Toupin J, Strub H, Kressmann S, Boudot M, Artero V, Laberty-Robert Ch
Sorbonne Universités, UPMC Univ Paris 06, CNRS, Collège de France, Laboratoire de Chimie de la Matière Condensée de Paris, 4 place Jussieu, Paris 75005, France.
Phys Chem Chem Phys. 2017 Nov 22;19(45):30675-30682. doi: 10.1039/c7cp05122k.
The generation of hydrogen from water and sunlight offers a promising approach for producing scalable and sustainable carbon free fuels. One of the challenges of solar-to-fuel technology is the design of efficient, long-lasting and low-cost photocathodes, which are responsible for absorbing sunlight and driving catalytic hydrogen evolution. We report on the protection of a Cu/CuO/CuO photoelectrode against photocorrosion by a 200-300 nm-thick BaTiO perovskite layer, deposited using the sol-gel method. This photoelectrode mediates H production with a current density of ∼3.1 mA cm at 0 V versus RHE under 3 Sun irradiation and in a pH = 6 aqueous electrolyte. While the unprotected Cu/CuO/CuO photoelectrodes show a rapid decay of activity, the BaTiO-protected photoelectrodes exhibit ∼10% current decay over 20 min.
利用水和阳光制氢为生产可扩展且可持续的无碳燃料提供了一种很有前景的方法。太阳能到燃料技术面临的挑战之一是设计高效、耐用且低成本的光电阴极,光电阴极负责吸收阳光并驱动催化析氢反应。我们报道了通过溶胶 - 凝胶法沉积的200 - 300纳米厚的钛酸钡钙钛矿层对铜/氧化铜/氧化铜光电极进行光腐蚀防护。该光电极在3倍太阳光照射下、相对于可逆氢电极(RHE)为0 V以及pH = 6的水性电解质中,以约3.1 mA/cm²的电流密度介导产氢。未受保护的铜/氧化铜/氧化铜光电极的活性迅速衰减,而经钛酸钡保护的光电极在20分钟内电流衰减约10%。