Publications by authors named "Yanglansen Cui"

Biological ion channels exhibit high selectivity and permeability of ions because of their asymmetrical pore structures and surface chemistries. Here, we demonstrate a biomimetic nanofluidic channel (BNC) with an asymmetrical structure and glycyl-L-proline (GLP) -functionalization for ultrafast, selective, and unidirectional Dy extraction over other lanthanide (Ln) ions with very similar electronic configurations. The selective extraction mainly depends on the amplified chemical affinity differences between the Ln ions and GLPs in nanoconfinement.

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The quasi-solid electrolytes (QSEs) attract extensive attention due to their improved ion transport properties and high stability, which is synergistically based on tunable functional groups and confined solvent molecules among the polymetric networks. However, the trade-off effect between the polymer content and ionic conductivity exists in QSEs, limiting their rate performance. In this work, the epitaxial polymerization strategy is used to build the gradient hydrogel networks (GHNs) covalently fixed on zinc anode.

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Crystalline porous covalent frameworks (COFs) have been considered as a platform for uranium extraction from seawater and nuclear waste. However, the role of rigid skeleton and atomically precise structures of COFs is often ignored in the design of defined binding configuration. Here, a COF with an optimized relative position of two bidentate ligands realizes full potential in uranium extraction.

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Layered two-dimensional (2D) materials with interlayer channels at the nanometer scale offer an ideal platform to control ion transport behaviors, including high-precision separation, ultrafast diffusion, and tunable permeation flux, which show great potential for energy conversion and storage, water treatment, catalysis, biosynthesis, and sensing. Recent advances in controlling the structure and functionality of 2D nanofluidic channels sustainably open doors for more revolutionary applications. In this Perspective, we first present a brief introduction to the fundamental mechanisms for ion transport in 2D nanofluidic channels and an overview of state-of-the-art assembly technologies of nanochannel membranes.

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Coulombic efficiency (CE) and cycle life of metal anodes (lithium, sodium, zinc) are limited by dendritic growth and side reactions in rechargeable metal batteries. Here, we proposed a concept for constructing an anion concentration gradient (ACG)-assisted solid-electrolyte interphase (SEI) for ultrahigh ionic conductivity on metal anodes, in which the SEI layer is fabricated through an in situ chemical reaction of the sulfonic acid polymer and zinc (Zn) metal. Owing to the driving force of the sulfonate concentration gradient and high bulky sulfonate concentration, a promoted Zn ionic conductivity and inhibited anion diffusion in the SEI layer are realized, resulting in a significant suppression of dendrite growth and side reaction.

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Article Synopsis
  • High-entropy materials (HEMs) exhibit unique properties ideal for energy storage and conversion but are challenging to synthesize in atomic layers due to phase segregation.
  • Researchers successfully create high-entropy atomic layers of transition-metal carbide (HE-MXene) by selectively etching a novel HE-MAX phase, ensuring stable and homogeneous dispersion of transition metals in the layers.
  • The resulting HE-MXene demonstrates advantageous mechanical strain, which facilitates the stable growth of lithium, leading to impressive cycling stability of 1200 hours and significant efficiency in lithium stripping-plating.
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Article Synopsis
  • Single atom catalysts show improved electrocatalytic activity for chemical reactions due to better geometric and electronic structures compared to bulk catalysts.
  • Researchers developed a method to create single atom copper immobilized MXene that effectively reduces CO to methanol through selective etching of aluminum in hybrid A layers, preserving copper atoms.
  • The new single atom Cu catalyst demonstrated a high Faradaic efficiency of 59.1% for producing methanol and exhibited strong electrocatalytic stability, attributed to its unique unsaturated electronic structure which lowers energy barriers for critical reaction steps.
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