• 文献标题:   High Performance Na-O-2 Batteries and Printed Microsupercapacitors Based on Water-Processable, Biomolecule-Assisted Anodic Graphene
  • 文献类型:   Article
  • 作  者:   MUNUERA JM, PAREDES JI, ENTERRIA M, VILLARRODIL S, KELLY AG, NALAWADE Y, COLEMAN JN, ROJO T, ORTIZVITORIANO N, MARTINEZALONSO A, TASCON JMD
  • 作者关键词:   graphene, electrochemical exfoliation, biomolecule, metaloxygen batterie, microsupercapacitor
  • 出版物名称:   ACS APPLIED MATERIALS INTERFACES
  • ISSN:   1944-8244 EI 1944-8252
  • 通讯作者地址:   CSIC
  • 被引频次:   3
  • DOI:   10.1021/acsami.9b15509
  • 出版年:   2020

▎ 摘  要

Integrated approaches that expedite the production and processing of graphene into useful structures and devices, particularly through simple and environmentally friendly strategies, are highly desirable in the efforts to implement this two-dimensional material in state-of-the-art electrochemical energy storage technologies. Here, we introduce natural nucleotides (e.g., adenosine monophosphate) as bifunctional agents for the electrochemical exfoliation and dispersion of graphene nanosheets in water. Acting both as exfoliating electrolytes and colloidal stabilizers, these biomolecules facilitated access to aqueous graphene bio-inks that could be readily processed into aerogels and inkjet-printed interdigitated patterns. Na-O-2 batteries assembled with the graphene-derived aerogels as the cathode and a glyme-based electrolyte exhibited a full discharge capacity of similar to 3.8 mAh cm(-2) at a current density of 0.2 mA cm(-2). Moreover, shallow cycling experiments (0.5 mAh cm(-2)) boasted a capacity retention of 94% after 50 cycles, which outperformed the cycle life of prior graphene-based cathodes for this type of battery. The positive effect of the nucleotide-adsorbed nanosheets on the battery performance is discussed and related to the presence of the phosphate group in these biomolecules. Microsupercapacitors made from the interdigitated graphene patterns as the electrodes also displayed a competitive performance, affording areal and volumetric energy densities of 0.03 mu Wh cm(-2) and 1.2 mWh cm(-3) at power densities of 0.003 mW cm(-2) and 0.1 W cm(-3), respectively. Taken together, by offering a green and straightforward route to different types of functional graphene-based materials, the present results are expected to ease the development of novel energy storage technologies that exploit the attractions of graphene.