Bacterial-cellulose-derived carbonaceous electrode materials for water desalination via capacitive method: The crucial role of defect sites: The crucial role of defect sites

Yolanda Belaustegui, Fabiola Pantò, Leire Urbina, Maria Angeles Corcuera, Arantxa Eceiza, Alessandra Palella, Claudia Triolo, Saveria Santangelo

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18 Citations (Scopus)
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Abstract

Electrosorptive desalination is a very simple and appealing approach to satisfy the increasing demand for drinking water. The large-scale application of this technology calls for the development of easy-to-produce, cheap and highly performing electrode materials and for the identification and tailoring of their most influential properties, as well. Here, biosynthesised bacterial cellulose is used as a carbon precursor for the production of three-dimensional nanostructures endowed with hierarchically porous architecture and different density and type of intrinsic and hetero-atom induced lattice defects. The produced materials exhibit unprecedented desalination capacities for carbon-based electrodes. At an initial concentration of 585 mg L−1 (10 mmol L−1), they are able to remove from 55 to 79 mg g−1 of salt; as the initial concentration rises to 11.7 g L−1 (200 mmol L−1), their salt adsorption capacity reaches values ranging between 1.03 and 1.35 g g−1. The results of the thorough material characterisation by complementary techniques evidence that the relative amount of oxygenated surface functional species enhancing the electrode wettability play a crucial role at lower NaCl concentrations, whereas the availability of active non-sp2 defect sites for adsorption is mainly influential at higher salt concentrations.
Original languageEnglish
Article number114596
Pages (from-to)114596
Number of pages1
JournalDesalination
Volume492
DOIs
Publication statusPublished - 15 Oct 2020

Keywords

  • Bacterial cellulose
  • Raman spectroscopy
  • Lattice defects
  • Capacitive deionization

Project and Funding Information

  • Funding Info
  • L.U., M.A.C. and A.E. gratefully thank GIU18/216 - UPV/EHU Research Group for the financial support to their work.

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