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    <identifier>10.57760/sciencedb.34555</identifier>
    <datestamp>2025-12-30T16:57:02Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-12-30</dc:date>
  <dc:title>Metal Identity as a Design Switch: Engineering Salt Adaptive Photothermal Evaporation in Conjugated Metal-organic Frameworks</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.34555</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Photothermal interfacial evaporation represents a promising route to address global water scarcity, yet achieving simultaneously high efficiency and robust salt tolerance remains a critical challenge. The decisive role of the metal center in governing the hierarchical architecture and evaporation dynamics of metal&amp;ndash;organic frameworks (MOFs), especially in saline environments, remains underexplored, despite their versatile, tunable structures for interfacial design. Herein, using a scalable series of two-dimensional conjugated M&amp;ndash;HITP frameworks, we demonstrate that metal identity acts as a central design switch to direct coordination geometry, long-range order, and ultimately, photothermal performance. While all M&amp;ndash;HITP variants exhibit exceptional solar evaporation rates that surpass conventional systems, only Ni&amp;ndash;HITP displays a distinctive salt-adaptive enhancement, with its evaporation rate rising from 3.28 kg&amp;middot;m&amp;ndash;2&amp;middot;h&amp;ndash;1 in pure water to 4.80 kg&amp;middot;m&amp;ndash;2&amp;middot;h&amp;ndash;1 in 3.5 wt% NaCl. This unique behavior originates from the strong metal&amp;ndash;ligand coupling and highly ordered layered structure, which promotes selective salt-ion enrichment at the evaporation interface. Such interfacial ion accumulation reconstructs the hydrogen-bond network of water, significantly reducing the effective evaporation enthalpy from 667.43 J&amp;middot;g&amp;ndash;1 to 424.04 J&amp;middot;g&amp;ndash;1. This work not only deciphers the metal center structure performance interplay in conjugated MOFs but also establishes a novel salt-utilization strategy, paving a rational design pathway toward adaptive, high-performance photothermal evaporators for real-world saline water treatment.</dc:description>
  <dc:subject>Metal-organic frameworks; salt-enhanced evaporation; hydrogen-bond network; solar thermal; enthalpy</dc:subject>
  <dc:creator>Fenghua Liu</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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