Lanthanide-Containing Functional Materials - From Molecular Level to Bulk Level

Persistent Link:
http://hdl.handle.net/10150/613124
Title:
Lanthanide-Containing Functional Materials - From Molecular Level to Bulk Level
Author:
Zhang, Zhonghao
Issue Date:
2016
Publisher:
The University of Arizona.
Rights:
Copyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
Abstract:
This work is a comprehensive summary of research projects the author conducted when attending the PhD program at the University of Arizona. Research topics cover the structural chemistry of lanthanide-amino-acid clusters, optical up-conversion properties of lanthanide based nanomaterials, magnetic and luminescent properties of lanthanide metal-organic frameworks (MOFs), as well as two research projects focusing on transition metal MOFs, which were derived from lanthanide metal-organic framework projects. In chapter 2, the discovery of halide anion templated lanthanide-histidine hydroxide cluster and a comprehensive study of the influence of anionic size on cluster nuclearity are discussed. Both Cl⁻ and Br⁻ were able to serve as template anions assisting the formation of pentadeca-nuclear lanthanide hydroxide clusters for Nd, Gd and Er. When I⁻ was used as the template anion, pentadeca-nuclear hydroxide cluster only formed in neodymium case. In erbium case a dodeca-nuclear hydroxide cluster formed when I⁻ was used as template ion. However I⁻ was not effective in assisting the formation of high nuclearity gadolinium hydroxide cluster. In chapter 3, doping Er³⁺ ion into CuₓSe nanoparticles for the purpose of making efficient optical up-conversion materials is discussed. Er³⁺ ion was successfully doped into CuₓSe nanoparticles. However no up-conversion luminescence was detected, possibly due to the in-direct bandgap nature of CuₓSe. Chapter 4 discuses attaching CuxSe nanoparticles on the surface of NaYF₄:Gd, Er,Yb nanorod. The purpose is to increase up-conversion efficiency of NaYF₄:Gd, Er,Yb nanorod through surface plasmon resonance enhancement property of CuₓSe nanoparticle. The CuₓSe nanoparticles were successfully attached onto NaYF₄:Gd, Er,Yb nanorod surface through exposing the suspension containing CuₓSe nanoparticles and NaYF₄:Gd, Er,Yb nanorods to UV irradiation. The up-conversion efficiency of NaYF₄:Gd, Er,Yb nanorods was increased after CuₓSe nanoparticle attachment. Chapter 5 discussed the synthesis and characterization of functional Ln(BDC)(1.5)∙DMF (Ln = Eu, Tb, Gd) metal-organic frameworks (MOFs). The absence of OH group containing species within this MOF rendered them ideal substrates as luminescent material because luminescence quenching caused by OH groups could be avoided. A series of MOF with luminescent color ranging from red, orange, yellow and green were obtained by adjusting the relative Eu and Tb content in the MOF lattice. The magnetocaloric effect of Gd(BDC)1.5∙DMF was also studied. Chapter 6 discussed doping Co²⁺ ion into pyrochlore-like Zn(INA)₂ (INA = isonicotinate) MOF lattice for the purpose of making magnetically active pyrochlore-like MOF structures. The highest Co²⁺ doping concentration of 57% was successfully achieved. However, no significant magnetic frustration was observed, possibly due to the far separation between doped Co²⁺ ions. Chapter 7 discussed the etching of Zn(INA)₂ MOF crystal to increase microporous exposure. When Zn(INA)₂ MOF crystals were immersed in Co(NO₃)₂∙6H₂O acetonitrile solution, defined effective etching, which could effectively increase microporous exposure, took place. When Zn(INA)₂ MOF crystals were immersed in Co(NO₃)₂∙6H₂O N,N-dimethylformamide solution, defined ineffective etching, which could not increase microporous exposure, took place dominantly. Increasing etching temperature resulted in similar but more severe etching. However, new cobalt dominant MOF phases formed when etching was performed under elevated temperature.
Type:
text; Electronic Dissertation
Keywords:
Chemistry
Degree Name:
Ph.D.
Degree Level:
doctoral
Degree Program:
Graduate College; Chemistry
Degree Grantor:
University of Arizona
Advisor:
Zheng, Zhiping

