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        <datestamp>2026-09-29T18:05:55Z</datestamp>
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        <oai_dc:dc xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"  xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
          <dc:title>Understanding Mass Transport and Reaction Environment
to Optimize CO&lt;sub&gt;2&lt;/sub&gt; Electrodialysis Systems</dc:title>
          <dc:creator>Jintong Gao (21628397)</dc:creator>
          <dc:creator>Yusaku Nishimura (25138496)</dc:creator>
          <dc:creator>Gong Zhang (69122)</dc:creator>
          <dc:creator>Tsuyoshi Hamaguchi (396045)</dc:creator>
          <dc:creator>Masaoki Iwasaki (6597356)</dc:creator>
          <dc:creator>Lenan Zhang (5546309)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Space Science</dc:subject>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Evolutionary Biology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>electrodialysis systems electrodialysis</dc:subject>
          <dc:subject>direct air capture</dc:subject>
          <dc:subject>although previous studies</dc:subject>
          <dc:subject>understanding mass transport</dc:subject>
          <dc:subject>coupled mass transport</dc:subject>
          <dc:subject>proton utilization efficiency</dc:subject>
          <dc:subject>informed design insights</dc:subject>
          <dc:subject>efficient carbon utilization</dc:subject>
          <dc:subject>bubble nucleation barrier</dc:subject>
          <dc:subject>2 &lt;/ sub</dc:subject>
          <dc:subject>significantly advanced co</dc:subject>
          <dc:subject>bubble nucleation</dc:subject>
          <dc:subject>providing transport</dc:subject>
          <dc:subject>mechanistic insights</dc:subject>
          <dc:subject>current efficiency</dc:subject>
          <dc:subject>efficient co</dc:subject>
          <dc:subject>system levels</dc:subject>
          <dc:subject>specific trade</dc:subject>
          <dc:subject>renewable electricity</dc:subject>
          <dc:subject>reaction zones</dc:subject>
          <dc:subject>reaction localization</dc:subject>
          <dc:subject>reaction environment</dc:subject>
          <dc:subject>ph gradient</dc:subject>
          <dc:subject>operating conditions</dc:subject>
          <dc:subject>generation rate</dc:subject>
          <dc:subject>critical technology</dc:subject>
          <dc:subject>approach captures</dc:subject>
          <dc:description>Electrodialysis
(ED) is a critical technology for decarbonization,
which can be paired with direct air capture to produce a concentrated
CO&lt;sub&gt;2&lt;/sub&gt; stream for efficient carbon utilization and storage.
Although previous studies have significantly advanced CO&lt;sub&gt;2&lt;/sub&gt; ED at the process, membrane, and system levels, the coupled mass
transport and reaction environment governing CO&lt;sub&gt;2&lt;/sub&gt; regeneration
remain insufficiently understood, limiting further improvement in
current efficiency. Here we develop a spatially resolved modeling
framework for CO&lt;sub&gt;2&lt;/sub&gt; ED. Our approach captures the interplay
among concentration polarization, pH gradient, and reaction localization,
thereby enabling direct prediction of CO&lt;sub&gt;2&lt;/sub&gt; generation rate,
proton utilization efficiency, and bubble nucleation barrier. Using
three representative electrolytes with distinct acid–base properties,
we show that buffering and acidity can substantially reshape ion distributions
and reaction zones, which produce electrolyte-specific trade-offs
between CO&lt;sub&gt;2&lt;/sub&gt; regeneration and bubble nucleation. Building
on these mechanistic insights, we further identify ED cell geometries
and operating conditions that maximize proton utilization efficiency
while mitigating undesirable bubble nucleation. This work elucidates
mass transport and reaction environment in CO&lt;sub&gt;2&lt;/sub&gt; ED, providing
transport-informed design insights for efficient CO&lt;sub&gt;2&lt;/sub&gt; regeneration
powered by renewable electricity.</dc:description>
          <dc:date>2026-09-29T00:00:00Z</dc:date>
          <dc:type>Text</dc:type>
          <dc:type>Journal contribution</dc:type>
          <dc:identifier>10.1021/acsestengg.6c00435.s001</dc:identifier>
          <dc:relation>https://figshare.com/articles/journal_contribution/Understanding_Mass_Transport_and_Reaction_Environment_to_Optimize_CO_sub_2_sub_Electrodialysis_Systems/34027202</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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