Patterson Nigel, Xiao Bo, Ignaszak Anna
Department of Chemistry, University of New Brunswick 30 Dineen Drive (Toole Hall) Fredericton NB Canada
School of Chemistry and Chemical Engineering, Queen's University Belfast Stranmillis Road (David Kier Building) Belfast BT9 5AG UK.
RSC Adv. 2020 May 27;10(34):20162-20172. doi: 10.1039/d0ra02154g. eCollection 2020 May 26.
Due to their large specific surface areas and porosity, metal-organic frameworks (MOFs) have found many applications in catalysis, gas separation, and gas storage. However, their use as electronic components such as supercapacitors is stunted due to their poor electrical conductivity. We report a remedy for this by combining the MOF structure with polypyrrole (PPy), a well-known conductive polymer. Three MOFs are studied for modification to this end: CPO-27-Ni and CPO-27-Co (MDOBDC, M = Ni, Co, DOBDC = 2,5-dihydroxy-1,4-benzenedicarboxylate) and HKUST-1 (Cu(BTC), BTC = 1,3,5 benzenetricarboxylate). The gravimetric capacitance of pure MOFs is boosted several orders of magnitude after reinforcement of PPy (, from 0.679 to 185 F g for HKUST-1 and PPy-HKUST-1, respectively), and is much higher than reported for pure PPy. In total, these PPy--MOFs exhibit specific capacitances up to 354 F g, retaining 70% of this value even after 2500 cycles. Among them, the highest capacitance is found for PPy-CPO-27-Ni (354 F g), followed by PPy-CPO-27-Co (263 F g) and PPy-HKUST-1 (185 F g). The maximum operating potential for these electrodes is 0.5 V, which is restricted by the contact of MOF with aqueous electrolyte and with extremely low PPy content. As a solution, higher PPy loading and rational adjustment of particle size and porosity of both MOF and PPy are recommended so that the MOF/electrolyte interface is limited, leading to more robust electrode. The work completed here describes a highly promising approach to tackling the electrically insulating nature of MOFs, paving the way for their use in electrochemical energy storage devices.
由于金属有机框架材料(MOFs)具有较大的比表面积和孔隙率,它们在催化、气体分离和气体储存等领域有许多应用。然而,由于其导电性较差,它们作为超级电容器等电子元件的应用受到了限制。我们通过将MOF结构与聚吡咯(PPy)(一种著名的导电聚合物)相结合,报道了一种解决方法。为此研究了三种用于改性的MOF:CPO - 27 - Ni和CPO - 27 - Co(MDOBDC,M = Ni、Co,DOBDC = 2,5 - 二羟基 - 1,4 - 苯二甲酸)以及HKUST - 1(Cu(BTC),BTC = 1,3,5 - 苯三甲酸)。在PPy增强后,纯MOF的重量电容提高了几个数量级(例如,HKUST - 1和PPy - HKUST - 1的重量电容分别从0.679 F/g提高到185 F/g),并且远高于报道的纯PPy的电容。总的来说,这些PPy - MOF表现出高达354 F/g的比电容,即使在2500次循环后仍保留该值的70%。其中,PPy - CPO - 27 - Ni的电容最高(354 F/g),其次是PPy - CPO - 27 - Co(263 F/g)和PPy - HKUST - 1(185 F/g)。这些电极的最大工作电位为0.5 V,这受到MOF与水性电解质接触以及PPy含量极低的限制。作为一种解决方案,建议提高PPy负载量,并合理调整MOF和PPy的粒径和孔隙率,以使MOF/电解质界面受到限制,从而得到更坚固的电极。这里完成的工作描述了一种极具前景的方法来解决MOF的电绝缘性质,为其在电化学储能装置中的应用铺平了道路。