光催化
可见光谱
聚合
X射线光电子能谱
分解水
聚合物
载流子
纳米颗粒
化学
辐照
材料科学
光化学
化学工程
纳米技术
催化作用
复合材料
光电子学
有机化学
核物理学
工程类
物理
作者
Pengfei Xia,Mingjin Liu,Bei Cheng,Bei Cheng,Liuyang Zhang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2018-05-18
卷期号:6 (7): 8945-8953
被引量:202
标识
DOI:10.1021/acssuschemeng.8b01300
摘要
Photocatalytic water splitting is a promising strategy to convert solar energy into chemical energy. Herein, a series of g-C3N4/polydopamine (g-C3N4/PDA) composites were successfully fabricated by in situ polymerization of dopamine on the g-C3N4 surface. Among all the as-prepared composites, the best photocatalytic hydrogen evolution rate of the as-prepared composites was up to 69 μmol h–1 under the irradiation of visible light (λ > 420 nm), which was about 4.5 times than that of pristine g-C3N4 (16 μmol h–1). The enhancement of photocatalytic H2 evolution is reasonably attributed to the markedly enhanced light harvesting, broadened spectral response range and low onset potential of H2 production, as well as effective separation and rapid transportation of photogenerated charge carriers. More importantly, the surface modification of g-C3N4 by a small amount of PDA can effectively inhibit the overgrowth of Pt nanoparticles (NPs) during the photocatalytic reactions, which promotes the photoelectron injection and better photocatalytic activity. This work should provide a new insight into preparing metal-free polymer–polymer composites with effective solar energy conversion.
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