Synthesis and characterization of nitrogen-doped graphene hydrogels by hydrothermal route with urea as reducing-doping agents

石墨烯 材料科学 热重分析 拉曼光谱 X射线光电子能谱 介孔材料 氧化物 氮气 化学工程 核化学 纳米技术 化学 有机化学 催化作用 物理 工程类 光学 冶金
作者
Hui-Lin Guo,Peng Su,Xiaofeng Kang,Ning Sheng-ke
出处
期刊:Journal of materials chemistry. A, Materials for energy and sustainability [Royal Society of Chemistry]
卷期号:1 (6): 2248-2255 被引量:369
标识
DOI:10.1039/c2ta00887d
摘要

Nitrogen-doped graphene hydrogels (NGHs) were synthesized through a one-pot hydrothermal route with graphene oxide (GO) as raw material and urea as reducing-doping agents. The morphology, structure, and components of the NGHs were characterized by scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, methylene blue adsorption, thermogravimetric analysis and electrical conductivity measurements. The results demonstrated that nitrogen was doped into the graphene plane at the same time as the GO sheets were reduced, and the nitrogen content incorporated into the graphene lattice was in the range of 3.95 to 6.61 at.% with pyrrolic N as the main component. The NGHs contained about 97.6 wt% water and have a large specific surface area (SSA) of >1300 m2 g−1 in the wet state. In addition, the electrochemical performance of the NGHs was investigated. The sample NGHs-4 with a nitrogen content of 5.86 at.% and SSA of 1521 ± 60 m2 g−1 in the wet state showed excellent capacitive behavior (308 F g−1 at 3 A g−1) and superior cycling stability (92% retention after 1200 cycles) in 6 mol L−1 KOH. The experimental results indicated that not only the N-content but also the N-type have very significant impact on the capacitive behavior. Furthermore, NGHs strongly influenced the electrochemical properties because of their high SSAs and mesoporous structure.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
爱听歌的孤容完成签到 ,获得积分10
1秒前
慕青应助想人陪的向南采纳,获得10
1秒前
安白发布了新的文献求助10
2秒前
2秒前
3秒前
fagfagsf发布了新的文献求助10
9秒前
tttttt完成签到,获得积分10
11秒前
上善若水完成签到 ,获得积分10
13秒前
13秒前
达瓦里希完成签到 ,获得积分10
18秒前
18秒前
谷德耐给谷德耐的求助进行了留言
21秒前
Hello应助Yunus采纳,获得10
22秒前
orixero应助lv采纳,获得10
23秒前
田様应助聪明的冬瓜采纳,获得10
23秒前
bxll完成签到 ,获得积分10
26秒前
wy.he应助黑米粥采纳,获得10
27秒前
wy.he应助黑米粥采纳,获得10
28秒前
ding应助黑米粥采纳,获得10
28秒前
爆米花应助黑米粥采纳,获得10
28秒前
想人陪的向南完成签到,获得积分10
29秒前
30秒前
自信夜春完成签到,获得积分10
31秒前
奋斗机器猫完成签到 ,获得积分10
34秒前
35秒前
cxwcn发布了新的文献求助10
35秒前
35秒前
共享精神应助假面绅士采纳,获得10
40秒前
Yunus发布了新的文献求助10
41秒前
研友_VZG7GZ应助自由采纳,获得10
41秒前
jiujiuwo完成签到,获得积分10
42秒前
CipherSage应助ykxa采纳,获得10
42秒前
42秒前
47秒前
L_online完成签到 ,获得积分10
47秒前
啵啵冰应助清晨采纳,获得50
48秒前
50秒前
学术完成签到 ,获得积分10
53秒前
54秒前
54秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Mixing the elements of mass customisation 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3777922
求助须知:如何正确求助?哪些是违规求助? 3323546
关于积分的说明 10214842
捐赠科研通 3038738
什么是DOI,文献DOI怎么找? 1667634
邀请新用户注册赠送积分活动 798236
科研通“疑难数据库(出版商)”最低求助积分说明 758315