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        <identifier>oai:figshare.com:article/34054854</identifier>
        <datestamp>2026-10-02T05:43:59Z</datestamp>
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          <dc:title>Data Sheet 1_Adsorption-dominated interfacial regulation by sarcosine via hydrogen-bond water modulation for stable Zn metal anodes.pdf</dc:title>
          <dc:creator>Zijing Wang (3090645)</dc:creator>
          <dc:creator>Haolin Ju (25162875)</dc:creator>
          <dc:creator>Hao Zhang (15339)</dc:creator>
          <dc:creator>Yiqian Yang (13000827)</dc:creator>
          <dc:creator>Huan Liu (281351)</dc:creator>
          <dc:creator>Bin Cao (186972)</dc:creator>
          <dc:creator>Jie Ding (73711)</dc:creator>
          <dc:creator>Bin Xu (10691)</dc:creator>
          <dc:subject>Organic Chemistry</dc:subject>
          <dc:subject>adsorption</dc:subject>
          <dc:subject>aqueous zinc-ion batteries</dc:subject>
          <dc:subject>hydrogen-bond water regulation</dc:subject>
          <dc:subject>sarcosine</dc:subject>
          <dc:subject>zn metal anode</dc:subject>
          <dc:description>&lt;p&gt;Aqueous zinc-ion batteries (AZIBs) hold great promise for safe and low‐cost energy storage, yet their practical application is seriously hindered by the hydrogen evolution reaction (HER), uncontrolled dendrite growth, and inert byproduct (Zn4SO4(OH)6·xH2O) deposition on the Zn anode. In this work, sarcosine (Sar) was adopted as a multifunctional bipolar electrolyte additive, and first‐principles calculations combined with electrochemical tests and interfacial characterizations were performed to reveal its adsorption‐dominated interfacial stabilization mechanism. Sar strongly adsorbs on the Zn surface to homogenize Zn2+ flux, regulate the electric field distribution, and reconfigure the interfacial environment. Meanwhile, Sar forms strong intermolecular hydrogen bonds with water molecules via its amino and carboxyl groups, reducing free water activity and suppressing HER. First‐principles calculations verify the favorable adsorption configuration and high adsorption energy of Sar on the Zn surface. As a result, the Zn||Zn symmetric cell delivers ultra‐long cycling stability over 2100 h at 1 mA cm‐2, and the Zn||Cu half‐cell exhibits a high average Coulombic efficiency of 99.7%. The full cell with ZnI@CNT‐AC cathode maintains excellent capacity retention after 3000 cycles. This work provides a simple, green, and low‐cost strategy for stabilizing Zn anodes toward practical aqueous zinc‐ion batteries.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-02T05:43:59Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fchem.2026.1986660.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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