Preparation and Instability of Nanocrystalline Cuprous Nitride

• Published in: Inorganic chemistry Vol. 54; no. 13; pp. 6356 - 6362
• Main Authors: Reichert, Malinda D, White, Miles A, Thompson, Michelle J, Miller, Gordon J, Vela, Javier
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 06-07-2015
• Subjects: Ammonia; Colorimetry; COPPER OXIDE; CRYSTAL STRUCTURE; CUPROUS OXIDE; Decomposition; Decomposition reactions; ELECTRONIC PRODUCTS; ELECTRONIC STRUCTURE; Electronics; Instability; Nanocrystals; Nitrides
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.5b00679

Low-dimensional cuprous nitride (Cu3N) was synthesized by nitridation (ammonolysis) of cuprous oxide (Cu2O) nanocrystals using either ammonia (NH3) or urea (H2NCONH2) as the nitrogen source. The resulting nanocrystalline Cu3N spontaneously decomposes to nanocrystalline CuO in the presence of both water and oxygen from air at room temperature. Ammonia was produced in 60% chemical yield during Cu3N decomposition, as measured using the colorimetric indophenol method. Because Cu3N decomposition requires H2O and produces substoichiometric amounts of NH3, we conclude that this reaction proceeds through a complex stoichiometry that involves the concomitant release of both N2 and NH3. This is a thermodynamically unfavorable outcome, strongly indicating that H2O (and thus NH3 production) facilitate the kinetics of the reaction by lowering the energy barrier for Cu3N decomposition. The three different Cu2O, Cu3N, and CuO nanocrystalline phases were characterized by a combination of optical absorption, powder X-ray diffraction, transmission electron microscopy, and electronic density of states obtained from electronic structure calculations on the bulk solids. The relative ease of interconversion between these interesting and inexpensive materials bears possible implications for catalytic and optoelectronic applications.