Solid-state synthesis of Si<sub>1−<i>x</i></sub>Ge<sub><i>x</i></sub> nanoalloys with composition-tunable energy gaps and visible to near infrared optical properties

Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> alloy nanocrystals (NCs) are a class of benign semiconductors that show size and composition-tunable energy gaps and promising optical properties because of the lattice disorder. The random distribution of elements within the alloys can lead to efficient light-matter interactions, making them attractive for Si-compatible optoelectronic devices, transistors, charge storage, and memory applications. However, the fabrication of discrete, quantum-confined alloys has proved a challenging task. Herein, we report solid-state co-disproportionation of a hydrogen silsesquioxane (HSQ)/GeI<sub>2</sub> composite precursor to produce homogeneous Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> NCs with control over the diameter (5.9 ± 0.7-7.8 ± 1.1 nm) and composition (<i>x</i> = 0-14.4%) with strong size confinement effects and visible to near IR absorption and emission properties. As-synthesized alloys show an expanded diamond cubic Si structure, a systematic red-shift of Si-Si Raman peak, and emergence of Si-Ge/Ge-Ge peaks with increasing Ge, consistent with the admixture of isovalent elements. Surface analysis of alloys reveals Si<sup>0</sup>/Ge<sup>0</sup> core and Si<sup><i>n</i>+</sup>/Ge<sup><i>n</i>+</sup> surface species and efficient surface functionalization with alkyl ligands <i>via</i> thermal hydrosilylation and/or hydrogermylation. Alloy NCs exhibit absorption onsets (2.26-1.92 eV), indirect (1.53-1.80 eV) and direct (2.88-2.47 eV) energy gaps, and photoluminescence (PL) maxima (1.40-1.27 eV) that can be tuned by manipulating the diameter and/or composition. The experimental PL energies are consistent with those predicted by density functional theory (DFT), suggesting that the PL originates from NC core electronic transitions. The facile low-temperature solid-state synthesis and control over physical properties realized in this study will allow discrete Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> NCs to emerge as low to nontoxic, earth-abundant, and Si-compatible nanostructures for a broad range of electronic and photonic technologies.

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Publication Details

Journal
Nanoscale
Published
2024-12-04
DOI
https://doi.org/10.1039/d4nr03472d
Citations
1
Primary Topic
Silicon Nanostructures and Photoluminescence
Type
article
Field-Weighted Citation Impact
0.12

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Solid-state synthesis of Si1−xGex nanoalloys with composition-tunable energy gaps and visible to near infrared optical properties

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article

Solid-state synthesis of Si1−xGex nanoalloys with composition-tunable energy gaps and visible to near infrared optical properties

D. Pate, Indika U. Arachchige, Ü. Özgür, Ka Un Lao, Lisa S. Graves, Corentin Villot, Griffin C. Spence, Roshana M Fouzie
article en
1 citations

Abstract

Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> alloy nanocrystals (NCs) are a class of benign semiconductors that show size and composition-tunable energy gaps and promising optical properties because of the lattice disorder. The random distribution of elements within the alloys can lead to efficient light-matter interactions, making them attractive for Si-compatible optoelectronic devices, transistors, charge storage, and memory applications. However, the fabrication of discrete, quantum-confined alloys has proved a challenging task. Herein, we report solid-state co-disproportionation of a hydrogen silsesquioxane (HSQ)/GeI<sub>2</sub> composite precursor to produce homogeneous Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> NCs with control over the diameter (5.9 ± 0.7-7.8 ± 1.1 nm) and composition (<i>x</i> = 0-14.4%) with strong size confinement effects and visible to near IR absorption and emission properties. As-synthesized alloys show an expanded diamond cubic Si structure, a systematic red-shift of Si-Si Raman peak, and emergence of Si-Ge/Ge-Ge peaks with increasing Ge, consistent with the admixture of isovalent elements. Surface analysis of alloys reveals Si<sup>0</sup>/Ge<sup>0</sup> core and Si<sup><i>n</i>+</sup>/Ge<sup><i>n</i>+</sup> surface species and efficient surface functionalization with alkyl ligands <i>via</i> thermal hydrosilylation and/or hydrogermylation. Alloy NCs exhibit absorption onsets (2.26-1.92 eV), indirect (1.53-1.80 eV) and direct (2.88-2.47 eV) energy gaps, and photoluminescence (PL) maxima (1.40-1.27 eV) that can be tuned by manipulating the diameter and/or composition. The experimental PL energies are consistent with those predicted by density functional theory (DFT), suggesting that the PL originates from NC core electronic transitions. The facile low-temperature solid-state synthesis and control over physical properties realized in this study will allow discrete Si<sub>1-<i>x</i></sub>Ge<sub><i>x</i></sub> NCs to emerge as low to nontoxic, earth-abundant, and Si-compatible nanostructures for a broad range of electronic and photonic technologies.

NanoscaleVol. 17(6)
Virginia Commonwealth University (US)
National Science Foundation, Virginia Commonwealth University, Division of Materials Research
Openalex Percentile: Top 57%
Silicon Nanostructures and Photoluminescence
0.12
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