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Engineering 2D Metal-Organic Framework/MoS_2 Interface for Enhanced Alkaline Hydrogen Evolution

机译:工程2D金属 - 有机框架/ MOS_2接口,用于增强碱性氢气进化

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摘要

2D metal-organic frameworks (MOFs) have been widely investigated for electrocatalysis because of their unique characteristics such as large specific surface area, tunable structures, and enhanced conductivity. However, most of the works are focused on oxygen evolution reaction. There are very limited numbers of reports on MOFs for hydrogen evolution reaction (HER), and generally these reported MOFs suffer from unsatisfactory HER activities. In this contribution, novel 2D Co-BDC/MoS_2 (BDC stands for 1,4-benzenedicarboxylate, C_8H_4O_4) hybrid nanosheets are synthesized via a facile sonication-assisted solution strategy. The introduction of Co-BDC induces a partial phase transfer from semiconducting 2H-MoS_2 to metallic 1T-MoS_2. Compared with 2H-MoS_2, 1T-MoS_2 can activate the inert basal plane to provide more catalytic active sites, which contributes significantly to improving HER activity. The well-designed Co-BDC/MoS_2 interface is vital for alkaline HER, as Co-BDC makes it possible to speed up the sluggish water dissociation (rate-limiting step for alkaline HER), and modified MoS_2 is favorable for the subsequent hydrogen generation step. As expected, the resultant 2D Co-BDC/ MoS_2 hybrid nanosheets demonstrate remarkable catalytic activity and good stability toward alkaline HER, outperforming those of bare Co-BDC, MoS_2, and almost all the previously reported MOF-based electrocatalysts.
机译:由于其独特的特性,例如大的比表面积,可调谐结构和增强的导电性,因此,已被广泛研究了电常放的金属有机框架(MOF)被广泛研究了电常分。然而,大部分作品都集中在氧气进化反应上。关于氢进化反应的MOF数量非常有限数量的报道,并且通常这些报告的MOFS患有不满意的她的活动。在这一贡献中,通过容易超声处理辅助溶液策略合成了新的2D CO-BDC / MOS_2(BDC代表1,4-苯并二羧酸甲酯,C_8H_4O_4)杂交纳米。 Co-BDC的引入引起从半导体2H-MOS_2到金属1T-MOS_2的部分相移。与2H-MOS_2相比,1T-MOS_2可以激活惰性基底平面以提供更多的催化活性位点,这有助于改善她的活性。精心设计的CO-BDC / MOS_2界面对于碱性的界面至关重要,因为CO-BDC使得可以加速缓慢的水解离(碱性碱性的步骤),并且改性MOS_2有利于随后的氢气产生步。如所预期的,所得2D CO-BDC / MOS_2杂交纳米液表现出显着的催化活性和对碱性的良好稳定性,优于裸CO-BDC,MOS_2,以及几乎所有先前报告的基于MOF基电催化剂。

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