AVS 61st International Symposium & Exhibition
    Electronic Materials and Processing Monday Sessions
       Session EM-MoA

Paper EM-MoA11
Plasmonic Behavior of Copper Iron Sulfide Nanoparticles

Monday, November 10, 2014, 5:20 pm, Room 314

Session: Nanoparticles for Electronic Materials
Presenter: Katherine Plass, Franklin & Marshall College
Authors: K.E. Plass, Franklin & Marshall College
N.J. Freymeyer, Franklin & Marshall College
C. Kim, Franklin & Marshall College
C.J. Wisdo, Franklin & Marshall College
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Copper vacancies in copper chalcogenide result in sufficiently high levels of p-type doping to generate plasmon resonances. The natural tendency towards increased copper vacancies with time and air exposure is exacerbated in nanoparticles.1 We present here investigations into the stabilization of plasmonic copper sulfide-based semiconductors. Incorporation of iron slows the transition to copper deficiency2 Here we will discuss the affect of iron incorporation into copper sulfide nanoparticles on the plasmonic behavior. Various phases were produced, ranging from different polymorphs of Cu2S to CuFeS2, including solid solutions. The solid-state structure, band gaps and edges, and plasmon band absorption of these copper iron sulfide nanoparticles were responsive to the extent of iron incorporation, as investigated by powder X-ray diffraction, cyclic voltammetry, and visible/near-IR light absorption spectroscopy. The surface chemistry influences the plasmonic behavior of these copper iron sulfide nanoparticles and will be examined.3

(1) Lotfipour, M.; Machani, T.; Rossi, D. P.; Plass, K. E. Chem. Mater.2011, 23, 3032–3038.

(2) Machani, T.; Rossi, D. P.; Golden, B. J.; Jones, E. C.; Lotfipour, M.; Plass, K. E. Chem. Mater.2011, 23, 5491–5495.

(3) Freymeyer, N. J.; Cunningham, P. D.; Jones, E. C.; Golden, B. J.; Wiltrout, A. M.; Plass, K. E. Cryst. Growth Des.2013, 13, 4059–4065.