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

被引:677
作者
Zhang, Yuanjian [1 ]
Thomas, Arne [1 ]
Antonietti, Markus [1 ]
Wang, Xinchen [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, D-14424 Potsdam, Germany
关键词
S-TRIAZINE DERIVATIVES; CHEMICAL-SYNTHESIS; CONDENSATION; CRYSTALLINE; NANOTUBES; MELAMINE; BENZENE; BLUE;
D O I
10.1021/ja808329f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalently bonded carbon nitride materials (e.g., g-C3N4) 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-C3N4 but also enables an adjustment of electronic band gaps and higher ionic conductivity. Recovery or deprotonation toward the original g-C3N4 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-C3N4 based hybrid composites could also be facilely obtained by simple counteranion exchange.
引用
收藏
页码:50 / +
页数:4
相关论文
共 25 条
[1]   Ionothermal Synthesis of Crystalline, Condensed, Graphitic Carbon Nitride [J].
Bojdys, Michael J. ;
Mueller, Jens-Oliver ;
Antonietti, Markus ;
Thomas, Arne .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (27) :8177-8182
[2]   Growth confined by the nitrogen source: Synthesis of pure metal nitride nanoparticles in mesoporous graphitic carbon nitride [J].
Fischer, Anna ;
Antonietti, Markus ;
Thomas, Arne .
ADVANCED MATERIALS, 2007, 19 (02) :264-+
[3]   Synthesis of nitrogen-rich carbon nitride networks from an energetic molecular azide precursor [J].
Gillan, EG .
CHEMISTRY OF MATERIALS, 2000, 12 (12) :3906-3912
[4]   Chemical synthesis of mesoporous carbon nitrides using hard templates and their use as a metal-free catalyst for friedel-crafts reaction of benzene [J].
Goettmann, Frederic ;
Fischer, Anna ;
Antonietti, Markus ;
Thomas, Arne .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (27) :4467-4471
[5]   Synthesis of carbon nitride nanotubes with the C3N4 stoichiometry via a benzene-thermal process at low temperatures [J].
Guo, QX ;
Xie, Y ;
Wang, XJ ;
Zhang, SY ;
Hou, T ;
Lv, SC .
CHEMICAL COMMUNICATIONS, 2004, (01) :26-27
[6]   From triazines to heptazines: Deciphering the local structure of amorphous nitrogen-rich carbon nitride materials [J].
Holst, James R. ;
Gillan, Edward G. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (23) :7373-7379
[7]   Tri-s-triazine derivatives, part III.: Potassium melonate, K3[C6N7(NCN)3]•5H2O, and its potential use for the synthesis of graphite-like C3N4 materials [J].
Horvath-Bordon, E ;
Kroke, E ;
Svoboda, I ;
Fuess, H ;
Riedel, R .
NEW JOURNAL OF CHEMISTRY, 2005, 29 (05) :693-699
[8]   Hydrophobic bronsted acid-base ionic liquids based on PAMAM dendrimers with high proton conductivity and blue photoluminescence [J].
Huang, JF ;
Luo, HM ;
Liang, CD ;
Sun, IW ;
Baker, GA ;
Dai, S .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (37) :12784-12785
[9]  
INOUE S, 1966, MAKROMOLEKUL CHEM, V95, P236
[10]   Melem (2,5,8-triamino-tri-s-triazine), an important intermediate during condensation of melamine rings to graphitic carbon nitride:: Synthesis, structure determination by X-ray powder diffractometry, solid-state NMR, and theoretical studies [J].
Jürgens, B ;
Irran, E ;
Senker, J ;
Kroll, P ;
Müller, H ;
Schnick, W .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (34) :10288-10300