首页> 外文期刊>Journal of Materials Chemistry, C. materials for optical and electronic devices >CdSe quantum dot/white graphene hexagonal porous boron nitride sheet (h-PBNs) heterostructure photocatalyst for solar driven H-2 production
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CdSe quantum dot/white graphene hexagonal porous boron nitride sheet (h-PBNs) heterostructure photocatalyst for solar driven H-2 production

机译:CDSE量子点/白色石墨烯六边形多孔硼氮化物片(H-PBNS)异质结构光催化剂用于太阳驱动H-2生产

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In the world of photocatalytic hydrogen (H-2) evolution two-dimensional (2D) nanomaterials have attracted widespread attention owing to their high surface area, abundant active sites, and excellent photogenerated charge separation properties. In the present work, CdSe QDs coupled with different weight percent of ultra-thin layered hexagonal porous boron nitride sheets (h-PBNs) functionalized with 3-mercaptopropionic acid (3-MPA) have been synthesized and studied for photocatalytic hydrogen (H-2) evolution reaction. The h-PBNs/CdSe heterostructure with 30 wt% optimized loading shows an excellent photocatalytic H-2 evolution of 25 128 mu mol g(-1) h(-1) which is 18.6 times higher than that offered by solely functionalized h-PBNs. The remarkable photocatalytic H-2 evolution benefits are anticipated to be attained owing to factors like the high specific surface area of porous h-PBNs (409 m(2) g(-1)), which allows a uniform deposition of CdSe QDs on the surface providing more adsorption sites, and the presence of the thiol group on 3-MPA which strongly tethers the CdSe QDs to the h-PBNs which effectively reduces the photogenerated charge recombination as confirmed by PL and EIS studies. The 30% h-PBNs/CdSe photoelectrode shows excellent photoelectrochemical (PEC) performance. The photocurrent density achieved by the 30% h-PBNs/CdSe heterostructure is 1.2 mA cm(-2) at 1.2 V vs. Ag/AgCl, which is 4.13-fold and 2.56-fold higher compared to that achieved by h-PBNs and CdSe QDs. This study reveals that the 30% h-PBNs/CdSe heterostructure forms the type II heterojunction which offers new insight into the development of a heterojunction system for effective photocatalytic H-2 evolution from water.
机译:在光催化氢(H-2)演化领域,二维(2D)纳米材料因其高比表面积、丰富的活性中心和优异的光生电荷分离性能而受到广泛关注。在本工作中,我们合成了与不同重量百分比的超薄层状六方多孔氮化硼片(h-PBN)偶联的CdSe量子点,并对其进行了光催化析氢(h-2)反应的研究。优化负载量为30 wt%的h-PBNs/CdSe异质结构显示出25 128μmol g(-1)h(-1)的优良光催化h-2演化,比单独功能化的h-PBNs高18.6倍。由于多孔H-PBN(409 m(2)g(-1))的高比表面积等因素,可以在表面上均匀沉积CdSe量子点,从而提供更多的吸附位置,因此有望获得显著的光催化H-2析出效益,3-MPA上的硫醇基团将CdSe量子点与h-PBN紧密相连,从而有效地减少了光生电荷复合,PL和EIS研究证实了这一点。30%h-PBNs/CdSe光电极具有优异的光电化学性能。与Ag/AgCl相比,30%h-PBNs/CdSe异质结构在1.2V下获得的光电流密度为1.2mA cm(-2),比h-PBNs和CdSe量子点获得的光电流密度高4.13倍和2.56倍。这项研究表明,30%的h-PBNs/CdSe异质结构形成了II型异质结,这为从水中有效光催化h-2释放的异质结系统的开发提供了新的见解。

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