光电流
光化学
光催化
光电阴极
材料科学
石墨烯量子点
量子点
罗丹明B
可见光谱
共价键
石墨烯
分解水
双极扩散
罗丹明
化学
光电子学
纳米技术
荧光
电子
光学
物理
催化作用
有机化学
量子力学
作者
Diptiman Dinda,Soo Young Park,Hyun Jun Lee,Sangyoon Oh,Soo Young Park
出处
期刊:Carbon
[Elsevier]
日期:2020-10-01
卷期号:167: 760-769
被引量:18
标识
DOI:10.1016/j.carbon.2020.06.041
摘要
Designing metal free photocatalyst for solar water splitting is an emerging field of research. Although graphene quantum dot (GQD) has been explored as a potential photocatalyst, their performance remains inherently limited by poor visible light absorption and p-type conductivity. To address this problem, we have covalently functionalized GQD with visible light active photosensitizer Rhodamine 123. It was found that this dye-sensitized GQD could make quite stabilized photocatalytic hydrogen evolution reaction (HER) under visible light irradiation, which is in striking contrast to the virtually inactive photocatalytic HER performance of control GQD without dye. Efficient photo-induced electron transfer from Rhodamine 123 to GQD and also the transformation of p type GQD to the n-p ambipolar semiconductor, both boosted by covalent bonding, are responsible for such high photocatalytic HER performance. Observation of negative photocurrent at zero bias voltage during transient photocurrent measurement, also suggests its promising potential in the metal free photocathode system to achieve photoelectrochemical H2 production.
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