光催化
载流子
纳米复合材料
材料科学
可见光谱
纳米颗粒
氢
纳米技术
量子点
制氢
纳米线
光化学
化学工程
化学
催化作用
光电子学
有机化学
工程类
作者
Chunhe Li,Hongmei Wang,Sara Bonabi Naghadeh,Jin Z. Zhang,Pengfei Fang
标识
DOI:10.1016/j.apcatb.2018.01.038
摘要
Uniform one-dimensional (1D) NiS/CdS nanocomposites have been fabricated using CdS nanowires (NWs) and NiS nanoparticles as building blocks through two-pot solvothermal synthesis. The synergistic interaction between CdS and NiS, stemming from their intimate contact, efficiently enhanced charge carrier separation, with the NiS, as a non-noble metal cocatalyst, enriching the active sites for H2 production from water. Consequently, compared with pristine CdS NWs, the 1D NiS/CdS nanocomposite exhibited improved visible light reactivity in the generation of H2. The activity of NiS/CdS with 20 mol% of NiS loading, under the coexistence of lactic acid and lignin as hole scavengers, is 5041 times that of pristine CdS, with an apparent quantum efficiency (AQE) of 44.9% for H2 generation. To gain deeper insight into the mechanism behind the enhanced performance, ultrafast dynamics studies based on femtosecond transient absorption (TA) techniques have been applied to probe the charge carrier dynamics. The results reveal that presence of 0.2 molar ratio of NiS improved the average charge carrier lifetime of CdS NWs by 97 times, potentially leading to more efficient charge separation and transfer. However, further increasing the NiS loading resulted in shorter lifetime or faster electron-hole recombination, attributed to aggregation of NiS nanoparticles. The dynamics results agree well with the photocatalytic results in that the longer charge carrier lifetime correlates with improved performance in hydrogen evolution. This work demonstrates a simple approach to controlled synthesis of well-shaped 1D nanocomposite photocatalysts for visible-light driven energy conversion, particularly involving the use of biomass.
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