A three-dimensional graphitic carbon nitride belt network for enhanced visible light photocatalytic hydrogen evolution. Issue 48 (24th November 2016)

• Record Type: Journal Article
• Authors: Zeng, Yunxiong; Liu, Chengbin; Wang, Longlu; Zhang, Shuqu; Ding, Yangbin; Xu, Yuzi; Liu, Yutang; Luo, Shenglian
• Is Part Of: Journal of materials chemistry. Volume 4:Issue 48(2016)
• Page Start: 19003
• Page End: 19010
• Publication Date: 2016-11-24
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c6ta07397b
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Three-dimensional (3D) network-like graphitic carbon nitride nanobelts (g-C3 N4 NBs) were facilely achieved by the hydrothermal treatment of bulk g-C3 N4 in a medium strong oxalic acid solution (1 M, pH 0.89). Abstract : Three-dimensional (3D) network-like graphitic carbon nitride nanobelts (g-C3 N4 NBs) were facilely achieved by the hydrothermal treatment of bulk g-C3 N4 in a medium strong oxalic acid solution (1 M, pH 0.89). The positions of the conduction band (CB) and valence band (VB) were upraised from −0.90 and +1.86 eV for bulk g-C3 N4 to −0.92 and +1.92 eV for g-C3 N4 NB networks with enhanced redox ability, respectively. With an optimized Pt loading of 3%, the g-C3 N4 NB networks showed excellent visible-light photocatalytic H2 production activity (1360 μmol g −1 h −1 ), which was 10.9 times higher than that of optimized 2% Pt@bulk g-C3 N4 (124.7 μmol g −1 h −1 ) using triethanolamine as a sacrificial agent. Furthermore, Pt@g-C3 N4 NBs exhibited a considerable rate of H2 evolution of 33.3 μmol g −1 h −1, much higher than 1.79 μmol g −1 h −1 for Pt@bulk g-C3 N4 in distilled water without any sacrificial agents, revealing a great potential for photocatalytic overall water splitting. This outstanding performance not only originates from its unique 3D nanostructure and prolonged electron lifetime, but also from the electronic structure modulation and improved redox capacities of the CB and VB. The pH effect of hydrothermal conditions on the g-C3 N4 molecular structure, chemical elements, optical properties and catalytic performance is also expounded. This study demonstrates a facile and environmentally friendly strategy to design highly efficient g-C3 N4 catalysts for potential applications in solar energy driven photocatalytic water splitting.