BCN nanosheets templated by g-C3N4 for high performance capacitive deionization
Capacitive deionization (CDI) is an emerging technology for removing charged ions from saline water and has attracted much attention in recent years. Developing a new electrode material with a reasonable structure is of great significance for obtaining high CDI performance. Herein, two-dimensional (...
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Published in | Journal of materials chemistry. A, Materials for energy and sustainability Vol. 6; no. 30; pp. 14644 - 14650 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cambridge
Royal Society of Chemistry
2018
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Subjects | |
Online Access | Get full text |
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Summary: | Capacitive deionization (CDI) is an emerging technology for removing charged ions from saline water and has attracted much attention in recent years. Developing a new electrode material with a reasonable structure is of great significance for obtaining high CDI performance. Herein, two-dimensional (2D) boron carbon nitride (BCN) nanosheets were fabricated using a new approach, which uses g-C3N4 as both the template and the nitrogen source, boric acid as the boron source and a subsequent pyrolysis process. The as-prepared BCN nanosheets show a pore structure with a high specific surface area and were investigated as CDI electrode materials for the first time. Moreover, the high heteroatom content, with a potential synergistic effect of N and B atoms, results in fast ion diffusion and good charge transfer ability. The BCN nanosheets demonstrate a high salt adsorption capacity of 13.6 mg g−1 at 1.4 V applied voltage when the initial NaCl concentration is 500 mg L−1. The BCN electrodes also exhibited better cyclic stability over 15 adsorption–desorption cycles. These results indicate that BCN nanosheets should be practicable candidates for high performance CDI electrode materials. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2050-7488 2050-7496 2050-7496 |
DOI: | 10.1039/c8ta04058c |