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高熵催化剂驱动的 N 电解电池:从理论预测到原型模型。

Battery-Driven N Electrolysis Enabled by High-Entropy Catalysts: From Theoretical Prediction to Prototype Model.

机构信息

Key Laboratory for Soft Chemistry and Functional Materials, School of Chemistry and Chemical Engineering, School of Energy and Power Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.

出版信息

Small. 2022 Mar;18(11):e2106358. doi: 10.1002/smll.202106358. Epub 2022 Jan 9.

Abstract

A small-scale standalone device of nitrogen (N ) splitting holds great promise for producing ammonia (NH ) in a decentralized manner as the compensation or replacement of centralized Haber-Bosch process. However, the design of such a device has been impeded by sluggish kinetics of its half reactions, i.e., cathodic N reduction reaction (NRR) and anodic oxygen evolution reaction (OER). Here, it is predicted from density function theory that high-entropy oxides (HEOs) are potential catalysts for promoting NRR and OER, and subsequently develop a facile procedure to synthesize HEOs in the morphology of sea urchin-shaped hollow nanospheres assembled from ultrathin nanosheets. The excellent electrocatalytic activities of HEOs for both NRR (NH yield rate: 47.58 µg h mg and Faradaic efficiency (FE): 10.74%) and OER (215 mV @10 mA cm ) are demonstrated. Consequently, a prototype device of N electrolysis driven by commercial batteries is constructed, which can operate smoothly and deliver remarkable NH yield rate (41.11 µg h mg ) and FE (14.14%). Further mechanism study has attributed the excellent catalytic performances of HEOs to their unique electronic structures originated from multi-metal synergistic effects and entropy increase effects. The work will provide new clues for designing versatile catalysts and devices for large-scale industrialization.

摘要

一种小规模的独立氮 (N) 分离装置有望以分散的方式生产氨 (NH),作为对集中 Haber-Bosch 工艺的补偿或替代。然而,由于其半反应(即阴极 N 还原反应 (NRR) 和阳极氧析出反应 (OER))的动力学缓慢,这种装置的设计受到了阻碍。在这里,通过密度泛函理论预测,高熵氧化物 (HEO) 是促进 NRR 和 OER 的潜在催化剂,并随后开发了一种简便的方法来合成海胆状空心纳米球的形态的 HEO,这些纳米球由超薄纳米片组装而成。HEO 对 NRR(NH 产率:47.58 µg h mg 和法拉第效率 (FE):10.74%)和 OER(215 mV @10 mA cm )都表现出优异的电催化活性。因此,构建了由商用电池驱动的 N 电解原型装置,该装置可以平稳运行,并提供显著的 NH 产率(41.11 µg h mg)和 FE(14.14%)。进一步的机制研究将 HEO 的优异催化性能归因于它们独特的电子结构,这源于多金属协同效应和熵增加效应。这项工作将为设计用于大规模工业化的多功能催化剂和装置提供新的线索。

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