Department of Physics, Optoelectronics and Energy, Jiangsu Key Laboratory of Thin Films and ‡Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-based Functional Materials and Devices, Collaborative Innovation Center of Suzhou Nano Science and Technology, Soochow University , Suzhou 215006, China.
ACS Appl Mater Interfaces. 2017 Feb 22;9(7):6123-6129. doi: 10.1021/acsami.6b15854. Epub 2017 Feb 9.
Water splitting in a photoelectrochemical cell, which converts sunlight into hydrogen energy, has recently received intense research. Silicon is suitable as a viable light-harvesting material for constructing such cell; however, there is a need to improve its stability and explore a cheap and efficient cocatalyst. Here we fabricate highly efficient and stable photocathodes by integrating crystalline MoS catalyst with ∼2 nm AlO protected np-Si. AlO acts as a protective and passivative layer of the Si surface, while the sputtering method using a MoS target along with a postannealing leads to a vertically standing, conformal, and crystalline nano-MoS layer on AlO/np-Si photocathode. Efficient (0.4 V vs RHE onset potential and 35.6 mA/cm saturated photocurrent measured under 100 mA/cm Xe lamp illumination) and stable (above 120 h continuous water splitting) photocathode was obtained, which opens the door for the MoS catalyst to be applied in photoelectrochemical hydrogen evolution in a facile and scalable way.
光电化学池中的水分解将阳光转化为氢能,最近受到了强烈的研究关注。硅是一种适合构建这种电池的可行的光收集材料;然而,需要提高其稳定性并探索廉价且高效的共催化剂。在这里,我们通过将结晶 MoS 催化剂与约 2nm AlO 保护的 np-Si 集成来制造高效稳定的光电阴极。AlO 作为 Si 表面的保护和钝化层,而使用 MoS 靶材的溅射方法以及随后的退火导致垂直站立、共形且结晶的纳米 MoS 层在 AlO/np-Si 光电阴极上。获得了高效(相对于 RHE 起始电位为 0.4V,在 100mA/cm Xe 灯照射下测量的饱和光电流为 35.6mA/cm)和稳定(超过 120 小时连续水分解)的光电阴极,这为 MoS 催化剂以简单且可扩展的方式应用于光电化学析氢开辟了道路。