4.6 Article

Protonation of Graphitic Carbon Nitride (g-C3N4) for an Electrostatically Self-Assembling Carbon@g-C3N4 Core Shell Nanostructure toward High Hydrogen Evolution

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 5, Issue 8, Pages 7093-7103

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.7b01312

Keywords

Polymeric carbon nitride; Electrostatic self-assembly; Metal-free core-shell nanostructure; Broadened light absorption; Hydrogen evolution

Funding

  1. National Natural Science Foundation [51672220]
  2. 111 Program of MOE [B08040]
  3. National Defense Science Foundation [32102060303]
  4. Fundamental Research Funds for the Central Universities [3102014JGY01004]
  5. Xi'an Science and Technology Foundation
  6. Shaanxi Provincial Science Foundation
  7. NPU Gaofeng Project of China

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The development of new, appealing metal-free photo catalysts is of great significance for photocatalytic hydrogen evolution. Herein, an electrostatic self-assembly method to form a unique core shell architecture of a colloid of carbon spheres with graphitic carbon nitride (g-C3N4) has been developed by a one-step chemical solution route. The chemical protonation of g-C3N4 solids with strong oxidizing acids (such as HNO3) is an efficient pathway toward the sol procedure of stable carbon nitride colloids, which can cover the surface of carbon spheres via electrostatic adsorption. On account of the unique polymeric matrix of g-C3N4 and reversible hydrogen bonding, the carbon@g-C3N4 derived from the sol solution showed high mechanical stability with broadened light absorption and enhanced conductivity for charge transport. Thus, the carbon@g-C3N4 core shell structure exhibited remarkably enhanced photoelectrochemical performance. This polymer system is envisaged to hybridize with desirable functionalities (such as carbon nanorods) to form unique architectures for various applications.

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