Quantum size effects on the optical properties of nc-Si QDs embedded in an a-SiOx matrix synthesized by spontaneous plasma processing
文献情報
Debajyoti Das, Arup Samanta
Quantum confinement effects on optical transitions in ensembles of nc-Si QDs in an a-SiOx matrix has become evident by simultaneously considering the dielectric function dispersions obtained by optical modeling with spectroscopic ellipsometry, the absorption edge, and the photoluminescence peak. Diminution of the peak amplitude in the ε2-spectra for reducing the diameter of nc-Si QDs could arise due to the disappearance of excitonic effects in the E1 transition, while the peak broadening indicates an amplification of disorder in Si QDs. An energy blue shift happens to take place in an analogous fashion for all the characteristic parameters, upon decreasing the size of the nc-Si QDs for diameters in the range 6.5 < d < 2.0 nm. The band gap widening with the reduction of QD size is well supported by the first-principles calculations based on quantum confinement, while studies on the Stokes shift in the optical gap from the PL data could provide an understanding of the imperfect passivation of the surface defects on tiny nc-Si QDs. Low dimensional nc-Si QDs (∼2 nm in diameter) assembled in a large density (∼2.3 × 1012 cm−2) embedded in an a-SiOx matrix synthesized by spontaneous and low-temperature (300 °C) RF plasma processing, compatible to CMOS technology, are highly conducive for device applications. Systematic changes in composition and characteristics, including the thickness, of the individual sub-layers of the nc-Si QD thin films can be comprehensively pursued through a nondestructive process by ellipsometric simulation which could, thereby, enormously contribute to the precise optimization of the deposition parameters suitable for specific device fabrication e.g., all-silicon tandem solar cells and light emitting diodes, using silicon nanotechnology.
関連文献
Peroxy mediated Csp2–Csp3 dehydrogenative coupling: regioselective functionalization of coumarins and coumarin-3-carboxylic acids
Farnaz Jafarpour, Masoumeh Darvishmolla
DOI: 10.1039/C7OB02771K
Formation of β-cyano-ketones through cyanide-promoted ring-opening of cyclic organic carbonates
Jixiang Ni, Àlex Cristòfol
DOI: 10.1039/D1QO00770J
Metal-free oxidative cyclization of trifluoroacetimidohydrazides with methylhetarenes: a facile access to 3-hetaryl-5-trifluoromethyl-1,2,4-triazoles
Jiajun Zhang, Tian-Hui Xu, Zhengkai Chen
DOI: 10.1039/D1QO00790D
The synthesis of mono-alkyl phosphates and their derivatives: an overview of their nature, preparation and use, including synthesis under plausible prebiotic conditions
DOI: 10.1039/C8OB00469B
Facile access to 2-acyloxy-, aryloxy- and alkenyloxy-2H-azirines via an SN2′–SN2′ cascade in 2-halo-2H-azirines
Nikolai V. Rostovskii, Ilia A. Smetanin, Anastasiya V. Agafonova, Pavel A. Sakharov, Julia O. Ruvinskaya, Alexander F. Khlebnikov, Mikhail S. Novikov
DOI: 10.1039/C8OB00553B
Chemoselective hydroborative reduction of nitro motifs using a transition-metal-free catalyst
Yinpeng Lou, Haijian Wu, Xinxin Qi, Aiguo Zhong
DOI: 10.1039/D1QO00705J
Recent advances in multi-component reactions and their mechanistic insights: a triennium review
Stephy Elza John, Shivani Gulati, Nagula Shankaraiah
DOI: 10.1039/D0QO01480J
Anti-HIV activity of new higher order G-quadruplex aptamers obtained from tetra-end-linked oligonucleotides
F. Nici, G. Oliviero, A. P. Falanga, S. D'Errico, M. Marzano, D. Musumeci, D. Montesarchio, S. Noppen, C. Pannecouque, G. Piccialli, N. Borbone
DOI: 10.1039/C7OB02346D
Hybrid phosphorus–viologen dendrimers as new soft nanoparticles: design and properties
Maria Zablocka, Karol Ciepluch, Katarzyna Milowska, Maria Bryszewska, Dzmitry Shcharbin, Nadia Katir, Abdelkrim El Kadib
DOI: 10.1039/D1QO00511A
こちらもおすすめ
2-メトキシ-4-(メチルスルフィニル)アミンの主な用途は何ですか?
2-メトキシ-4-(メチルスルフィニル)アミンは、主に医薬品および農薬の製造に使用されます。また、合成化学の一部として研究用材料としても利用されます。
4,6-二氯-N-甲基ピラミジンアミンの代替品はありますか?
代替品としては、4,6-二クロロピラミジンアミンや他のピラミジン系化合物が考えられます。ただし、目的と用途によって最適な代替品は異なります。
6-氯-4-甲基-1H-吲哚を含む廃棄物はどのように処理すべきですか?
6-氯-4-甲基-1H-吲哚の廃棄物は、適切な容器に収集し、密閉して保管します。温度は常温、湿度は低く、直射日光を避けて保管することを推奨します。廃棄処理は専門...
2-フローユロ-4-(トリフルオロメチル)ベンゾイドについて「に適用される法規ガイドラインは何ですか」
2-フローユロ-4-(トリフルオロメチル)ベンゾイドのCAS番号は207974-08-1です。この化合物はGHS分類で毒性物質と有害な反応物質として分類されます...
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸はどのように保存すればよいですか?
4-ニトロフェニルN-[(ベンゼルオキシルカーボンイル]グリシングリシングリシン酸は、室温で暗所に保管し、乾燥した環境で保存することを推奨します。容器は密閉性の...
イソデスロラタドリンの代替品はありますか?
イソデスロラタドリンの代替品としては、デスロラタドリンや他の抗ヒスタミン薬が挙げられます。具体的には、デスロラタドリン、ラセカミド、フェルタドリンなどが、症状や...
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐はどのように合成されますか?
5-甲氧基-1,2,3,4-四氢异喹啉盐酸盐の一般的な合成方法は、メタノール中で5-メトキシ-1,2,3,4-四ヒュドロイソキシンを塩酸で塩化します。この反応で...
4-アミノ-5-メトキシ-2-トルエンサルホニック酸についての法規ガイドラインは何ですか?
CAS番号6471-78-9の4-アミノ-5-メトキシ-2-トルエンサルホニック酸は、GHS分類では corrosive(腐食性)と識別されます。EUのREAC...
甲基孕酮を取り扱う際の実験室安全事項は何ですか?
甲基孕酮の取り扱いは、PPE(個人保護具)の使用が必要な重要な安全事項を伴います。防塵マスク、ゴーグル、手袋を着用することが推奨されます。ドラフトチャンバーを使...
掲載誌
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











![1-Naphthalenesulfonic acid, 2-[(2-hydroxy-1-naphthalenyl)azo]-, bariumsalt (2:1) structure 1-Naphthalenesulfonic acid, 2-[(2-hydroxy-1-naphthalenyl)azo]-, bariumsalt (2:1) structure](https://static.chemtradehub.com/structs/110/1103-38-4-0b33.webp)


![5-Acetyl-2,3-dihydrobenzo[b]furan structure 5-Acetyl-2,3-dihydrobenzo[b]furan structure](https://static.chemtradehub.com/structs/908/90843-31-5-eea4.webp)