Ionothermally synthesized S-scheme isotype heterojunction of carbon nitride with significantly enhanced photocatalytic performance for hydrogen evolution and carbon dioxide reduction

光催化 氮化碳 材料科学 异质结 聚合 碳纤维 化学工程 氮化物 量子效率 催化作用 光化学 纳米技术 光电子学 化学 复合数 聚合物 复合材料 有机化学 工程类 图层(电子)
作者
Senpei Tang,Shitao Yang,Yuanyuan Chen,Yi Yang,Zhenhui Li,Lin Zi,Ying Liu,Yingchun Wang,Zhiping Li,Zaihui Fu,Youji Li
出处
期刊:Carbon [Elsevier BV]
卷期号:201: 815-828 被引量:48
标识
DOI:10.1016/j.carbon.2022.09.071
摘要

Graphitic phase carbon nitride (CN) is a safe and green photocatalyst, but the activity of the pristine CN photocatalyst is still unsatisfactory due to the significant recombination of photogenerated charges, so it is still challenging to realize the practical application of CN for photocatalysis. Herein, we report that a mechanical mixture consisting of pre-thermally polymerized melamine (Me) and 3-amino-1,2,4-triazole (AT) can be transformed into a crystalline isotype heterojunction material (ISCNMT) by ionothermal synthesis. A series of characterizations and photocatalytic tests demonstrate that the polymerizability, porosity and photoelectric conversion efficiency of the constructed ISCNMT have been improved. The photogenerated charge pairs of the ISCNMT can migrate in S-scheme, indicating that ISCNMT retains the strongest reduction capacity and greatly improving the separation efficiency of photogenerated charge pairs. As a result, the ISCNMT exhibits outstanding performance. Its catalytic efficiency for visible light-triggered hydrogen evolution from water can reach 9.64 mmol·g−1·h−1 with an apparent quantum efficiency (AQE) of 26.23%, which is 21 or 45 times higher than that of the carbon nitride material directly polymerized by Me or AT (CNM or CNT). In addition, the ISCNMT has a catalytic efficiency of 15.64 μmol·g−1·h−1 for photocatalysis CO2 reduction under water vapor. This work provides a facile pathway for designing S-scheme isotype heterojunction CN-based photocatalysts for the efficient conversion of solar energy.
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
传奇3应助科研通管家采纳,获得10
刚刚
刚刚
深情安青应助科研通管家采纳,获得10
1秒前
SciGPT应助mark采纳,获得10
1秒前
完美世界应助科研通管家采纳,获得30
1秒前
星辰大海应助科研通管家采纳,获得10
1秒前
1秒前
英姑应助科研通管家采纳,获得10
1秒前
华仔应助科研通管家采纳,获得10
1秒前
掏粪男孩发布了新的文献求助10
1秒前
子木应助科研通管家采纳,获得10
2秒前
lumi应助科研通管家采纳,获得10
2秒前
Nole应助科研通管家采纳,获得10
2秒前
2秒前
香蕉觅云应助科研通管家采纳,获得10
2秒前
共享精神应助科研通管家采纳,获得10
2秒前
ansteel应助科研通管家采纳,获得10
2秒前
2秒前
过氧化氢应助科研通管家采纳,获得10
3秒前
东方元语应助科研通管家采纳,获得20
3秒前
早早发布了新的文献求助10
4秒前
4秒前
个性的天奇完成签到,获得积分20
4秒前
5秒前
Luo完成签到 ,获得积分10
5秒前
6秒前
热心小蕊发布了新的文献求助10
6秒前
111发布了新的文献求助10
6秒前
7秒前
10秒前
完美世界应助squeak采纳,获得10
10秒前
M二十四发布了新的文献求助10
10秒前
Allez完成签到,获得积分10
12秒前
bkagyin应助JOE采纳,获得10
12秒前
13秒前
核桃应助明亮的犀牛采纳,获得10
13秒前
刘营营完成签到,获得积分10
13秒前
13秒前
15秒前
个性的天奇关注了科研通微信公众号
15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
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Governing Growth: Us Industrial Policy from Hamilton to Trump 500
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
Synthesis of P-Chiral Phosphine Ligands and Their Applications in Asymmetric Catalysis 400
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 7624884
求助须知:如何正确求助?哪些是违规求助? 9199878
关于积分的说明 19724179
捐赠科研通 7195890
什么是DOI,文献DOI怎么找? 3273588
关于科研通互助平台的介绍 2435754
邀请新用户注册赠送积分活动 2269423