Hydrogen‑Bonded Interfacial Super‑Assembly of Spherical Carbon Superstructures for High‑Performance Zinc Hybrid Capacitors

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Hydrogen‑Bonded Interfacial Super‑Assembly of Spherical Carbon Superstructures for High‑Performance Zinc Hybrid Capacitors
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Hydrogen-Bonded Interfacial Super-Assembly of Spherical Carbon Superstructures for High-Performance Zinc Hybrid Capacitors - Nano-Micro Letters

Carbon superstructures with multiscale hierarchies and functional attributes represent an appealing cathode candidate for zinc hybrid capacitors, but their tailor-made design to optimize the capacitive activity remains a confusing topic. Here we develop a hydrogen-bond-oriented interfacial super-assembly strategy to custom-tailor nanosheet-intertwined spherical carbon superstructures (SCSs) for Zn-ion storage with double-high capacitive activity and durability. Tetrachlorobenzoquinone (H-bond acceptor) and dimethylbenzidine (H-bond donator) can interact to form organic nanosheet modules, which are sequentially assembled, orientally compacted and densified into well-orchestrated superstructures through multiple H-bonds (N–H···O). Featured with rich surface-active heterodiatomic motifs, more exposed nanoporous channels, and successive charge migration paths, SCSs cathode promises high accessibility of built-in zincophilic sites and rapid ion diffusion with low energy barriers (3.3 Ω s−0.5). Consequently, the assembled Zn||SCSs capacitor harvests all-round improvement in Zn-ion storage metrics, including high energy density (166 Wh kg−1), high-rate performance (172 mAh g−1 at 20 A g−1), and long-lasting cycling lifespan (95.5% capacity retention after 500,000 cycles). An opposite charge-carrier storage mechanism is rationalized for SCSs cathode to maximize spatial capacitive charge storage, involving high-kinetics physical Zn2+/CF3SO3− adsorption and chemical Zn2+ redox with carbonyl/pyridine groups. This work gives insights into H-bond-guided interfacial super-assembly design of superstructural carbons toward advanced energy storage.

As the demand for high-performance energy storage systems intensifies, aqueous zinc-ion hybrid capacitors (ZHCs) have emerged as a promising technology due to their high safety, low cost, and environmental friendliness. Now, researchers from Tongji University, led by Prof. Ziyang Song and Prof. Lihua Gan, have developed a novel hydrogen-bond-guided interfacial super-assembly strategy to construct spherical carbon superstructures (SCS-6) with exceptional energy storage performance. This work offers valuable insights into the design of advanced carbon cathodes for next-generation energy storage.

Why Spherical Carbon Superstructures Matter

  • Ultrahigh Energy Density: The SCS-6 cathode delivers an outstanding energy density of 166 Wh kg-1, outperforming most reported carbon-based ZHCs.
  • Ultra-Long Cycle Life: The Zn||SCS-6 device maintains 95.5% capacity retention after 500,000 cycles, demonstrating exceptional durability.
  • Fast Ion Transport: Unique surface-opening pores and interconnected channels enable rapid Zn2+ diffusion and high-rate performance.
  • Dual-Ion Storage Mechanism: A proton-assisted opposite charge-carrier storage mechanism maximizes spatial charge utilization and boosts capacity.

Innovative Design and Features

  • Hydrogen-Bond-Driven Assembly:
    Tetrachlorobenzoquinone (H-bond acceptor) and dimethylbenzidine (H-bond donor) self-assemble into 2D nanosheet modules, which are then compacted into 3D spherical superstructures via N–H···O hydrogen bonding.
  • Hierarchical Porous Architecture:
    The resulting SCS-6 features micropores (~0.8 nm) and mesopores (2–12 nm), with a specific surface area of 2530 m2 g-1, ensuring high accessibility of active sites and efficient electrolyte infiltration.
  • Rich Heteroatom Doping:
    N/O co-doping introduces zincophilic sites (e.g., carbonyl, pyridine groups) that enhance Zn2+ adsorption and redox activity.

Applications and Future Outlook

  • High-Performance Zn-Ion Hybrid Capacitors:
    The Zn||SCS-6 device achieves 246 mAh g-1 at 0.2 A g-1 and 172 mAh g-1 at 20 A g-1, with 99.8% Coulombic efficiency over half a million cycles.
  • Proton-Assisted Charge Storage:
    A dual-ion mechanism involving Zn2+/H+ co-storage via physical adsorption and chemical redox reactions significantly enhances capacity and kinetics.
  • Scalable and Tunable Synthesis:
    The solvent-adaptable super-assembly process enables morphology control (e.g., flower-like, curly flake), offering flexibility for diverse energy storage applications.
  • Challenges and Opportunities:
    Future research will focus on mass-loading scalability, electrolyte optimization, and mechanical flexibility for wearable and grid-scale energy systems.

This comprehensive study provides a roadmap for hydrogen-bond-guided carbon superstructure design, highlighting the importance of interfacial engineering, hierarchical porosity, and heteroatom doping in advancing high-energy, long-life energy storage technologies.

Stay tuned for more groundbreaking work from Prof. Ziyang Song and Prof. Lihua Gan at Tongji University!

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Nanomaterial
Physical Sciences > Physics and Astronomy > Condensed Matter Physics > Nanophysics > Nanomaterial
Supercapacitors
Physical Sciences > Materials Science > Materials for Energy and Catalysis > Supercapacitors
Carbon Materials
Physical Sciences > Chemistry > Materials Chemistry > Carbon Materials
  • Nano-Micro Letters Nano-Micro Letters

    Nano-Micro Letters is a peer-reviewed, international, interdisciplinary and open-access journal that focus on science, experiments, engineering, technologies and applications of nano- or microscale structure and system in physics, chemistry, biology, material science, and pharmacy.