Charge-governed phase manipulation of few-layer tellurium. Issue 47 (22nd November 2018)
- Record Type:
- Journal Article
- Title:
- Charge-governed phase manipulation of few-layer tellurium. Issue 47 (22nd November 2018)
- Main Title:
- Charge-governed phase manipulation of few-layer tellurium
- Authors:
- Wang, Cong
Zhou, Xieyu
Qiao, Jingsi
Zhou, Linwei
Kong, Xianghua
Pan, Yuhao
Cheng, Zhihai
Chai, Yang
Ji, Wei - Abstract:
- Abstract : Te few-layer allotropes could be selectively stabilized and be reversibly transformed using charge doping. Among them, a novel chiral metallic phase emerges in a Te trilayer under electron doping. Abstract : Few-layer tellurium is an emerging quasi-one-dimensional layered material. The striking feature of Te is its presence as various few-layer allotropes (α–δ). Although these allotropes offer substantially different physical properties, only the α phase has been synthesized in neutral few-layers as it is so far the most stable few-layer form. Herein, we show that hole or electron doping could maintain a certain Te phase. The β, α, γ and δ phases appear as the most stable forms of Te bilayer, in sequence, with bandgap variations over 1 eV. In Te trilayer, a novel metallic chiral α + δ phase emerges, leading to the appearance of chirality. Transitions among these phases, understood at the wavefunction level, are accompanied by the emergence or elimination of inversion centers (α–β, α–γ, α–α + δ), structural anisotropy (α–γ, γ–δ) and chirality (α–α + δ), which could result in substantial changes in optical and other properties. In light of these findings, our work opens a new avenue for stabilizing different allotropes of layered materials; this is crucial for using their outstanding properties. This study also suggests the possibility of building mono-elemental electronic and optoelectronic heterostructures or devices, which are attractive for future applicationsAbstract : Te few-layer allotropes could be selectively stabilized and be reversibly transformed using charge doping. Among them, a novel chiral metallic phase emerges in a Te trilayer under electron doping. Abstract : Few-layer tellurium is an emerging quasi-one-dimensional layered material. The striking feature of Te is its presence as various few-layer allotropes (α–δ). Although these allotropes offer substantially different physical properties, only the α phase has been synthesized in neutral few-layers as it is so far the most stable few-layer form. Herein, we show that hole or electron doping could maintain a certain Te phase. The β, α, γ and δ phases appear as the most stable forms of Te bilayer, in sequence, with bandgap variations over 1 eV. In Te trilayer, a novel metallic chiral α + δ phase emerges, leading to the appearance of chirality. Transitions among these phases, understood at the wavefunction level, are accompanied by the emergence or elimination of inversion centers (α–β, α–γ, α–α + δ), structural anisotropy (α–γ, γ–δ) and chirality (α–α + δ), which could result in substantial changes in optical and other properties. In light of these findings, our work opens a new avenue for stabilizing different allotropes of layered materials; this is crucial for using their outstanding properties. This study also suggests the possibility of building mono-elemental electronic and optoelectronic heterostructures or devices, which are attractive for future applications in electronics. … (more)
- Is Part Of:
- Nanoscale. Volume 10:Issue 47(2018)
- Journal:
- Nanoscale
- Issue:
- Volume 10:Issue 47(2018)
- Issue Display:
- Volume 10, Issue 47 (2018)
- Year:
- 2018
- Volume:
- 10
- Issue:
- 47
- Issue Sort Value:
- 2018-0010-0047-0000
- Page Start:
- 22263
- Page End:
- 22269
- Publication Date:
- 2018-11-22
- Subjects:
- Nanoscience -- Periodicals
Nanotechnology -- Periodicals
620.505 - Journal URLs:
- http://www.rsc.org/Publishing/Journals/NR/Index.asp ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c8nr07501h ↗
- Languages:
- English
- ISSNs:
- 2040-3364
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9830.266000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9044.xml