Full metadata record

DC FieldValue Language
dc.language.isoen_USen
dc.titleLanthanide-Containing Functional Materials - From Molecular Level to Bulk Levelen_US
dc.creatorZhang, Zhonghaoen
dc.contributor.authorZhang, Zhonghaoen
dc.date.issued2016-
dc.publisherThe University of Arizona.en
dc.rightsCopyright © is held by the author. Digital access to this material is made possible by the University Libraries, University of Arizona. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.en
dc.description.abstractThis work is a comprehensive summary of research projects the author conducted when attending the PhD program at the University of Arizona. Research topics cover the structural chemistry of lanthanide-amino-acid clusters, optical up-conversion properties of lanthanide based nanomaterials, magnetic and luminescent properties of lanthanide metal-organic frameworks (MOFs), as well as two research projects focusing on transition metal MOFs, which were derived from lanthanide metal-organic framework projects. In chapter 2, the discovery of halide anion templated lanthanide-histidine hydroxide cluster and a comprehensive study of the influence of anionic size on cluster nuclearity are discussed. Both Cl⁻ and Br⁻ were able to serve as template anions assisting the formation of pentadeca-nuclear lanthanide hydroxide clusters for Nd, Gd and Er. When I⁻ was used as the template anion, pentadeca-nuclear hydroxide cluster only formed in neodymium case. In erbium case a dodeca-nuclear hydroxide cluster formed when I⁻ was used as template ion. However I⁻ was not effective in assisting the formation of high nuclearity gadolinium hydroxide cluster. In chapter 3, doping Er³⁺ ion into CuₓSe nanoparticles for the purpose of making efficient optical up-conversion materials is discussed. Er³⁺ ion was successfully doped into CuₓSe nanoparticles. However no up-conversion luminescence was detected, possibly due to the in-direct bandgap nature of CuₓSe. Chapter 4 discuses attaching CuxSe nanoparticles on the surface of NaYF₄:Gd, Er,Yb nanorod. The purpose is to increase up-conversion efficiency of NaYF₄:Gd, Er,Yb nanorod through surface plasmon resonance enhancement property of CuₓSe nanoparticle. The CuₓSe nanoparticles were successfully attached onto NaYF₄:Gd, Er,Yb nanorod surface through exposing the suspension containing CuₓSe nanoparticles and NaYF₄:Gd, Er,Yb nanorods to UV irradiation. The up-conversion efficiency of NaYF₄:Gd, Er,Yb nanorods was increased after CuₓSe nanoparticle attachment. Chapter 5 discussed the synthesis and characterization of functional Ln(BDC)(1.5)∙DMF (Ln = Eu, Tb, Gd) metal-organic frameworks (MOFs). The absence of OH group containing species within this MOF rendered them ideal substrates as luminescent material because luminescence quenching caused by OH groups could be avoided. A series of MOF with luminescent color ranging from red, orange, yellow and green were obtained by adjusting the relative Eu and Tb content in the MOF lattice. The magnetocaloric effect of Gd(BDC)1.5∙DMF was also studied. Chapter 6 discussed doping Co²⁺ ion into pyrochlore-like Zn(INA)₂ (INA = isonicotinate) MOF lattice for the purpose of making magnetically active pyrochlore-like MOF structures. The highest Co²⁺ doping concentration of 57% was successfully achieved. However, no significant magnetic frustration was observed, possibly due to the far separation between doped Co²⁺ ions. Chapter 7 discussed the etching of Zn(INA)₂ MOF crystal to increase microporous exposure. When Zn(INA)₂ MOF crystals were immersed in Co(NO₃)₂∙6H₂O acetonitrile solution, defined effective etching, which could effectively increase microporous exposure, took place. When Zn(INA)₂ MOF crystals were immersed in Co(NO₃)₂∙6H₂O N,N-dimethylformamide solution, defined ineffective etching, which could not increase microporous exposure, took place dominantly. Increasing etching temperature resulted in similar but more severe etching. However, new cobalt dominant MOF phases formed when etching was performed under elevated temperature.en
dc.typetexten
dc.typeElectronic Dissertationen
dc.subjectChemistryen
thesis.degree.namePh.D.en
thesis.degree.leveldoctoralen
thesis.degree.disciplineGraduate Collegeen
thesis.degree.disciplineChemistryen
thesis.degree.grantorUniversity of Arizonaen
dc.contributor.advisorZheng, Zhipingen
dc.contributor.committeememberLichtenberger, Dennis L.en
dc.contributor.committeememberLoy, Dougen
dc.contributor.committeememberTomat, Elisaen
dc.contributor.committeememberZheng, Zhipingen
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