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Constructing Conductive Interfaces between Nickel Oxide Nanocrystals and Polymer Carbon Nitride for Efficient Electrocatalytic Oxygen Evolution Reaction

机译:在氧化镍纳米晶体和聚合物氮化碳之间构建导电界面,以进行高效的电催化氧释放反应

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摘要

Combining transition metal oxide catalysts with conductive carbonaceous material is a feasible way to improve the conductivity. However, the electrocatalytic performance is usually not distinctly improved because the interfacial resistance between metal oxides and carbon is still large and thereby hinders the charge transport in catalysis. Herein, the conductive interface between poorly conductive NiO nanoparticles and semi-conductive carbon nitride (CN) is constructed. The NiO/CN exhibits much-enhanced oxygen evolution reaction (OER) performance than corresponding NiO and CN in electrolytes of KOH solution and phosphate buffer saline, which is also remarkably superior over NiO/C, commercial RuO2, and mostly reported NiO-based catalysts. X-ray photoelectron spectroscopy and extended X-ray absorption fine structure spectrum reveal that a metallic Ni-N bond is formed between NiO and CN. Density functional theory calculations suggest that NiO and CN linked by a Ni-N bond possess a low Gibbs energy for OER intermediate adsorptions, which not only improves the transfer of charge but also promotes the transmission of mass in OER. The metal-nitrogen bonded conductive and highly active interface pervasively exists between CN and other transition metal oxides including Co3O4, CuO, and Fe2O3, making it promising as an inexpensive catalyst for efficient water splitting.
机译:将过渡金属氧化物催化剂与导电碳质材料结合使用是提高电导率的可行方法。但是,由于金属氧化物和碳之间的界面电阻仍然很大,因此阻碍了催化中的电荷迁移,因此通常不能明显改善电催化性能。在此,构造了导电性差的NiO纳米颗粒和半导体性的氮化碳(CN)之间的导电界面。 NiO / CN在KOH溶液和磷酸盐缓冲盐水的电解质中比相应的NiO和CN表现出更大的氧释放反应(OER)性能,这也明显优于NiO / C,市售RuO2和大多数报道的基于NiO的催化剂。 X射线光电子能谱和扩展的X射线吸收精细结构光谱表明,NiO和CN之间形成金属Ni-N键。密度泛函理论计算表明,通过Ni-N键连接的NiO和CN在OER中间吸附方面具有较低的吉布斯能量,这不仅改善了电荷转移,还促进了OER中质量的传递。 CN与其他过渡金属氧化物(包括Co3O4,CuO和Fe2O3)之间普遍存在金属-氮键键合的导电性和高活性界面,使其有望成为廉价的高效水分解催化剂。

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