Abstract

Bi-Pb-chalcogenides of the aleksite series represent homologous mixed-layer compounds derived from tetradymite (Bi2Te2S). Considering tetradymite as composed of five-atom (Bi2Te2S) layers, the named minerals of the aleksite homologous series, aleksite (PbBi2Te2S2) and saddlebackite, (Pb2Bi2Te2S3) have been considered as phases formed by regular stacking of longer seven- and nine-atom layers. High-angle annular dark-field scanning transmission electron microscope (HAADF-STEM) imaging of thinned foils prepared in-situ on domains deemed homogeneous from electron probe microanalysis, STEM energy-dispersive X-ray spectrometry (EDS) element mapping and fast Fourier transforms (FFTs) from the images offer new insights into these structures. The hitherto-unnamed phase, PbBi4Te4S3, previously interpreted as regular intergrowths of five- and seven-atom layers, is characterized in terms of regular repeats of five- and seven-atom layers over distances of at least 350 nm, defining the (57), or 24H polytype. Imaging of other domains in the same lamella with identical composition at the electron microprobe scale reveals the presence of two additional polytypes: (5559), or 48H; and (557.559) or 72H. Unit cell dimensions for all three polytypes of PbBi4Te4S3 can be both measured and predicted from the HAADF STEM imaging and FFTs. STEM EDS mapping of each polytype confirm the internal structure of each layer. Lead and S occur within the centre of the layers, i.e., Te–Bi–S–Pb–S–Bi–Te in the seven-atom layer, Te–Bi–S–Pb–S–Pb–S–Bi–Te in the nine-atom layer, and so on. Polytypism is an intrinsic feature of the aleksite series, with each named mineral or unnamed phase, except the simple five-atom layer, defined by several alternative stacking sequences of different length, readily explaining the differing c values given in previous work. Homology is defined in terms of layer width and the stacking arrangement of those layers. Coherent structures of the same composition need not only be built of layers of adjacent size (i.e., five- and seven-atom layers) but, as exemplified by the (5559) polytype, may also contain non-adjacent layers, a finding not anticipated in previous work. New polysomes remain to be discovered in nature and each potentially exists as multiple polytypes. The present study further emphasizes the utility of HAADF STEM imaging and atomic-scale STEM EDS element mapping as an optimal tool for tracking stacking sequences and characterising structures in mixed-layer compounds.

Highlights

  • Bismuth-lead-chalcogenides of the informally named aleksite series, Pbn Bi4 Te4 Sn+2 [1] represent a modular series derived from tetradymite, Bi2 Te2 S, where n = 0

  • They represent a discrete group of named minerals and as-yet unnamed phases, whose structures are derived from the tetradymite group of bismuth chalcogenides [2,3]

  • The (57) polytype of PbBi4Te4S3 is characterized by electron diffraction/fast Fourier transforms (FFTs) patterns as being directly comparable with analogous (57)phases from the tetradymite group, e.g., tsumoite, BiTe [3], whereby displacement shifts introduced by a modulation vector underpin the stacking sequence and, implicitly, their composition

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Summary

Introduction

Bismuth-lead-chalcogenides of the informally named aleksite series, Pbn Bi4 Te4 Sn+2 [1] represent a modular series derived from tetradymite, Bi2 Te2 S, where n = 0 These phases are reported as minor constituents of several gold-bearing ore deposits [1]. Cook et al [1] provided new paragenetic and microanalytical data for aleksite series minerals in samples from three additional localities: the Clogau mine, Wales, U.K.; the Iilijärvi deposit, Southwest Finland; and from Fragant, Austria. These data indicated the possible existence of several additional, as-yet unnamed phases. These unnamed phases have compositions between that of tetradymite and aleksite, between aleksite and saddlebackite, and in the range Pb5 Bi4 Te4 S7 to

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