Ramírez-Soria Edgar H, García-Dalí Sergio, Munuera Jose M, Carrasco Daniel F, Villar-Rodil Silvia, Tascón Juan M D, Paredes Juan I, Bonilla-Cruz José
Advanced Functional Materials & Nanotechnology Group, Centro de Investigación en Materiales Avanzados S. C. (CIMAV-Unidad Monterrey), Av. Alianza Norte 202, Autopista Monterrey-Aeropuerto Km 10, PIIT, Apodaca, Nuevo León C.P. 66628, México.
Instituto de Ciencia y Tecnología del Carbono, INCAR-CSIC, C/Francisco Pintado Fe 26, Oviedo 33011, Spain.
ACS Appl Mater Interfaces. 2021 Nov 24;13(46):54860-54873. doi: 10.1021/acsami.1c12135. Epub 2021 Nov 9.
Phosphate-functionalized carbon-based nanomaterials have attracted significant attention in recent years owing to their outstanding behavior in electrochemical energy-storage devices. In this work, we report a simple approach to obtain phosphate-functionalized graphene (PFG) via anodic exfoliation of graphite at room temperature with a high yield. The graphene nanosheets were obtained via anodic exfoliation of graphite foil using aqueous solutions of HPO or NaPO in the dual role of phosphate sources and electrolytes, and the underlying exfoliation/functionalization mechanisms are proposed. The effect of electrolyte concentration was studied, as low concentrations do not lead to a favorable graphite exfoliation and high concentrations produce fast graphite expansion but poor layer-by-layer delamination. The optimal concentrations are 0.25 M HPO and 0.05 M NaPO, which also exhibited the highest phosphorus contents of 2.2 and 1.4 at. %, respectively. Furthermore, when PFG-acid at 0.25 M and PFG-salt at 0.05 M were tested as an electrode material for capacitive energy storage in a three-electrode cell, they achieved a competitive performance of ∼375 F/g (540 F/cm) and 356 F/g (500 F/cm), respectively. Finally, devices made up of symmetric electrode cells obtained using PFG-acid at 0.25 M possess energy and power densities up to 17.6 Wh·kg (25.3 Wh·L) and 10,200 W/kg; meanwhile, PFG-salt at 0.05 M achieved values of 14.9 Wh·kg (21.3 Wh·L) and 9400 W/kg, with 98 and 99% of capacitance retention after 10,000 cycles, respectively. The methodology proposed here also promotes a circular-synthesis process to successfully achieve a more sustainable and greener energy-storage device.
近年来,磷酸官能化的碳基纳米材料因其在电化学储能器件中的优异性能而备受关注。在这项工作中,我们报告了一种通过室温下石墨的阳极剥离以高产率获得磷酸官能化石墨烯(PFG)的简单方法。石墨烯纳米片是通过使用HPO或NaPO水溶液对石墨箔进行阳极剥离而获得的,HPO或NaPO在其中兼具磷酸盐源和电解质的双重作用,并提出了潜在的剥离/官能化机制。研究了电解质浓度的影响,因为低浓度不会导致有利的石墨剥离,而高浓度会使石墨快速膨胀,但层间分层效果不佳。最佳浓度分别为0.25 M HPO和0.05 M NaPO,它们的磷含量也分别最高,为2.2 at.%和1.4 at.%。此外,当测试0.25 M的PFG-酸和0.05 M的PFG-盐作为三电极电池中电容储能的电极材料时,它们分别实现了约375 F/g(540 F/cm³)和356 F/g(500 F/cm³)的竞争性能。最后,由0.25 M的PFG-酸制成的对称电极电池组成的器件,其能量密度和功率密度分别高达17.6 Wh·kg⁻¹(25.3 Wh·L⁻¹)和10200 W/kg;同时,0.05 M的PFG-盐的能量密度和功率密度分别为14.9 Wh·kg⁻¹(21.3 Wh·L⁻¹)和9400 W/kg,在10000次循环后电容保持率分别为98%和99%。这里提出的方法还推动了循环合成过程,以成功实现更可持续、更环保的储能器件。