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首页> 外文期刊>Journal of Colloid and Interface Science >In situ growth of CdS quantum dots on phosphorus-doped carbon nitride hollow tubes as active 0D/1D heterostructures for photocatalytic hydrogen evolution
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In situ growth of CdS quantum dots on phosphorus-doped carbon nitride hollow tubes as active 0D/1D heterostructures for photocatalytic hydrogen evolution

机译:在磷掺杂的碳氮化空心管上的CDS量子点的原位生长为活性0d / 1d异质结构,用于光催化氢气进化

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CdS quantum dots (QDs) were decorated onto phosphorus-doped hexagonal g-C3N4 tube (P-CNT) to form a novel high-preformance photocatalyst (CdS QDs/P-CNT) via an in-situ oil bath approach. The ultra-small CdS QDs with the average diameter of similar to 9 nm are homogeneously anchored on the both external and internal surface of P-CNT hollow channel (similar to 25 mu m), yielding a type of zero-dimensional (0D)/one-dimensional (1D) heterojunction. The CdS QDs/P-CNT-1 exhibits the maximum photocatalytic H-2 evolution rate of 1579 mu mol h(-1) g(-1) under visible-light irradiation, which is 31.6, 6.8, 4.7 and 3.1 times higher than P-CNT, CdS, CdS/BCN and CdS/CNT, respectively. The improved photocatalytic activity of CdS QDs/P-CNT is primarily attributed to large surface area, P doping and formed 0D/1D heterojunction, which can broaden the light absorption, narrow the band gap, activate the H2O molecule and promote the spatial charge separation. Moreover, the DFT calculation coupled with experiment (Mott-Schottky curves) illustrates the electron transfer behavior of CdS QDs/P-CNT, showing that the Cd-1 site should be the main active center and P doping is beneficial to increase H-2 production. This work provides a new strategy to design of highly active 0D/1D photocatalyst for photocatalytic H-2 production. (C) 2020 Elsevier Inc. All rights reserved.
机译:将CDS量子点(QDS)装饰到磷掺杂的六方G-C3N4管(P-CNT)上,以通过原位油浴方法形成新的高预比率光催化剂(CDS QDS / P-CNT)。平均直径与9nm的平均直径相似的超小Cds QD在P-CNT中空通道(类似于25μm)的外部和内表面上均匀锚定,产生一种零维(0d)/一维(1D)异质结。 CDS QDS / P-CNT-1在可见光照射下表现出1579μmolH(-1)G(-1)的最大光催化H-2演化速率,比31.6,6.8,4.7和3.1倍高P-CNT,CD,CDS / BCN和CDS / CNT。 CDS QDS / P-CNT的改善的光催化活性主要归因于大表面积,P掺杂和形成的0d / 1d异质结,其能够宽光吸收,窄带隙,激活H2O分子并促进空间电荷分离。此外,与实验(Mott-Schottky曲线)耦合的DFT计算说明了CDS QDS / P-CNT的电子转移行为,表明CD-1位点应该是主动中心,P掺杂有利于增加H-2生产。这项工作为光催化H-2生产的高活性0d / 1d光催化剂设计了一种新的策略。 (c)2020 Elsevier Inc.保留所有权利。

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