Publications by authors named "Meijuan Jia"

Biological photoresponsive ion transport systems consistently attract researchers' attention owing to their remarkable functions of harvesting energy from nature and participating in visual perception systems. Designing and constructing artificial light-driven ion transport devices to mimic biological counterparts remains a challenge owing to fabrication limitations in nanoconfined spaces. Herein, a typical conjugated polyelectrolyte (PFN-Br) was assembled onto a laminated MoSM using simple solution-processing vacuum filtration, resulting in a heterogeneous three- and two-dimensional nanoporous membrane.

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Article Synopsis
  • Biological photo-responsive ion channels are crucial for metabolic processes, and researchers aim to create artificial channels mimicking these functions using transition metal dichalcogenides for their superior properties.
  • The study introduces two specially designed peptides that functionalize WS nanosheets, creating an asymmetric peptide-WS membrane capable of photo-driven ion transport and enhancing osmotic energy conversion.
  • This new system, with its efficient design, offers a promising method for developing biomimetic ion channels applicable in areas like drug delivery, desalination, and energy conversion.
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  • Many existing bioinspired osmotic energy systems using selective membranes are not truly effective compared to biological models, particularly in generating power with specific ionic channels.
  • Researchers developed a K-channel using a special K-selective ligand and graphene oxide membrane, achieving a high selectivity ratio for potassium over sodium.
  • The newly constructed K-selective iso-osmotic power generator (KSIPG) demonstrated a power density of about 15.1 mW/m, outperforming traditional methods and suggesting potential applications in various fields like self-powered systems and medical technology.
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Bioinspired two-dimensional (2D) nanofluidic systems for photo-induced ion transport have attracted great attention, as they open a new pathway to enabling light-to-ionic energy conversion. However, there is still a great challenge in achieving a satisfactory performance. It is noticed that organic solar cells (OSCs, light-harvesting device based on photovoltaic effect) commonly require hole/electron transport layer materials (TLMs), PEDOT:PSS (PE) and PDINN (PD), respectively, to promote the energy conversion.

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Light-driven proton directional transport is important in living beings as it could subtly realize the light energy conversion for living uses. In the past years, 2D materials-based nanochannels have shown great potential in active ion transport due to controllable properties, including surface charge distribution, wettability, functionalization, electric structure, and external stimuli responsibility, etc. However, to fuse the inorganic materials into bio-membranes still faces several challenges.

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Nanofluidic ion transport through van der Waals heterostructures, composed of two or more types of reconstructed 2D nanomaterials, gives rise to fascinating opportunities for light-energy harvesting, due to coupling between the optoelectronic properties of the layered constituents and ion transport in between the atomic layers. Here, a photoinduced active ion transport phenomenon through transition metal dichalcogenides (TMDs)-based van-der-Waals-like multilayer heterostructures is reported for harnessing ionic power from equilibrium electrolyte solution. The binary heterostructure comprises sequentially stacked 2D-WS and 2D-MoS multilayers with sub-1 nm interlayer spacing.

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Nacre-mimetic 2D nanofluidic materials with densely packed sub-nanometer-height lamellar channels find widespread applications in water-, energy-, and environment-related aspects by virtue of their scalable fabrication methods and exceptional transport properties. Recently, light-powered nanofluidic ion transport in synthetic materials gained considerable attention for its remote, noninvasive, and active control of the membrane transport property using the energy of light. Toward practical application, a critical challenge is to overcome the dependence on inhomogeneous or site-specific light illumination.

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Biological electrogenic systems use protein-based ionic pumps to move salt ions uphill across a cell membrane to accumulate an ion concentration gradient from the equilibrium physiological environment. Toward high-performance and robust artificial electric organs, attaining an antigradient ion transport mode by fully abiotic materials remains a great challenge. Herein, a light-driven proton pump transport phenomenon through a Janus graphene oxide membrane (JGOM) is reported.

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The bottom-up assembly of ion-channel-mimetic nanofluidic devices and materials with two-dimensional (2D) nano-building blocks paves a straightforward way towards the real-world applications of the novel transport phenomena on a nano- or sub-nanoscale. One immediate challenge is to provide the 2D nanofluidic systems with adaptive responsibilities and asymmetric ion transport characteristics. Herein, we introduce a facile and general strategy to provide a graphene-oxide-based 2D nanofluidic system with photo-switchable ionic current rectification (ICR).

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