Doping of graphitic carbon nitride for photocatalysis: A review

石墨氮化碳 光催化 非金属 兴奋剂 载流子 异质结 材料科学 氮化碳 带隙 可见光谱 催化作用 纳米技术 金属 光电子学 化学 有机化学 冶金
作者
Longbo Jiang,Xingzhong Yuan,Yang Pan,Jie Liang,Guangming Zeng,Zhibin Wu,Hou Wang
出处
期刊:Applied Catalysis B-environmental [Elsevier BV]
卷期号:217: 388-406 被引量:1572
标识
DOI:10.1016/j.apcatb.2017.06.003
摘要

As a fascinating conjugated polymer, graphitic carbon nitride (g-C3N4) has been the hotspot in the materials science as a metal-free and visible-light-responsive photocatalyst. Pure g-C3N4 suffers from the insufficient sunlight absorption, low surface area and the fast recombination of photo-induced electron-hole pairs, resulting in low photocatalytic activity. Element doping is known to be an efficient method to tune the unique electronic structure and band gap of g-C3N4, which considerably broaden the light responsive range and enhance the charge separation. This review summarizes the recent progress in the development of efficient and low cost doped g-C3N4 systems in various realms such as photocatalytic hydrogen evolution, reduction of carbon dioxide, photocatalytic removal of contaminants in wastewater and gas phase. Typically, metal doping, nonmetal doping, co-doping and heterojunction based on doped g-C3N4 have been explored to simultaneously tune the crystallographic, textural and electronic structures for improving photocatalytic activity by enhancing the light absorption, facilitating the charge separation and transportation and prolonging the charge carrier lifetime. Finally, the current challenges and the crucial issues of element doped g-C3N4 photocatalysts that need to be addressed in future research are presented. This review presented herein can pave a novel avenue and add invaluable knowledge to the family of element doped g-C3N4 for the develop of more effective visible-light-driven photocatalysts.
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
上官若男应助来LAIhuhu采纳,获得10
1秒前
曾经翩跹发布了新的文献求助30
2秒前
happiness完成签到 ,获得积分10
3秒前
w1完成签到 ,获得积分10
5秒前
学pde的小丸子完成签到,获得积分10
5秒前
今后应助青青采纳,获得10
6秒前
fu发布了新的文献求助10
7秒前
斯文败类应助无私匕采纳,获得10
7秒前
踏实之柔完成签到,获得积分10
7秒前
科研通AI6.4应助wangli采纳,获得10
8秒前
76ers完成签到,获得积分10
10秒前
美好胡萝卜完成签到,获得积分20
12秒前
12秒前
12秒前
森火完成签到 ,获得积分10
12秒前
13秒前
脑洞疼应助虞丹萱采纳,获得10
14秒前
zsp完成签到 ,获得积分10
15秒前
潘岩完成签到,获得积分20
15秒前
ThomsonLi6完成签到,获得积分10
15秒前
16秒前
彭于晏应助美好胡萝卜采纳,获得10
16秒前
duanxihang完成签到,获得积分20
17秒前
17秒前
huanhuan发布了新的文献求助10
17秒前
陈平安发布了新的文献求助10
17秒前
18秒前
wang发布了新的文献求助10
18秒前
大个应助潘岩采纳,获得10
18秒前
19秒前
19秒前
桐桐应助科研通管家采纳,获得10
20秒前
南风知我意完成签到,获得积分0
20秒前
今后应助科研通管家采纳,获得10
20秒前
20秒前
NN应助科研通管家采纳,获得10
20秒前
chenc应助congcong采纳,获得10
20秒前
爆米花应助科研通管家采纳,获得10
20秒前
CodeCraft应助科研通管家采纳,获得10
21秒前
天天快乐应助HYC采纳,获得10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7746051
求助须知:如何正确求助?哪些是违规求助? 9293922
关于积分的说明 20222838
捐赠科研通 7325769
什么是DOI,文献DOI怎么找? 3308041
关于科研通互助平台的介绍 2460005
邀请新用户注册赠送积分活动 2319514