Thermally-Induced Dehydrogenative Coupling of Organosilanes and H-Terminated Silicon Quantum Dots onto Germanane Surfaces

Author(s):  
Haoyang Yu ◽  
Alyxandra Thiessen ◽  
Md Asjad Hossain ◽  
Marc Julian Kloberg ◽  
Bernhard Rieger ◽  
...  

<div><div><div><p>Covalently bonded organic monolayers play important roles in defining the solution processability, ambient stability, and electronic properties of two-dimensional (2D) materials such as Ge nanosheets (GeNSs); they also hold promise of providing avenues for the fabrication of future generation electronic and optical devices. Functionalization of GeNS normally involves surface moieties linked through covalent Ge−C bonds. In the present contribution we extend the scope of surface linkages to include Si−Ge bonding and present the first demonstration of heteronuclear dehydrocoupling of organosilanes to hydride-terminated GeNSs obtained from the deintercalation and exfoliation of CaGe2. We further exploit this new surface reactivity and demonstrated the preparation of directly bonded silicon quantum dot-Ge nanosheet hybrids.</p></div></div></div>

2020 ◽  
Author(s):  
Haoyang Yu ◽  
Alyxandra Thiessen ◽  
Md Asjad Hossain ◽  
Marc Julian Kloberg ◽  
Bernhard Rieger ◽  
...  

<div><div><div><p>Covalently bonded organic monolayers play important roles in defining the solution processability, ambient stability, and electronic properties of two-dimensional (2D) materials such as Ge nanosheets (GeNSs); they also hold promise of providing avenues for the fabrication of future generation electronic and optical devices. Functionalization of GeNS normally involves surface moieties linked through covalent Ge−C bonds. In the present contribution we extend the scope of surface linkages to include Si−Ge bonding and present the first demonstration of heteronuclear dehydrocoupling of organosilanes to hydride-terminated GeNSs obtained from the deintercalation and exfoliation of CaGe2. We further exploit this new surface reactivity and demonstrated the preparation of directly bonded silicon quantum dot-Ge nanosheet hybrids.</p></div></div></div>


Micromachines ◽  
2022 ◽  
Vol 13 (1) ◽  
pp. 92
Author(s):  
Hongyan Yang ◽  
Yunzheng Wang ◽  
Zian Cheak Tiu ◽  
Sin Jin Tan ◽  
Libo Yuan ◽  
...  

In the advancement of photonics technologies, all-optical systems are highly demanded in ultrafast photonics, signal processing, optical sensing and optical communication systems. All-optical devices are the core elements to realize the next generation of photonics integration system and optical interconnection. Thus, the exploration of new optoelectronics materials that exhibit different optical properties is a highlighted research direction. The emerging two-dimensional (2D) materials such as graphene, black phosphorus (BP), transition metal dichalcogenides (TMDs) and MXene have proved great potential in the evolution of photonics technologies. The optical properties of 2D materials comprising the energy bandgap, third-order nonlinearity, nonlinear absorption and thermo-optics coefficient can be tailored for different optical applications. Over the past decade, the explorations of 2D materials in photonics applications have extended to all-optical modulators, all-optical switches, an all-optical wavelength converter, covering the visible, near-infrared and Terahertz wavelength range. Herein, we review different types of 2D materials, their fabrication processes and optical properties. In addition, we also summarize the recent advances of all-optical modulation based on 2D materials. Finally, we conclude on the perspectives on and challenges of the future development of the 2D material-based all-optical devices.


2020 ◽  
Vol 22 (39) ◽  
pp. 22140-22156
Author(s):  
Xin-Ping Zhai ◽  
Bo Ma ◽  
Qiang Wang ◽  
Hao-Li Zhang

Two-dimensional materials are now excelling in yet another arena of ultrafast photonics, including optical modulation through optical limiting/mode-locking, photodetectors, optical communications, integrated miniaturized all-optical devices, etc.


2019 ◽  
Vol 7 (11) ◽  
pp. 3360-3368 ◽  
Author(s):  
Xiaodong Zhou ◽  
Fei Li ◽  
Yanxia Xing ◽  
Wanxiang Feng

The magneto-optical effects play a prominent role in probing the exotic magnetism in 2D materials. Here, we present that the magneto-optical Kerr and Faraday effects in carrier-doped nitrogen–graphene crystals can be effectively mediated by electric, magnetic, and strain fields. Our results indicate that nitrogen–graphene crystals provide a novel 2D material platform for nano-spintronics and magneto-optical devices.


2020 ◽  
Author(s):  
Haoyang Yu ◽  
Chuyi Ni ◽  
Alyxandra Thiessen ◽  
Ziqi Li ◽  
Jonathan G.C. Veinot

<div> <div> <div> <p>Polygermanes are germanium-based analogues of polyolefins and possess polymer backbones made up catenated Ge atoms. In the present contribution we report the preparation of a stable germanium polyethylene analogue – polydihydrogermane (i.e., (GeH2)n) – via two straightforward approaches that involve topotactic deintercalation of the CaGe Zintl phase. The resulting (GeH2)n possess morphologically dependent chemical and electronic properties and thermally decompose to yield amorphous hydrogenated Ge. We also show that the resulting (GeH2)n provide a platform from which functionalized polygermanes can be prepared via thermally-induced hydrogermylation-mediated pendant group substitution. This facile one-step derivatization reaction exploits Ge–H reactivity and opens the door to a wide array of tailored functional polygermanes. </p> </div> </div> </div>


1986 ◽  
Vol 90 (14) ◽  
pp. 3054-3056 ◽  
Author(s):  
Sidney R. Cohen ◽  
Ron Naaman ◽  
Jacob Sagiv

2017 ◽  
Vol 5 (19) ◽  
pp. 1700257 ◽  
Author(s):  
Sathish C. Dhanabalan ◽  
Balaji Dhanabalan ◽  
Joice S. Ponraj ◽  
Qiaoliang Bao ◽  
Han Zhang

2003 ◽  
Vol 762 ◽  
Author(s):  
Andrea Lehner ◽  
Georg Steinhoff ◽  
Martin S. Brandt ◽  
Martin Eickhoff

AbstractUsing thermally induced hydrosilylation, organic molecules were covalently bonded to H-terminated crystalline silicon (111) and hydrogenated amorphous silicon (a-Si:H) surfaces. The resulting chemical surface structure was analyzed by X-ray photoelectron spectroscopy (XPS) and compared to that of silicon surfaces covered by a native oxide or terminated with hydrogen. For both kinds of substrates, the presence of oxygen on the surface is found to hinder the hydrosilylation reaction. Stable H-termination as a starting point for a successful hydrosilylation can be obtained on a-Si:H surfaces with much less technological effort than on crystalline silicon surfaces. Photoconductivity measurements of the different a-Si:H surfaces at low intensity of illumination (monomolecular recombination regime) indicate that the hydrosilylated surface has less defects than the H-terminated surfaces or surfaces covered with native oxide. Spin-dependent photoconductivity measurements identify the dominant paramagnetic defect at the hydrosilylated a-Si:H surface to be the silicon dangling bond.


Nano Letters ◽  
2001 ◽  
Vol 1 (9) ◽  
pp. 491-494 ◽  
Author(s):  
Srikanth Ranganathan ◽  
Ilson Steidel ◽  
Franklin Anariba ◽  
Richard L. McCreery

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