Li Juntao, Gadipelli Srinivas
Department of Chemistry, University College London, London, WC1H 0AJ, UK.
Department of Chemical Engineering, University College London, London, WC1E 7JE, UK.
Chemistry. 2020 Nov 6;26(62):14167-14172. doi: 10.1002/chem.202002702. Epub 2020 Sep 30.
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.
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。