Issue 21, 2015

Rapid direct conversion of Cu2−xSe to CuAgSe nanoplatelets via ion exchange reactions at room temperature

Abstract

The use of template nanostructures for the creation of photovoltaic and thermoelectric semiconductors is becoming a quickly expanding synthesis strategy. In this work we report a simple two-step process enabling the formation of ternary CuAgSe nanoplatelets with a great degree of control over the composition and shape. Starting with hexagonal nanoplatelets of cubic Cu2−xSe, ternary CuAgSe nanoplatelets were generated through a rapid ion exchange reaction at 300 K using AgNO3 solution. The Cu2−xSe nanoplatelet template and the final CuAgSe nanoplatelets were analyzed by electron microscopy and X-ray diffraction (XRD). It was found that both the low temperature pseudotetragonal and the high temperature cubic forms of CuAgSe phase were created while maintaining the morphology of the Cu2−xSe nanoplatelet template. Thermal and electronic transport measurements of hot-pressed pellets of the synthesized CuAgSe nanoplatelets showed a drastic reduction in the thermal conductivity and a sharp transition from n-type (S = −45 μV K−1) to p-type (S = +200 μV K−1) semiconducting behavior upon heating above the structural transition from the low temperature orthorhombic to the high temperature super-ionic cubic phase. This simple reaction process utilizing a template nanostructure matrix represents an energy efficient, cost-efficient, and versatile strategy to create interesting materials with lower defect density and superior thermoelectric performance.

Graphical abstract: Rapid direct conversion of Cu2−xSe to CuAgSe nanoplatelets via ion exchange reactions at room temperature

Supplementary files

Article information

Article type
Communication
Submitted
05 Mar 2015
Accepted
01 May 2015
First published
05 May 2015

Nanoscale, 2015,7, 9452-9456

Author version available

Rapid direct conversion of Cu2−xSe to CuAgSe nanoplatelets via ion exchange reactions at room temperature

N. A. Moroz, A. Olvera, G. M. Willis and P. F. P. Poudeu, Nanoscale, 2015, 7, 9452 DOI: 10.1039/C5NR01451D

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