News Release

Multiscale theoretical calculations empower robust electric double layer toward highly reversible zinc anode

Peer-Reviewed Publication

Shanghai Jiao Tong University Journal Center

Multiscale Theoretical Calculations Empower Robust Electric Double Layer Toward Highly Reversible Zinc Anode

image: 

  • A multiscale theoretical framework deciphers the molecular-ionic dynamics of the electric double layer (EDL) in aqueous rechargeable zinc batteries, correlating interfacial water aggregation, anion-specific adsorption, and electric field inhomogeneity to parasitic reactions and dendrite growth, thereby establishing EDL-driven design principles for ultra-stable Zn anodes.
  • Molecular adsorption engineering creates a localized “water-poor and anion-expelled” EDL configuration that suppresses hydrogen evolution and by-product formation while enabling dense Zn electrodeposition through flattened interfacial potential gradients and reduced Zn2+ electrostatic repulsion.
view more 

Credit: Yufan Xia, Zhen Luo, Shuang Chen, Yang Xiang, Gao Weng, Hongge Pan, Ben Bin Xu, Mi Yan, Yinzhu Jiang*.

As aqueous rechargeable zinc batteries (ARZBs) edge closer to grid-scale deployment, the zinc metal anode remains dogged by dendrite proliferation and parasitic hydrogen evolution that slash cycle life and safety. Now, researchers from Zhejiang University, led by Prof. Yinzhu Jiang, have delivered a multiscale theoretical-experimental blueprint that deciphers and tames the electric double layer (EDL) at the zinc-electrolyte interface. The work, published in Nano-Micro Letters, introduces a low-cost sugar-derivative additive that rewrites interfacial chemistry, pushing Zn||Zn symmetric cells beyond 4 700 h and full cells to >90 % capacity retention after 800 cycles.

Why the EDL Matters

  • Reaction Gatekeeper: The EDL controls ion flux, charge distribution and nucleation thermodynamics—yet classical mean-field models ignore molecular-scale heterogeneity.
  • Water-Induced Failures: Water-rich inner Helmholtz planes trigger hydrogen evolution and insulating Zn4SO4(OH)6·xH2O by-products.
  • Theory-Experiment Gap: Ab-initio or continuum methods alone cannot capture dynamic ion/molecule reorganization under battery-operating conditions.

Innovative Multiscale Framework

  • QC-DFT-CMD Pipeline: Quantum-chemistry pinpoints adsorption sites, DFT quantifies energetics, and constant-potential classical MD maps real-time EDL restructuring.
  • Additive Design Rules: 4,1′,6′-trichlorogalactosucrose (TGS) is selected for its bulky chlorinated skeleton and abundant –OH anchors that self-assemble into a “water-poor & anion-expelled” EDL.
  • Steric-Plus-Electronic Effect: TGS parallel adsorption (−0.97 eV) displaces 94 % of surface water and expels SO42- from the Helmholtz region, flattening interfacial potential gradients.

Performance Breakthroughs

  • Anti-Corrosion: HER barrier rises from 0.69 to 0.84 eV; corrosion current plummets from 4.64 to 0.86 mA cm-2.
  • Dendrite Suppression: Overpotential increase enforces 3D diffusion-limited deposition, yielding dense (002)-textured plates instead of mossy or dendritic grains.
  • Long-Term Stability: Zn||Cu cells deliver 99.5 % CE over 1 100 cycles; Zn||NaV3O8·1.5H₂O pouch cells retain 71.8 % capacity after 50 cycles at 2 mA cm-2.

Future Outlook
The study establishes a transferable platform for additive-guided EDL engineering, opening a general pathway toward ultra-stable metal anodes beyond zinc.


Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.