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用于高效析氧反应的自支撑超薄二维金属有机框架纳米片电极的配体辅助可控生长

Ligand-Assisted Controllable Growth of Self-Supporting Ultrathin Two-Dimensional Metal-Organic Framework Nanosheet Electrodes for an Efficient Oxygen Evolution Reaction.

作者信息

Wang Lei, Wang Ani, Fan WenXia, Pan Jie, Xue Zhenzhen, Wang Guoming

机构信息

College of Chemistry and Chemical Engineering, Qingdao University, Qingdao, Shandong 266071, P. R. China.

出版信息

Inorg Chem. 2022 Sep 19;61(37):14899-14907. doi: 10.1021/acs.inorgchem.2c02669. Epub 2022 Sep 2.

DOI:10.1021/acs.inorgchem.2c02669
PMID:36052825
Abstract

Rational design of metal-organic frameworks (MOFs) into ultrathin two-dimensional (2D) nanosheets with controllable thickness is significantly attractive but is also a significant challenge. Herein, the authors report, for the first time, the synthesis of ultrathin 2D nickel-based MOF nanosheets with a thickness of only about 2 nm via a ligand-assisted controllable growth strategy, which cannot be acquired from the exfoliation of their bulky counterparts or the conventional hydrothermal method. The correlation between 2D nanosheets and crystal growth preference was demonstrated through a judicious choice of a specific [Ni(BIP)(-BDC)(HO)] framework (BIP = (3,5-bis(1-imidazoly)pyridine), -HBDC = terephthalic acid) to underlie the geometry of the resultant morphology. Under the modulation by the dosage of terephthalic acid through a corrosion-dissolution-coordination process, the nanosheets of Ni-MOFs with a controllable thickness can be tuned to 50 and 100 nm. Ultrathin 2D Ni-MOF nanosheet-derived N-doped Ni@carbon exhibits a satisfactory electrocatalytic performance with a small overpotential of 170 mV to achieve a current density of 10 mA cm, much outperforming the bulk Ni-MOF and the most reported non-noble-metal oxygen evolution reaction electrocatalysts to date. It is believed that this ligand-assisted controllable growth strategy represents a novel and simple path to prepare high-performance MOF-based electrocatalysts for wide applications.

摘要

将金属有机框架(MOFs)合理设计成具有可控厚度的超薄二维(2D)纳米片极具吸引力,但也是一项重大挑战。在此,作者首次报道了通过配体辅助可控生长策略合成厚度仅约2 nm的超薄二维镍基金属有机框架纳米片,这无法通过其块状对应物的剥离或传统水热法获得。通过明智地选择特定的[Ni(BIP)(-BDC)(HO)]框架(BIP = (3,5-双(1-咪唑基)吡啶),-HBDC = 对苯二甲酸)来证明二维纳米片与晶体生长偏好之间的相关性,以支撑所得形态的几何结构。通过对苯二甲酸用量的调制,经过腐蚀-溶解-配位过程,可将厚度可控的镍基金属有机框架纳米片调整为50和100 nm。超薄二维镍基金属有机框架纳米片衍生的氮掺杂镍@碳表现出令人满意的电催化性能,在电流密度为10 mA cm时过电位仅为170 mV,大大优于块状镍基金属有机框架和迄今为止报道的大多数非贵金属析氧反应电催化剂。据信,这种配体辅助可控生长策略代表了一种新颖且简单的途径,可用于制备广泛应用的高性能基于金属有机框架的电催化剂。

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