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Experimental and Computational Study of Electrides With Unique Dimensionality and Metastability: A 3D Electride and an Emerging Class of Dynamically Stable Electrides
Experimental and Computational Study of Electrides With Unique Dimensionality and Metastab...
Experimental and Computational Study of Electrides With Unique Dimensionality and Metastability: A 3D Electride and an Emerging Class of Dynamically Stable Electrides

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자료유형  
 학위논문 서양
최종처리일시  
20260202103127
ISBN  
9798315712053
DDC  
546
저자명  
Lanetti, Matthew Gordon.
서명/저자  
Experimental and Computational Study of Electrides With Unique Dimensionality and Metastability: A 3D Electride and an Emerging Class of Dynamically Stable Electrides
발행사항  
[Sl] : The University of North Carolina at Chapel Hill, 2025
발행사항  
Ann Arbor : ProQuest Dissertations & Theses, 2025
형태사항  
174 p
주기사항  
Source: Dissertations Abstracts International, Volume: 86-11, Section: B.
주기사항  
Advisor: Cahoon, James F.;Erie, Dorothy A.
학위논문주기  
Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2025.
초록/해제  
요약This work details novel electrides, new chemistries toward their synthesis, their unique applications in ion storage, and computational simulation of these materials. Electrides with unique dimensionality and topology, particularly three-dimensional (3D) and two-dimensional (2D) electride gases, are explored.I achieve a high-purity synthesis of Ti2C and demonstrate it to be one of the first 3D electrides. A comprehensive analysis of density functional theory (DFT) calculations, experimental diffraction, spectroscopic data, and prior claims is used to convincingly solve the decades-long debate over the crystal structure of Ti2C. These results indicate that the carbon positions in this material pattern in a 3D structure, with the carbon vacancies adopting an identical pattern, which is best described as diamond cubic. DFT calculations demonstrate that electride electrons occupy the carbon vacancies of this material, revealing it to be among the first 3D electrides. I show that Ti2C is a bicontinuous material consisting of a continuous diamond-cubic crystal structure interpenetrating a continuous symmetrical 3D electride structure. I exploit the electride sites in a hydrogenation of Ti2C, demonstrating potential application of this material in ion storage. This ion-insertion reaction proceeds via the direct substitution of hydride for electride electrons- an electron-anion exchange (EAX) reaction. I explore the use of the EAX reaction as a synthetic means toward novel electrides. I identify how EAX can be used to produce electrides in a kinetically controlled reaction to achieve electrides not limited to thermodynamic products. I use DFT to support my hypothesis that EAX can enable access to metastable electrides, a synthetic target not previously explored. In this study I identify possibly the first-known dynamically-stable electride structures including a new class of metastable 2D electrides related to the well-studied LaOAgS structure type.
일반주제명  
Inorganic chemistry
일반주제명  
Physical chemistry
일반주제명  
Materials science
일반주제명  
Computational chemistry
키워드  
Diffraction
키워드  
Electrides
키워드  
Ion storage
키워드  
Synthesis
키워드  
Titanium
키워드  
Topology
기타저자  
The University of North Carolina at Chapel Hill Chemistry
기본자료저록  
Dissertations Abstracts International. 86-11B.
전자적 위치 및 접속  
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MARC

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■020    ▼a9798315712053
■035    ▼a(MiAaPQ)AAI31938897
■040    ▼aMiAaPQ▼cMiAaPQ
■0820  ▼a546
■1001  ▼aLanetti,  Matthew  Gordon.
■24510▼aExperimental  and  Computational  Study  of  Electrides  With  Unique  Dimensionality  and  Metastability:  A  3D  Electride  and  an  Emerging  Class  of  Dynamically  Stable  Electrides
■260    ▼a[Sl]▼bThe  University  of  North  Carolina  at  Chapel  Hill▼c2025
■260  1▼aAnn  Arbor▼bProQuest  Dissertations  &  Theses▼c2025
■300    ▼a174  p
■500    ▼aSource:  Dissertations  Abstracts  International,  Volume:  86-11,  Section:  B.
■500    ▼aAdvisor:  Cahoon,  James  F.;Erie,  Dorothy  A.
■5021  ▼aThesis  (Ph.D.)--The  University  of  North  Carolina  at  Chapel  Hill,  2025.
■520    ▼aThis  work  details  novel  electrides,  new  chemistries  toward  their  synthesis,  their  unique  applications  in  ion  storage,  and  computational  simulation  of  these  materials.  Electrides  with  unique  dimensionality  and  topology,  particularly  three-dimensional  (3D)  and  two-dimensional  (2D)  electride  gases,  are  explored.I  achieve  a  high-purity  synthesis  of  Ti2C  and  demonstrate  it  to  be  one  of  the  first  3D  electrides.  A  comprehensive  analysis  of  density  functional  theory  (DFT)  calculations,  experimental  diffraction,  spectroscopic  data,  and  prior  claims  is  used  to  convincingly  solve  the  decades-long  debate  over  the  crystal  structure  of  Ti2C.  These  results  indicate  that  the  carbon  positions  in  this  material  pattern  in  a  3D  structure,  with  the  carbon  vacancies  adopting  an  identical  pattern,  which  is  best  described  as  diamond  cubic.  DFT  calculations  demonstrate  that  electride  electrons  occupy  the  carbon  vacancies  of  this  material,  revealing  it  to  be  among  the  first  3D  electrides.  I  show  that  Ti2C  is  a  bicontinuous  material  consisting  of  a  continuous  diamond-cubic  crystal  structure  interpenetrating  a  continuous  symmetrical  3D  electride  structure.  I  exploit  the  electride  sites  in  a  hydrogenation  of  Ti2C,  demonstrating  potential  application  of  this  material  in  ion  storage.  This  ion-insertion  reaction  proceeds  via  the  direct  substitution  of  hydride  for  electride  electrons-  an  electron-anion  exchange  (EAX)  reaction. I  explore  the  use  of  the  EAX  reaction  as  a  synthetic  means  toward  novel  electrides.  I  identify  how  EAX  can  be  used  to  produce  electrides  in  a  kinetically  controlled  reaction  to  achieve  electrides  not  limited  to  thermodynamic  products.  I  use  DFT  to  support  my  hypothesis  that  EAX  can  enable  access  to  metastable  electrides,  a  synthetic  target  not  previously  explored.  In  this  study  I  identify  possibly  the  first-known  dynamically-stable  electride  structures  including  a  new  class  of  metastable  2D  electrides  related  to  the  well-studied  LaOAgS  structure  type.
■590    ▼aSchool  code:  0153.
■650  4▼aInorganic  chemistry
■650  4▼aPhysical  chemistry
■650  4▼aMaterials  science
■650  4▼aComputational  chemistry
■653    ▼aDiffraction
■653    ▼aElectrides
■653    ▼aIon  storage
■653    ▼aSynthesis
■653    ▼aTitanium
■653    ▼aTopology
■690    ▼a0794
■690    ▼a0488
■690    ▼a0494
■690    ▼a0219
■71020▼aThe  University  of  North  Carolina  at  Chapel  Hill▼bChemistry.
■7730  ▼tDissertations  Abstracts  International▼g86-11B.
■790    ▼a0153
■791    ▼aPh.D.
■792    ▼a2025
■793    ▼aEnglish
■85640▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T17357074▼nKERIS▼z이  자료의  원문은  한국교육학술정보원에서  제공합니다.

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