<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-20T10:22:30Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/150692" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/150692</identifier><datestamp>2023-05-16T03:00:52Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor">Ketterle, Wolfgang</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author">Park, Juliana</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Physics</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2023-05-15T19:32:48Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2023-05-15T19:32:48Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued">2023-02</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="submitted">2023-05-10T19:59:48.530Z</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/150692</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract">²³Na⁶Li is a fermionic molecule that has weak singlet-triplet mixing, making it a suitable system to study the triplet rovibrational ground state (𝑎³Σ⁺, 𝑣 = 0,𝑁 = 0). It is notable for its both non-zero electric (0.175 Debye) and magnetic (2𝜇𝐵) dipole moments and small two-body scattering rate, as predicted by the universal model for cold collision. Additionally, ²³Na⁶Li is the lightest bi-alkali molecule, and the theoretical simulation of collisions is relatively feasible compared to other heavy molecules which makes it a promising benchmark system for theoretical quantum scattering calculations. &#xd;
&#xd;
This thesis describes three experiments and a numerical/theoretical work on ²³Na⁶Li molecules in the triplet ground state. The first two experiments are on molecular Feshbach resonances: in spin-polarized ²³Na⁶Li+²³Na collisions and in ²³Na⁶Li+²³Na⁶Li collisions. The first experiment focuses on the spectroscopic study of Feshbach resonances in two possible spin-polarized ²³Na⁶Li+²³Na collisions from near 0 to 1400 Gauss. This allows learning about the molecular interaction potential surface and intermediate collision complexes, benchmarking theory, and controlling reactive collisions. The second experiment is a report of an unpredicted 𝑝-wave Feshbach resonance in ²³Na⁶Li+²³Na⁶Li collisions and interpretations. The resonance occurs for molecules in the lower stretched hyperfine state near an open-channel degeneracy. The collision loss rate is enhanced by more than two orders of magnitude from the 𝑝-wave universal value at the background to near the 2D unitarity limit.&#xd;
&#xd;
In addition to the search for magnetically tunable resonances, ²³Na⁶Li molecules in the triplet potential are suitable for magnetic trapping. The third experiment describes building an improved experimental setup that allows magnetic trapping of ²³Na⁶Li molecules and studying various collisions in the magnetic trap by quantum state control of molecules and atoms. The molecular density is a factor of 10⁵ higher than that reported for magnetically trapped ultracold molecules, and the temperature is ≈ 1𝜇𝐾. This condition enables observation of both atom-molecule and molecule-molecule collisions in the ultracold regime and sympathetic cooling of ²³Na⁶Li by evaporative cooling of ²³Na in the magnetic trap.&#xd;
&#xd;
Lastly, this thesis presents the numerical and theoretical approach to finding a window for an all-optical creation of molecules using Raman transitions from ²³Na and ⁶Li atoms to ²³Na⁶Li molecules. All-optical creation of molecules in which the magnetic association step near a Feshbach resonance is eliminated is expected to broaden the horizon of ultracold molecules to a larger pool and to eliminate the need for high magnetic fields.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="publisher">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights">In Copyright - Educational Use Permitted</dim:field>
   <dim:field mdschema="dc" element="rights">Copyright MIT</dim:field>
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   <dim:field mdschema="dc" element="title">Quantum Controlled Collisions and Magnetic Trapping of Ultracold NaLi Molecules</dim:field>
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   <dim:field mdschema="mit" element="thesis" qualifier="degree">Doctoral</dim:field>
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   	&lt;Title>Quantum Controlled Collisions and Magnetic Trapping of Ultracold NaLi Molecules&lt;/Title>
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   	&lt;PublicationDate>2023-02&lt;/PublicationDate>
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        	&lt;DisplayName>Park, Juliana&lt;/DisplayName>
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   	&lt;Abstract>²³Na⁶Li is a fermionic molecule that has weak singlet-triplet mixing, making it a suitable system to study the triplet rovibrational ground state (𝑎³Σ⁺, 𝑣 = 0,𝑁 = 0). It is notable for its both non-zero electric (0.175 Debye) and magnetic (2𝜇𝐵) dipole moments and small two-body scattering rate, as predicted by the universal model for cold collision. Additionally, ²³Na⁶Li is the lightest bi-alkali molecule, and the theoretical simulation of collisions is relatively feasible compared to other heavy molecules which makes it a promising benchmark system for theoretical quantum scattering calculations. &#xd;
&#xd;
This thesis describes three experiments and a numerical/theoretical work on ²³Na⁶Li molecules in the triplet ground state. The first two experiments are on molecular Feshbach resonances: in spin-polarized ²³Na⁶Li+²³Na collisions and in ²³Na⁶Li+²³Na⁶Li collisions. The first experiment focuses on the spectroscopic study of Feshbach resonances in two possible spin-polarized ²³Na⁶Li+²³Na collisions from near 0 to 1400 Gauss. This allows learning about the molecular interaction potential surface and intermediate collision complexes, benchmarking theory, and controlling reactive collisions. The second experiment is a report of an unpredicted 𝑝-wave Feshbach resonance in ²³Na⁶Li+²³Na⁶Li collisions and interpretations. The resonance occurs for molecules in the lower stretched hyperfine state near an open-channel degeneracy. The collision loss rate is enhanced by more than two orders of magnitude from the 𝑝-wave universal value at the background to near the 2D unitarity limit.&#xd;
&#xd;
In addition to the search for magnetically tunable resonances, ²³Na⁶Li molecules in the triplet potential are suitable for magnetic trapping. The third experiment describes building an improved experimental setup that allows magnetic trapping of ²³Na⁶Li molecules and studying various collisions in the magnetic trap by quantum state control of molecules and atoms. The molecular density is a factor of 10⁵ higher than that reported for magnetically trapped ultracold molecules, and the temperature is ≈ 1𝜇𝐾. This condition enables observation of both atom-molecule and molecule-molecule collisions in the ultracold regime and sympathetic cooling of ²³Na⁶Li by evaporative cooling of ²³Na in the magnetic trap.&#xd;
&#xd;
Lastly, this thesis presents the numerical and theoretical approach to finding a window for an all-optical creation of molecules using Raman transitions from ²³Na and ⁶Li atoms to ²³Na⁶Li molecules. All-optical creation of molecules in which the magnetic association step near a Feshbach resonance is eliminated is expected to broaden the horizon of ultracold molecules to a larger pool and to eliminate the need for high magnetic fields.&lt;/Abstract>
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