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Symmetry-defying iron pyrite (FeS?) nanocrystals through oriented attachment.

ABSTRACT: Iron pyrite (fool's gold, FeS?) is a promising earth abundant and environmentally benign semiconductor material that shows promise as a strong and broad absorber for photovoltaics and high energy density cathode material for batteries. However, controlling FeS? nanocrystal formation (composition, size, shape, stoichiometry, etc.) and defect mitigation still remains a challenge. These problems represent significant limitations in the ability to control electrical, optical and electrochemical properties to exploit pyrite's full potential for sustainable energy applications. Here, we report a symmetry-defying oriented attachment FeS? nanocrystal growth by examining the nanostructure evolution and recrystallization to uncover how the shape, size and defects of FeS? nanocrystals changes during growth. It is demonstrated that a well-controlled reaction temperature and annealing time results in polycrystal-to-monocrystal formation and defect annihilation, which correlates with the performance of photoresponse devices. This knowledge opens up a new tactic to address pyrite's known defect problems.

SUBMITTER: Gong M

PROVIDER: S-EPMC3697776 | biostudies-literature | 2013

REPOSITORIES: biostudies-literature

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Symmetry-defying iron pyrite (FeS₂) nanocrystals through oriented attachment.

Gong Maogang M Kirkeminde Alec A Ren Shenqiang S

Scientific reports 20130101

Iron pyrite (fool's gold, FeS₂) is a promising earth abundant and environmentally benign semiconductor material that shows promise as a strong and broad absorber for photovoltaics and high energy density cathode material for batteries. However, controlling FeS₂ nanocrystal formation (composition, size, shape, stoichiometry, etc.) and defect mitigation still remains a challenge. These problems represent significant limitations in the ability to control electrical, optical and electrochemical prop ...[more]

PMID: 23807691

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Project description:Augmenting the oriented attachment (OA) crystal growth phenomena, herein, we demonstrate fabrication of ultrathin CuO nanowires from self-assembled one-dimensional (1D) nanowires of Cu(OH)2 nanocrystals. A facile environmentally benign sol-gel approach, which utilizes base-catalyzed hydrolysis followed by directed self-assembly and crystal growth of nanocrystals, is developed to prepare Cu(OH)2 nanowires. The sol of Cu(OH)2 nanocrystals shows aggregative self-assembly guided by the OA crystal growth process to form ultrathin Cu(OH)2 nanowires, with an average length of 675 ± 4 nm and diameter of 6 ± 2 nm. The time-dependent UV-visible spectral traces, along with real-time imaging of nanocrystals self-assembly and growth under the transmission electron microscope, are evidenced the concept of the OA crystal growth directed self-assembly, yielding 1D colloidal nanoarrays of Cu(OH)2. The powder XRD traces collected during the self-assembly and crystal growth process reveal the directional aggregative crystal growth along the facet of [001], confirming the OA directed crystal growth and fusion of nanocrystals to yield 1D nanostructures. The gradual blue-shift in optical absorption maxima from 770 nm in initial precursor solution, to 670 nm for Cu(OH)2 nanocrystals sol, and finally to 647 nm for self-assembled 1D Cu(OH)2 nanowires have further evidenced the formation of Cu(OH)2 nanowires. Upon subjecting self-assembled Cu(OH)2 nanowires for post-annealing treatment, ultrathin CuO nanowires with average length of 7 ± 0.50 μm and diameter of 27 ± 2 nm is obtained in high purity. The experimental powder XRD patterns of Cu(OH)2 and CuO nanowires match the simulated XRD patterns, indexing the crystal unit cell structures to orthorhombic and monoclinic, respectively. The tailored narrow optical band gaps for Cu(OH)2 and CuO nanowires are found to be 1.51 eV and 1.10 eV. The theoretical band gap predicted for Cu(OH)2 nanowires is 1.52 eV and is in good agreement with its optical band gap, whereas theoretical band computed for CuO nanowires is 0.13 eV lower than from its optical band gap.

Dataset Information

Symmetry-defying iron pyrite (FeS?) nanocrystals through oriented attachment.

Publications

Symmetry-defying iron pyrite (FeS₂) nanocrystals through oriented attachment.

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