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Plasmon-Assisted Water Splitting Using Two Sides of the Same SrTiO3 Single-Crystal Substrate: Conversion of Visible Light to Chemical Energy

机译:使用同一SrTiO3单晶衬底的两面进行等离子体辅助水分解:将可见光转换为化学能

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摘要

A plasmon-induced water splitting system that operates under irradiation by visible light was successfully developed; the system is based on the use of both sides of the same strontium titanate (SrTiO3) single-crystal substrate. The water splitting system contains two solution chambers to separate hydrogen (H2) and oxygen (O2). To promote water splitting, a chemical bias was applied by regulating the pH values of the chambers. The quantity of H2 evolved from the surface of platinum, which was used as a reduction co-catalyst, was twice the quantity of O2 evolved from an Au-nano-structured surface. Thus, the stoichiometric evolution of H2 and O2 was clearly demonstrated. The hydrogen-evolution action spectrum closely corresponds to the plasmon resonance spectrum, indicating that the plasmon-induced charge separation at the Au/SrTiO3 interface promotes water oxidation and the subsequent reduction of a proton on the backside of the SrTiO3 substrate. The chemical bias is significantly reduced by plasmonic effects, which indicates the possibility of constructing an artificial photosynthesis system with low energy consumption.
机译:已成功开发了在可见光照射下运行的等离子体激元诱导的水分解系统;该系统基于使用同一钛酸锶(SrTiO3)单晶衬底的两面。分水系统包含两个溶液室,以分离氢气(H2)和氧气(O2)。为了促进水的分解,通过调节腔室的pH值来施加化学偏压。从用作还原助催化剂的铂表面放出的H2量是从金纳米结构表面放出的O2量的两倍。因此,清楚地证明了H2和O2的化学计量的演变。氢演化作用谱与等离振子共振谱紧密对应,表明在Au / SrTiO3界面处由等离激元引起的电荷分离促进了水的氧化,并随后促进了SrTiO3衬底背面的质子的还原。等离子体效应可显着降低化学偏差,这表明构建具有低能耗的人工光合作用系统的可能性。

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