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首页> 外文期刊>Carbon: An International Journal Sponsored by the American Carbon Society >Enhanced visible/near-infrared light harvesting and superior charge separation via 0D/2D all-carbon hybrid architecture for photocatalytic oxygen evolution
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Enhanced visible/near-infrared light harvesting and superior charge separation via 0D/2D all-carbon hybrid architecture for photocatalytic oxygen evolution

机译:通过0D / 2D全碳混合架为光催化氧气进化,增强可见/近红外光收集和优质电荷分离

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Since the water splitting rate-limiting oxygen evolution remains sluggish, engineering a rational architecture for photocatalysts to fulfill water oxidation needs becomes a vital issue. Here, we detail a 0D/2D all-carbon hybrid strategy for constructing a heterostructure of carbon dots (CDots) and reduced graphene oxide (rGO) to enhance the photocatalytic water oxidation of monoclinic-BiVO4 nanosheets (CBrG). Given the visible-light-harvesting ability and up-conversion characteristics of 0D CDots, more photogenerated electron-hole pairs participated in water oxidation under visible and near-infrared light irradiation. Meanwhile, 0D CDots behaved as electron acceptors on 2D rGO to suppress the recombination of electron-hole pairs. This nature licenses for the feasible electron transfer from excited m-BiVO4 to 0D CDots via electron transfer channels of 2D rGO, facilitating the separated holes to migrate onto the m-BiVO4 surface for water oxidation. Compared with the rGO decorated m-BiVO4 nanosheets (BrG), these merits endow the CBrG with an over 212% enhancement in O-2 yield under visible light irradiation as well as notable O-2 yield under near-infrared light irradiation, and a 1.57-fold increase in apparent quantum efficiency. The enhancement is also verified by the significant growth of center dot OH radicals derived from OH-/H2O oxidation and center dot OOH/center dot O-2(-) radicals originated from O-2 reduction. This work paves a new way for the 0D/2D all-carbon hybrid architecture applied in solar energy conversion. (C) 2020 Elsevier Ltd. All rights reserved.
机译:由于水分裂速率限制氧气进化仍然缓慢,工程为实现水氧化需要的光催化剂的合理建筑成为一个重要问题。这里,我们详细介绍了一种用于构建碳点(Cdots)的异质结构和还原氧化石墨烯(RGO)的0d / 2d全碳杂化策略,以增强单斜晶型-bivo4纳米片(CBRG)的光催化水氧化。鉴于0D CDOTS的可见光能力和上转换特性,在可见光和近红外光照射下,更多的光静电电子空穴对参与水氧化。同时,0D CDOTS在2D RGO上表现为电子受体,抑制电子孔对的重组。这种自然许可证,可行电子从激发的M-BIVO4到0D Cdots通过电子传递通道的2D RGO的电子传递通道转移,便于分离的孔迁移到用于水氧化的M-BIVO4表面上。与RGO装饰的M-BIVO4纳米蛋白酶(BRG)相比,这些优点在可见光照射下的O-2产率上超过212%增强,以及近红外光照射下的值得注意的O-2产量,以及表观量子效率为1.57倍。还通过从OH-/ H 2 O氧化的中心点OH基团的显着生长来验证增强,源自O-2还原的中心点OH /中心点O-2( - )基团。这项工作为0D / 2D全碳混合体系结构铺平了一种在太阳能转换中的新方法。 (c)2020 elestvier有限公司保留所有权利。

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