Publications by authors named "Maobin Pang"

Article Synopsis
  • Efficient conduction of hydroxide ions (OH) in anion exchange membranes (AEMs) is crucial for improving sustainable technologies like water electrolysis and fuel cells.
  • Researchers developed innovative AEMs with rigid, heteroatom-free micropores engineered for fast and stable ionic transport, resulting in a significant increase in conductivity and durability.
  • These new membranes not only improve energy efficiency and lifespan, but also allow for the use of less expensive catalysts, making them promising for future advancements in electrochemical applications.
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Fabrication of ion-conducting membranes with continuous sub-nanometer channels holds fundamental importance for flow batteries in achieving safe integration of renewable energy into grids. Self-standing covalent organic polymer (COP) membranes provide feasibility due to their rapid and selective ion transport. However, the development of a scale-up possible, mechanically robust and chemically stable membranes remains a significant challenge.

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Developing a high-efficiency and stable anode catalyst layer (CL) is crucial for promoting the practical applications of anion exchange membrane (AEM) water electrolyzers. Herein, a hierarchical nanosheet array composed of oxygen vacancy-enriched CoCrO nanosheets and dispersed FeNi layered double hydroxide (LDH) is proposed to regulate the electronic structure and increase the electrical conductivity for improving the intrinsic activity of the oxygen evolution reaction (OER). The CoCrO/NiFe LDH electrodes require an overpotential of 205 mV to achieve a current density of 100 mA cm, and they exhibit long-term stability at 1000 mA cm over 7000 h.

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Electrosynthesis of ammonia from nitrate reduction receives extensive attention recently for its relatively mild conditions and clean energy requirements, while most existed electrochemical strategies can only deliver a low yield rate and short duration for the lack of stable ion exchange membranes at high current density. Here, a bipolar membrane nitrate reduction process is proposed to achieve ionic balance, and increasing water dissociation sites is delivered by constructing a three-dimensional physically interlocked interface for the bipolar membrane. This design simultaneously boosts ionic transfer and interfacial stability compared to traditional ones, successfully reducing transmembrane voltage to 1.

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The application of membrane electrode assemblies is considered a promising approach for increasing the energy efficiency of conventional alkaline water electrolysis. However, previous investigations have mostly focused on improving membrane conductivity and electrocatalyst activity. This study reports an all-in-one membrane electrode assembly obtained by de novo design.

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The design of high-performance and durable electrodes for the oxygen evolution reaction (OER) is crucial for pure-water-fed anion exchange membrane water electrolysis (AEMWE). In this study, an integrated electrode with vertically aligned ionomer-incorporated nickel-iron layered double hydroxide nanosheet arrays, used on one side of the liquid/gas diffusion layer, is fabricated for the OER. Transport highways in the fabricated integrated electrode, significantly improve the transport of liquid/gas, hydroxide ions, and electron in the anode, resulting in a high current density of 1900 mA cm at 1.

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The effective capture of radioiodine, produced or released from nuclear-related activities, is of paramount importance for the sustainable development of nuclear energy. Here, a series of zirconium-based metal-organic frameworks (Zr-MOFs), with a Zr(μ-O)(μ-OH) cluster and various carboxylate linkers, were investigated for the capture of volatile iodine. Their adsorption kinetics and recyclability were investigated in dry and humid environments.

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