光电阴极
光电流
光电化学电池
串联
化学计量学
能量转换效率
太阳能电池
材料科学
光电化学
可逆氢电极
相(物质)
纳米晶
光电子学
电极
化学
分析化学(期刊)
纳米技术
电解质
电化学
电子
工作电极
物理化学
物理
量子力学
复合材料
有机化学
色谱法
作者
Elena Alfonso‐González,Marta Liras,Mengjiao Wang,Ignacio J. Villar‐García,Luca De Trizio,Mariam Barawi,Víctor A. de la Peña O’Shea
标识
DOI:10.1016/j.solmat.2022.112050
摘要
In this work we present the design, assembly and characterization of a tandem photoelectrochemical (PEC) cell based on two different crystallographic phases of sub-stoichiometric copper telluride nanocrystals (NCs). The first one, a pseudo-cubic phase, pc-Cu2-xTe, is characterized by positive photocurrents, while the second one, a hexagonal phase, h-Cu2-xTe, favors negative ones. Taking advantage of the different optoelectronic properties of the two Cu2-xTe structures, we prepared a PEC cell composed of a hybrid pc-Cu2-xTe/TiO2 photoanode, with TiO2 acting as a light absorber and electron selective layer, and a h-Cu2-xTe/CuI photocathode, with CuI behaving as a photo-absorber and hole selective layer. The tandem PEC cell shows a photocurrent density of ∼0.5 mA/cm2 when measured in a 2-electrode configuration without any co-catalyst. Finally, to test the PEC cell performance for the hydrogen evolution reaction (HER), a thin film of Pt was deposited on top of the photocathode and ∼7 μmol of hydrogen were obtained at 0.6 V in a 1-h experiment, reaching a photocurrent of 1 mA/cm2 with no losses.
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