A nanostructured SnTe phase was produced by mechanical alloying after 2 h of milling. Part of the as-milled powder was annealed and its X-ray diffraction (XRD) pattern was recorded. The XRD patterns of the as-milled and annealed samples were refined using the Rietveld method. After annealing, partial decomposition of the SnTe phase was observed and corroborated by estimating the mean crystallite size using a Willianson-Hall plot. The Cowley-Warren parameter α SnTe CWfor the first coordination shell was calculated, showing a preference for homopolar pairs. This preference is consistent with the partial decomposition observed. According to the optical absorbance spectra, the band gap energy is inversely proportional to crystallite size, following a decaying exponential function. From the photoacoustic absorption spectroscopy measurements, the thermal diffusivity parameter and the transport properties of as-milled and annealed SnTe powder were determined.

A nanostructured Cr11Ge19 phase was produced by mechanical alloying for 15 h. Decomposition occurred for larger milling times, yielding Cr, Ge, Cr2O3 and GeO2. According to the Cr-Ge phase diagram, the Cr11Ge19 phase is stable up to ≈ 928 oC, but, when submitted to milling, a structural instability causes its decomposition. We studied this structural instability using the coordination numbers and interatomic distances of bulk Cr11Ge19 to simulate the structure factors SCrCr(K), SCrGe(K), and SGeGe(K). The radial distribution functions RDFCrCr(R), RDFCrGe(R) and RDFGeGe(R) were obtained by Fourier transforming the Sij(K) factors, and an important chemical disorder up to ≈7 Å was observed in the RDFCrGe(R) and RDFGeGe(R) functions. This chemical disorder was quantified using Cowley-Warren α ij CW parameter. The thermoelectric properties of the Cr11Ge19 phase were also studied.