首页> 外文期刊>International journal of hydrogen energy >Enhanced charge transfer for efficient photocatalytic H_2 evolution over UiO-66-NH_2 with annealed Ti_3C_2T_x MXenes
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Enhanced charge transfer for efficient photocatalytic H_2 evolution over UiO-66-NH_2 with annealed Ti_3C_2T_x MXenes

机译:增强的电荷转移,可通过退火的Ti_3C_2T_x MXene在UiO-66-NH_2上高效光催化H_2的演化

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The annealed Ti3C2Tx MXenes retained original layered morphology and gave rise to the formation of TiO2 is anticipated to achieve improved photocatalytic hydrogen evolution performance as a noble-metal-free co-catalyst. In this work, a novel Ti3C2/TiO2/UiO-66-NH2 hybrid was rationally designed for the first time by simply introducing annealed Ti3C2Tx MXenes over water-stable Zr-MOFs (UiO-66-NH2) precursors via a facile hydrothermal process. As expected, the rationally designed Ti3C2/TiO2/UiO-66-NH2 displayed significantly improvement in photocatalytic H-2 performance (1980 mu mol.h(-1).g(-2)) than pristine UiO-66-NH2 under simulated sunlight irradiation. The excellent photocatalytic HER activity can be attributed to the formation of multi-interfaces in Ti3C2/TiO2/UiO-66-NH2, including Ti3C2/TiO2/UiO-66-NH2, Ti3C2/TiO2 and Ti3C2/TiO2/UiO-66-NH2 interfaces, which constructed multiple pathways at the interfaces with Schottky junctions to accelerate the separation and transfer of charge carriers and endowed the accumulation of photo-generated electrons on the surface of Ti3C2. This work expanded the possibility of porous MOFs for the development of efficient photocatalytic water splitting using annealed MXenes. (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:经过退火的Ti3C2Tx MXenes保留了原始的层状形态,并形成了TiO2,作为无贵金属助催化剂,有望实现改善的光催化氢释放性能。在这项工作中,通过简单的水热过程,通过在水稳定的Zr-MOF(UiO-66-NH2)前驱体上简单地引入退火的Ti3C2Tx MXene,首次合理地设计了新颖的Ti3C2 / TiO2 / UiO-66-NH2杂化物。如预期的那样,在模拟条件下,合理设计的Ti3C2 / TiO2 / UiO-66-NH2显示出比原始UiO-66-NH2显着改善的光催化H-2性能(1980μmol.h(-1).g(-2))。阳光照射。优异的光催化HER活性可归因于Ti3C2 / TiO2 / UiO-66-NH2中多界面的形成,包括Ti3C2 / TiO2 / UiO-66-NH2,Ti3C2 / TiO2和Ti3C2 / TiO2 / UiO-66-NH2界面,在与肖特基结的界面处构造了多个路径,以加速电荷载流子的分离和转移,并赋予了光生电子在Ti3C2表面的积累。这项工作扩大了多孔MOF的可能性,以开发使用退火的MXene进行有效的光催化水分解。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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