th American Chemical Society National Meeting & Exposition, August 16-20, 2015, Boston, MA. https://resolver.caltech.edu/CaltechAUTHORS:20150918-134235578

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Abstract

Global sustainable energy solns. remain one of the greatest challenges of the 21st century. Health and climate risks assocd. with combustion of fossil fuels threaten global stability, development and national security. The sun is the most abundant and cleanest source of energy, but its intermittence on earth and unequal local energy needs require conversion into stored fuels. Chem. can meet this challenge by solar-driven water splitting with earth-abundant, efficient and robust materials. Water oxidn. is central to the prodn. of storable chem. fuels, since ample supply of cleanly, efficiently, and affordably generated protons and electrons is a prerequisite for all sustainable chem. transformations. Pulsed-laser ablation in liqs. (PLAL) is a flexible synthetic strategy to prep. earth-abundant, surfactant-free, mixed-metal (hydrous) oxide nanoparticle water oxidn. catalysts [Blakemore, Gray, Winkler, Mueller, ACS Catal. 2013, 3, 2497]. It offers size and compn. control through multiple tuneable parameters (e.g. laser pulse energy and elemental content in the ablation target and liq.). With PLAL, many different nanocatalysts can readily be synthesized and screened for water oxidn. activity, rendering PLAL a medium-throughput method for catalyst design. We prepd. a series of Ni-Fe materials and systematically varied Fe content. Oxygen evolution activity in basic electrolyte increased as Fe content decreased to 22%. Addn. of Ti^(4+) and La^(3+) ions further enhanced electrocatalysis, reaching 10 mA cm^(-2) at 260 mV overpotential; on a flat working electrode, this is the lowest overpotential to date for Fe-Ni catalysts. We spectroscopically identified [Ni-Fe]-layered double hydroxide nanosheets with intercalated nitrate and water, [Ni_(1-<i>x</i>)Fe_x(OH_2)](NO_3)_y(OH)_(x-<i>y</i>)•nH_2O, as the most active precatalyst. Higher turnover frequencies were obsd. with a greater relative proportion of a 405.1 eV N 1s (XPS binding energy) species in the nanosheets [Hunter, Blakemore, Deimund, Gray, Winkler, Mueller, J. Am. Chem. Soc. 2014, 136, 13118]. The effect of different intercalated anions on water oxidn. activity was investigated.


Item Type:Conference or Workshop Item (Paper)
Related URLs:
URLURL TypeDescription
http://www.acs.org/content/acs/en/meetings/fall-2015.htmlOrganizationConference Website
ORCID:
AuthorORCID
Hunter, Bryan M.0000-0001-8559-9304
Blakemore, James D.0000-0003-4172-7460
Gray, Harry B.0000-0002-7937-7876
Winkler, Jay R.0000-0002-4453-9716
Mueller, Astrid M.0000-0002-2785-6808
Additional Information:© 2015 American Chemical Society.
Record Number:CaltechAUTHORS:20150918-134235578
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20150918-134235578
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:60331
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:19 Sep 2015 01:17
Last Modified:09 Mar 2020 13:19

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