Department of Chemistry, University of Southern California , Los Angeles, California 90089, United States.
J Am Chem Soc. 2015 Nov 4;137(43):13740-3. doi: 10.1021/jacs.5b07020. Epub 2015 Oct 27.
Solar-driven hydrogen evolution from water has emerged as an important methodology for the storage of renewable energy in chemical bonds. Efficient and practical clean-energy devices for electrochemical or photoelectrochemical splitting of water require the immobilization of stable and active hydrogen-evolving catalysts onto electrode or photocathode materials, which remains a significant challenge. Here we show that cobalt(II) reacts with benzene-1,2,4,5-tetrathiol in the presence of base to form a cobalt dithiolene polymer 1. The generated polymer is immobilized onto glassy carbon electrodes (GCE) to generate a metal-organic surface (MOS 1|GCE), which displays efficient H2-evolving activity and stability in acidic aqueous solutions. Moreover, the generated polymer is integrated with planar p-type Si to generate very efficient photocathode materials (MOS 1|Si) for solar-driven hydrogen production from water. Photocurrents up to 3.8 mA/cm(2) at 0 V vs RHE were achieved under simulated 1 Sun illumination. MOS 1|Si photocathodes operate at potentials 550 mV more positive than MOS 1|GCE cathodes to reach the same activity for H2 evolution from water (1 mA/cm(2)).
太阳能驱动的水分解制氢已成为将可再生能源以化学键形式储存的重要方法。电化学或光电化学水分解的高效、实用清洁能源器件需要将稳定、活性的析氢催化剂固定在电极或光阴极材料上,这仍然是一个重大挑战。在这里,我们展示了在碱性条件下,钴(II)与苯-1,2,4,5-四硫醇反应生成钴二硫烯聚合物 1。生成的聚合物被固定在玻碳电极(GCE)上,生成金属-有机表面(MOS 1|GCE),在酸性水溶液中显示出高效的析氢活性和稳定性。此外,生成的聚合物与平面 p 型 Si 集成,生成非常高效的光阴极材料(MOS 1|Si),用于太阳能驱动水分解制氢。在模拟的 1 个太阳光照下,实现了高达 3.8 mA/cm(2)的光电流。MOS 1|Si 光阴极的工作电位比 MOS 1|GCE 阴极正 550 mV,以达到相同的水析氢活性(1 mA/cm(2))。