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硅负载非晶态钴钼硫化物催化剂作为高效光解水产氢催化剂。

Silicon decorated with amorphous cobalt molybdenum sulfide catalyst as an efficient photocathode for solar hydrogen generation.

机构信息

†Energy Research Institute at Nanyang Technological University (ERI@N), 50 Nanyang Drive, Singapore 637553.

‡Solar Fuels Laboratory, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798.

出版信息

ACS Nano. 2015 Apr 28;9(4):3829-36. doi: 10.1021/nn506819m. Epub 2015 Mar 26.

Abstract

The construction of viable photoelectrochemical (PEC) devices for solar-driven water splitting can be achieved by first identifying an efficient independent photoanode for water oxidation and a photocathode for hydrogen generation. These two photoelectrodes then must be assembled with a proton exchange membrane within a complete coupled system. Here we report the preparation of a Si/a-CoMoSx hybrid photocathode which shows impressive performance (onset potential of 0.25 V vs RHE and photocurrent jsc of 17.5 mA cm(-2) at 0 V vs RHE) in pH 4.25 phosphate solution and under simulated AM 1.5 solar illumination. This performance is among the best reported for Si photocathodes decorated with noble-metal-free catalysts. The electrode preparation is scalable because it relies on a photoassisted electrodeposition process employing an available p-type Si electrode and Co(MoS4)2 precursor. Investigation of the mechanism of the Si/a-CoMoSx electrode revealed that under conditions of H2 photogeneration this bimetallic sulfide catalyst is highly efficient in extracting electrons from illuminated Si and subsequently in reducing protons into H2. The Si/a-CoMoSx photocathode is functional over a wide range of pH values, thus making it a promising candidate for the construction of a complete solar-driven water splitting PEC device.

摘要

构建用于太阳能驱动水分解的可行光电化学(PEC)器件,可以通过首先确定用于水氧化的高效独立光阳极和用于产氢的光阴极来实现。然后,这两个光电必须在完整的耦合系统内与质子交换膜组装在一起。在这里,我们报告了 Si/a-CoMoSx 杂化光阴极的制备,该光阴极在 pH 值为 4.25 的磷酸盐溶液中和在模拟 AM 1.5 太阳光照下表现出令人印象深刻的性能(起始电位为 0.25 V 相对于 RHE,在 0 V 相对于 RHE 时的光电流 jsc 为 17.5 mA cm(-2))。这种性能在使用无贵金属催化剂修饰的 Si 光阳极中属于最佳性能之一。该电极的制备具有可扩展性,因为它依赖于一种光辅助电沉积过程,该过程使用可用的 p 型 Si 电极和 [Co(MoS4)2](2-)前体。对 Si/a-CoMoSx 电极的机理研究表明,在 H2 光生成的条件下,这种双金属硫化物催化剂能够从被照亮的 Si 中高效地提取电子,随后将质子还原为 H2。Si/a-CoMoSx 光阴极在很宽的 pH 值范围内都具有功能,因此是构建完整太阳能驱动水分解 PEC 器件的有前途的候选材料。

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