Nitrogen-doped carbon materials produced from hydrothermally treated tannin

被引:125
作者
Braghiroli, F. L. [1 ,2 ]
Fierro, V. [1 ]
Izquierdo, M. T. [3 ]
Parmentier, J. [4 ]
Pizzi, A. [5 ]
Celzard, A. [1 ,2 ]
机构
[1] ENSTIB, Inst Jean Lamour, UMR 7198, CNRS, F-88051 Epinal 9, France
[2] Univ Lorraine, ENSTIB, F-88051 Epinal 9, France
[3] CSIC, ICB, Inst Carboquim, Zaragoza 50018, Spain
[4] Univ Haute Alsace, CNRS, LRC 7228, Inst Sci Mat Mulhouse, F-68057 Mulhouse, France
[5] Univ Lorraine, ENSTIB, LERMAB, F-88051 Epinal 9, France
关键词
OXYGEN-REDUCTION; ACTIVATED CARBON; ELECTROCHEMICAL PERFORMANCE; POLYFLAVONOID TANNINS; AQUEOUS-SOLUTIONS; ONE-STEP; ADSORPTION; PRECURSORS; CARBONIZATION; GRAPHENE;
D O I
10.1016/j.carbon.2012.07.027
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This manuscript presents a simple one-pot synthesis for producing nitrogen-doped carbon materials (NCMs) with nitrogen content up to 6.3 wt.%. Carbon gels were produced by direct pyrolysis without the expensive step of supercritical drying in CO2. NCMs were synthesized by hydrothermal carbonization (HTC) of aminated tannin. Amination of tannin was carried out in aqueous ammonia solution according to two different methods: (1) amination at room temperature followed by evaporation and HTC of the resultant powder in pure water at 180 degrees C for 24 h, or (2) direct HTC in the same conditions of the tannin-ammonia solution. In both cases, further pyrolysis was carried out at 900 degrees C under nitrogen flow. We obtained very different NCMs depending on the method. Method (1) led to microporous carbon gels having a surface area of 500 M(2)g(-1) without need of supercritical drying, and a nitrogen content of 2.9 wt.%, whereas method (2) led to carbons microspheres arranged in pearl-necklace structure, having a surface area around 60 m(2)g(-1) and a higher nitrogen content of 6.3 wt.%. In both cases, X-ray photoelectron spectroscopy showed mainly pyrrolic and pyridinic nitrogen functionalities. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5411 / 5420
页数:10
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