Alkali ion doping of silicon

1964 ◽  
Vol 52 (3) ◽  
pp. 301-302 ◽  
Author(s):  
J.O. McCaldin ◽  
A.E. Widmer
Keyword(s):  
CrystEngComm ◽  
2015 ◽  
Vol 17 (9) ◽  
pp. 1997-2003 ◽  
Author(s):  
Dominika Wawrzynczyk ◽  
Marek Samoć ◽  
Marcin Nyk

2016 ◽  
Vol 138 (28) ◽  
pp. 8875-8882 ◽  
Author(s):  
Tian-Ran Wei ◽  
Gangjian Tan ◽  
Xiaomi Zhang ◽  
Chao-Feng Wu ◽  
Jing-Feng Li ◽  
...  

2010 ◽  
Vol 195 (10) ◽  
pp. 3316-3322 ◽  
Author(s):  
A. Aboulaich ◽  
D.E. Conte ◽  
J. Olivier-Fourcade ◽  
C. Jordy ◽  
P. Willmann ◽  
...  

2020 ◽  
Vol 5 (3) ◽  
pp. 236-251
Author(s):  
Eshwara I. Naik ◽  
Halehatty S.B. Naik ◽  
Ranganaik Viswanath

Background: Various interesting consequences are reported on structural, optical, and photoluminescence properties of Zn1-xSmxO (x=0, 0.01, 0.03 and 0.05) nanoparticles synthesized by sol-gel auto-combustion route. Objective: This study aimed to examine the effects of Sm3+-doping on structural and photoluminescence properties of ZnO nanoparticles. Methods: Zn1-xSmxO (x=0, 0.01, 0.03 and 0.05) nanoparticles were synthesized by sol-gel auto combustion method. Results: XRD patterns confirmed the Sm3+ ion substitution through the undisturbed wurtzite structure of ZnO. The crystallite size was decreased from 24.33 to 18.46 nm with Sm3+ doping. The hexagonal and spherical morphology of nanoparticles was confirmed by TEM analysis. UV-visible studies showed that Sm3+ ion doping improved the visible light absorption capacity of Sm3+ iondoped ZnO nanoparticles. PL spectra of Sm3+ ion-doped ZnO nanoparticles showed an orange-red emission peak corresponding to 4G5/2→6HJ (J=7/2, 9/2 and 11/2) transition of Sm3+ ion. Sm3+ ion-induced PL was proposed with a substantial increase in PL intensity with a blue shift in peak upon Sm3+ content increase. Conclusion: Absorption peaks associated with doped ZnO nanoparticles were moved to a longer wavelength side compared to ZnO, with bandgap declines when Sm3+ ions concentration was increased. PL studies concluded that ZnO emission properties could be tuned in the red region along with the existence of blue peaks upon Sm3+ ion doping, which also results in enhancing the PL intensity. These latest properties related to Sm3+ ion-doped nanoparticles prepared by a cost-efficient process appear to be interesting in the field of optoelectronic applications, which makes them a prominent candidate in the form of red light-emitting diodes.


1990 ◽  
Vol 55 (5) ◽  
pp. 1149-1161
Author(s):  
Jiří Závada ◽  
Václav Pechanec ◽  
Oldřich Kocián

A powerful anion effect destabilizing alkali ion-crown complex formation has been found to operate in moderately concentrated protic (H2O, CH3OH, C2H5OH) solution, following the order HO- > AcO- > Cl- > Br- > NO3- > I- > NCS-. Evidence is provided that the observed effect does not originate from ion-pairing. A simple explanation is provided in terms of concordant hydrogen bond bridges of exalted stability between the gegenions, M+···OR-H···(OR-H)n···OR-H···A-. It is proposed that encapsulation of alkali ion by the macrocyclic ligand leads to a dissipation of the cation charge density destroying its ability to participate in the hydrogen bond bridge. An opposition against the alkali ion-crown complex formation arises accordingly in the solution in dependence on strength of the hydrogen bridge; for a given cation, the hydrogen bond strength increases with increasing anion charge density from NCS- to HO-(RO-). It is pointed out, at the same time, that the observed anion effect does not correlate with the known values of activity coefficients of the individual alkali salts which are almost insensitive to anion variation under the investigated conditions. As a resolution of the apparent paradoxon it is proposed that, in absence of the macrocyclic ligand, the stabilizing (concordant) bonding between the gegenions is nearly balanced by a destabilizing (discordant) hydrogen bonding between the ions of same charge (co-ions). Intrinsic differences among the individual salts are thus submerged in protic solvents and become apparent only when the concordant bonding is suppressed in the alkali ion-crown complex formation.


Author(s):  
Conrad H. R. Gillard ◽  
Xiuquan Zhou ◽  
Maxim Avdeev ◽  
Efrain E. Rodriguez ◽  
Neeraj Sharma
Keyword(s):  

2021 ◽  
pp. 122241
Author(s):  
Conrad Gillard ◽  
Kathleen Djohari ◽  
Partha Pratim Jana ◽  
Maxim Avdeev ◽  
Neeraj Sharma

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