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Promising Photocathodes Based on Non-noble Metal Catalysts of CoSe2 or CoS2 with Heterostructure of Si for Photoelectrochemical Hydrogen Evolution

机译:基于COSE2或COS2的非贵金属催化剂的有前途的光电阴极与SI的SI异质结构进行光电化学氢气进化

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In consideration with the upcoming energy crisis and current environmental issues, alternative and efficient green energy sources are urgently needed. In this respect, hydrogen is a very promising clean energy source, which can fulfill the energy demands. Photoelectrochemical (PEC) water splitting is a highly controlled approach to convert sunlight into clean and storable hydrogen and oxygen. A large scale effort has already been dedicated to find out this alternative and also to fulfill the dream by generating higher photocurrent density. However, the major problem in PEC system is that it is very hard for a single material to achieve all the requirements. Visible light-active materials suffer from photocorrosion, whereas wide-bandgap materials can be activated by UV light only. Higher photocurrents can be achieved by coupling two semiconductors with a type-II band alignment. Nevertheless, the problem of sluggish hydrogen and oxygen evolution reaction rate decreases the efficiency of a material. Another approach to solve this problem is to decorate the semiconductor surface with a suitable co-catalyst, which further lowers the overpotential by increasing the kinetics of photoexcited electrons.
机译:考虑到即将到来的能源危机和当前的环境问题,迫切需要替代和有效的绿色能源。在这方面,氢是一种非常有前景的清洁能源,可以满足能量需求。光电化学(PEC)水分裂是一种高度控制的方法,可以将阳光转化为清洁和可储存的氢气和氧气。大规模的努力已经致力于找出这种替代方案,并通过产生更高的光电流密度来实现梦想。然而,PEC系统的主要问题是单一材料非常努力实现所有要求。可见光活性物质患有光腐蚀,而宽带隙材料只能通过UV光激活。通过耦合具有II型带对准的两个半导体可以实现更高的光电流。然而,缓慢的氢气和氧气进化反应速率的问题降低了材料的效率。解决该问题的另一种方法是用合适的助催化剂装饰半导体表面,这通过增加光屏蔽电子的动力学进一步降低过电位。

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