A cyclopentasilane–borane compound as a liquid precursor for p-type semiconducting Si. Issue 16 (19th April 2021)
- Record Type:
- Journal Article
- Title:
- A cyclopentasilane–borane compound as a liquid precursor for p-type semiconducting Si. Issue 16 (19th April 2021)
- Main Title:
- A cyclopentasilane–borane compound as a liquid precursor for p-type semiconducting Si
- Authors:
- Masuda, Takashi
Nakayama, Maui
Saito, Kimihiko
Katayama, Hirotaka
Terakawa, Akira - Abstract:
- Abstract : A liquid precursor for p-type semiconducting Si is synthesized using the dehydrogenative condensation reaction between cyclopentasilane and boron hydride. Abstract : Although little is known about the reaction mechanism between cyclopentasilane (CPS: cyclic Si5 H10 ) and borane (BH3 ), the reaction product is known to be a liquid precursor for p-type semiconducting Si. Therefore, investigation of the reaction mechanism enables more functional material design and contributes to the realization of printable Si semiconductors. Here, we investigated the interaction between CPS and BH3 using density functional theory (DFT) calculations. The calculations showed the occurrence of a dehydrogenative condensation reaction with an energy barrier less than 10 kcal mol −1 . CPS and BH3 act as Lewis bases and acids, respectively, and form somewhat stable reactant complexes with monobridged hydrogen bonds through electrostatic interactions between the positively charged Si atoms and negatively charged B atoms. The monobridged hydrogen bonds initiate dehydrogenation because they abstract other hydrogen atoms in the compound. Eventually, liquid-phase hydrosilanes with Si–B bonds remain as the reaction product. This reaction model and reaction products were also evaluated experimentally using nuclear magnetic resonance spectroscopy, gas chromatography, and gel permeation chromatography. Characterization of the printed Si film also showed that the reaction product can be used as anAbstract : A liquid precursor for p-type semiconducting Si is synthesized using the dehydrogenative condensation reaction between cyclopentasilane and boron hydride. Abstract : Although little is known about the reaction mechanism between cyclopentasilane (CPS: cyclic Si5 H10 ) and borane (BH3 ), the reaction product is known to be a liquid precursor for p-type semiconducting Si. Therefore, investigation of the reaction mechanism enables more functional material design and contributes to the realization of printable Si semiconductors. Here, we investigated the interaction between CPS and BH3 using density functional theory (DFT) calculations. The calculations showed the occurrence of a dehydrogenative condensation reaction with an energy barrier less than 10 kcal mol −1 . CPS and BH3 act as Lewis bases and acids, respectively, and form somewhat stable reactant complexes with monobridged hydrogen bonds through electrostatic interactions between the positively charged Si atoms and negatively charged B atoms. The monobridged hydrogen bonds initiate dehydrogenation because they abstract other hydrogen atoms in the compound. Eventually, liquid-phase hydrosilanes with Si–B bonds remain as the reaction product. This reaction model and reaction products were also evaluated experimentally using nuclear magnetic resonance spectroscopy, gas chromatography, and gel permeation chromatography. Characterization of the printed Si film also showed that the reaction product can be used as an effective liquid precursor for p-type semiconducting Si. … (more)
- Is Part Of:
- Journal of materials chemistry. Volume 9:Issue 16(2021)
- Journal:
- Journal of materials chemistry
- Issue:
- Volume 9:Issue 16(2021)
- Issue Display:
- Volume 9, Issue 16 (2021)
- Year:
- 2021
- Volume:
- 9
- Issue:
- 16
- Issue Sort Value:
- 2021-0009-0016-0000
- Page Start:
- 5387
- Page End:
- 5395
- Publication Date:
- 2021-04-19
- Subjects:
- Materials -- Periodicals
Chemistry, Analytic -- Periodicals
Optical materials -- Research -- Periodicals
Electronics -- Materials -- Research -- Periodicals
543.0284 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/tc# ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1tc00165e ↗
- Languages:
- English
- ISSNs:
- 2050-7526
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5012.205300
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 16718.xml