纳米片
光催化
异质结
氢氧化物
吸收(声学)
材料科学
带隙
热液循环
制氢
水热合成
锌
化学工程
化学
氢
无机化学
纳米技术
催化作用
光电子学
复合材料
冶金
有机化学
工程类
生物化学
作者
Jingjing Shi,Shuangde Li,Fengming Wang,Lina Gao,Yanmei Li,Xiaorang Zhang,Jun Lu
出处
期刊:Dalton Transactions
[The Royal Society of Chemistry]
日期:2019-01-01
卷期号:48 (10): 3327-3337
被引量:33
摘要
Zinc cadmium sulfide solid solution (ZnxCd1-xS) photocatalysts have received significant attention in energy and environmental applications because of their wide and strong visible light absorption range. However, the high photogenerated electron-hole pair recombination rate is an innate problem for their application. In this study, Cu2S/Zn0.67Cd0.33S (CZCS) nanosheet heterojunctions were fabricated by the in situ topotactic hydrothermal transformation of CuZnCdAl layered double hydroxide (LDH) precursors. Structural and morphological characterization indicated that the CZCS nanosheets were 2D/2D atomic-level in-plane heterojunctions with matched crystalline orientation because of their intergrowth structure originating from the topotactic sulfurization of CuZnCdAl LDH precursors. This in-plane intergrowth structure enhanced the separation of photogenerated electron-hole pairs based on a direct Z-scheme mechanism, which, in addition to providing a wide light absorption range and appropriate flat band potential, endowed excellent photocatalytic hydrogen production at the rate of 15.27 mmol h-1 g-1 (about 3.82 times that of pure Zn0.67Cd0.33S) from water splitting under visible light irradiation without the additive Pt cocatalysts. This photocatalyst with a superior photocatalytic activity and cycling stability can serve as a hopeful candidate for applications in the energy and environment field.
科研通智能强力驱动
Strongly Powered by AbleSci AI