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Activation of Carbon Nitride Solids by Protonation: Morphology Changes, Enhanced Ionic Conductivity, and Photoconduction Experiments

Zhang, Yuanjian, Thomas, Arne, Antonietti, Markus, Wang, Xinchen·2009·Journal of the American Chemical Society

Abstract

Covalently bonded carbon nitride materials (e.g., g-C(3)N(4)) have numerous potential applications ranging from semiconductors to fuel cells. But their solubility is poor, which makes characterization and processing difficult. Moreover, the chemistry of the as-synthesized carbon nitrides has been widely neglected. Here we report that some of these handicaps might be overcome by a controllable and reversible protonation. It was found that protonation not only provides better dispersion and exposes a high surface area for g-C(3)N(4) but also enables an adjustment of electronic band gaps and higher ionic conductivity. Recovery or deprotonation toward the original g-C(3)N(4) could be obtained by simple heating, which enables improved sintering but also a potential preservation of the higher surface area of the protonated material. This proton-enhanced sintering process allowed for the first time direct measurement of the photoconductivity of the material. By aid of protonation, other promising g-C(3)N(4) based hybrid composites could also be facilely obtained by simple counteranion exchange.

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Metadata

Authors
Zhang, Y., Thomas, A., Antonietti, M., & Wang, X.
Venue
Journal of the American Chemical Society
Published
2008-12-10
Volume
131
Issue
1
Pages
50-51
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1987444508
Cited by
801
References
0
FWCI
3.96
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Activation of Carbon Nitride Solids by Protonation: Morphology Changes, Enhanced Ionic Conductivity, and Photoconduction Experiments. https://app.cochat.ai/papers/10.1021/ja808329f
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Zhang, Y., Thomas, A., Antonietti, M., & Wang, X. (2009). Activation of Carbon Nitride Solids by Protonation: Morphology Changes, Enhanced Ionic Conductivity, and Photoconduction Experiments. Journal of the American Chemical Society. https://doi.org/10.1021/ja808329f

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