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用于析氧反应的沸石咪唑酯骨架材料的合成与优化

Synthesis and Optimization of Zeolitic Imidazolate Frameworks for the Oxygen Evolution Reaction.

作者信息

Li Juntao, Gadipelli Srinivas

机构信息

Department of Chemistry, University College London, London, WC1H 0AJ, UK.

Department of Chemical Engineering, University College London, London, WC1E 7JE, UK.

出版信息

Chemistry. 2020 Nov 6;26(62):14167-14172. doi: 10.1002/chem.202002702. Epub 2020 Sep 30.

Abstract

Metal-organic frameworks/zeolitic imidazolate frameworks (MOFs/ZIFs) and their post-synthesis modified nanostructures, such as oxides, hydroxides, and carbons have generated significant interest for electrocatalytic reactions. In this work, a high and durable oxygen evolution reaction (OER) performance directly from bimetallic Zn Co -ZIF samples is reported, without carrying out high-temperature calcination and/or carbonization. ZIFs can be reproducibly and readily synthesized in large scale at ambient conditions. The bimetallic ZIFs show a systematic and gradually improved OER activity with increasing cobalt concentration. A further increase in OER activity is evidenced in ZIF-67 polyhedrons with controlled particle size of <200 nm among samples of different sizes between 50 nm and 2 μm. Building on this, a significantly enhanced, >50 %, OER activity is obtained with ZIF-67/carbon black, which shows a low overpotential of approximately 320 mV in 1.0 m KOH electrolyte. Such activity is comparable to or better than numerous MOF/ZIF-derived electrocatalysts. The optimized ZIF-67 sample also exhibits increased activity and durability over 24 h, which is attributed to an in situ developed active cobalt oxide/oxyhydroxide related nanophase.

摘要

金属有机框架材料/沸石咪唑酯骨架材料(MOF/ZIF)及其合成后修饰的纳米结构,如氧化物、氢氧化物和碳,已在电催化反应中引起了广泛关注。在这项工作中,报道了双金属Zn-Co-ZIF样品在不进行高温煅烧和/或碳化的情况下,直接具有高且持久的析氧反应(OER)性能。ZIF能够在环境条件下可重复且容易地大规模合成。随着钴浓度的增加,双金属ZIF表现出系统且逐渐提高的OER活性。在50 nm至2 μm之间不同尺寸的样品中,粒径控制在<200 nm的ZIF-67多面体的OER活性有进一步提高。在此基础上,ZIF-67/炭黑的OER活性显著增强,提高了>50%,在1.0 m KOH电解液中显示出约320 mV的低过电位。这种活性与许多MOF/ZIF衍生的电催化剂相当或更好。优化后的ZIF-67样品在24小时内也表现出活性和耐久性的提高,这归因于原位形成的与活性氧化钴/羟基氧化钴相关的纳米相。

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