4.6 Article

Earth-Abundant Metal Pyrites (FeS2, CoS2, NiS2, and Their Alloys) for Highly Efficient Hydrogen Evolution and Polysulfide Reduction Electrocatalysis

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 118, Issue 37, Pages 21347-21356

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jp506288w

Keywords

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Funding

  1. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-FG02-09ER46664]
  2. National Science Foundation Graduate Research Fellowship Program
  3. Research Corporation for Science Advancement Scialog Award for Solar Energy Conversion
  4. University of Wisconsin-Madison H. I. Romnes Faculty Fellowship
  5. University of Wisconsin-Madison College of Engineering, Materials Research Science and Engineering Center [NSF DMR-1121288]
  6. Nanoscale Science and Engineering Center [NSF DMR-0832760]
  7. Division Of Materials Research
  8. Direct For Mathematical & Physical Scien [0832760] Funding Source: National Science Foundation

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Many materials have been explored as potential hydrogen evolution reaction (HER) electrocatalysts to generate clean hydrogen fuel via water electrolysis, but none so far compete with the highly efficient and stable (but cost prohibitive) noble metals. Similarly, noble metals often excel as electrocatalytic counter electrode materials in regenerative liquid-junction photoelectrochemical solar cells, such as quantum dot-sensitized solar cells (QDSSCs) that employ the sulfide/polysulfide redox electrolyte as the hole mediator. Here, we systematically investigate thin films of the earth-abundant pyrite-phase transition metal disulfides (FeS2, CoS2, NiS2, and their alloys) as promising alternative electrocatalysts for both the HER and polysulfide reduction. Their electrocatalytic activity toward the HER is correlated to their composition and morphology. The emergent trends in their performance suggest that cobalt plays an important role in facilitating the HER, with CoS2 exhibiting highest overall performance. Additionally, we demonstrate the high activity of the transition metal pyrites toward polysulfide reduction and highlight the particularly high intrinsic activity of NiS2, which could enable improved QDSSC performance. Furthermore, structural disorder introduced by alloying different transition metal pyrites could increase their areal density of active sites for catalysis, leading to enhanced performance.

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