Rosman Nurul Nabila, Mohamad Yunus Rozan, Jeffery Minggu Lorna, Arifin Khuzaimah, Kassim Mohammad B, Mohamed Mohd Ambri
Fuel Cell Institute, Universiti Kebangsaan Malaysia, Malaysia.
Nanotechnology. 2020 Oct 22;32(3):035705. doi: 10.1088/1361-6528/abbea9.
Two-dimensional materials have attracted intensive attention recently due to their unique optical and electronic properties and their promising applications in water splitting and solar cells. As a representative layer-structured of transition metal dichalcogenides, MoS has attracted considerable devotion owing to its exceptional photo and electro properties. Here, we show that the chemical vapour deposition (CVD) growth of MoS on Si photocathode and graphene/Si photocathode can be used to prepare photoelectrocatalysts for water splitting. We explore a bottom-up method to grow vertical heterostructures of MoS and graphene by using the two-step CVD. Graphene is first grown through ambient-pressure CVD on a Cu substrate and then transferred onto SiO/Si substrate by using the chemical wet transfer followed by the second CVD method to grow MoS over the graphene/SiO/Si. The effect of the growth temperatures of MoS is studied, and the optimum temperature is 800 °C. The MoS produced at 800 °C has the highest photocurrent density at -0.23 mA cm in 0.5 M NaSO and -0.51 mA cm in 0.5 M HSO at -0.8 V versus Ag/AgCl. The linear sweep voltammetry shows that MoS in 0.5 M HSO has about 55% higher photocurrent density than MoS in NaSO due to the higher concentration of protons (H) in the HSO electrolyte solution. Protons are reduced to H at lower overvoltage and hydrogen generation is thus enhanced at higher photocurrent density. MoS/graphene/SiO/Si (MGS) has -0.07 mA cm at -0.8 V versus Ag/AgCl of photocurrent density, which is 70% lower than that of bare MoS because MGS is thicker compared with MoS. Thus, MoS has potential as a photocatalyst in photoelectrochemical water splitting. The structure and the morphology of MoS play an important role in determining the photocurrent performance.
二维材料因其独特的光学和电子特性以及在水分解和太阳能电池方面的潜在应用,近年来受到了广泛关注。作为过渡金属二硫属化物的典型层状结构,MoS由于其优异的光电性能而备受关注。在此,我们展示了在硅光电阴极和石墨烯/硅光电阴极上通过化学气相沉积(CVD)生长MoS可用于制备水分解的光电催化剂。我们探索了一种自下而上的方法,通过两步CVD生长MoS和石墨烯的垂直异质结构。首先通过常压CVD在铜衬底上生长石墨烯,然后使用化学湿法转移将其转移到SiO/Si衬底上,接着采用第二种CVD方法在石墨烯/SiO/Si上生长MoS。研究了MoS生长温度的影响,最佳温度为800℃。在800℃下制备的MoS在相对于Ag/AgCl为-0.8V时,在0.5M NaSO中的光电流密度最高为-0.23mA/cm²,在0.5M HSO中的光电流密度为-0.51mA/cm²。线性扫描伏安法表明,由于HSO电解质溶液中质子(H⁺)浓度较高,在0.5M HSO中的MoS光电流密度比在NaSO中的MoS高约55%。质子在较低过电位下还原为H₂,从而在较高光电流密度下增强了氢气的产生。MoS/石墨烯/SiO/Si(MGS)在相对于Ag/AgCl为-0.8V时的光电流密度为-0.07mA/cm²,比裸MoS低70%,因为MGS比MoS更厚。因此,MoS在光电化学水分解中具有作为光催化剂的潜力。MoS的结构和形态在决定光电流性能方面起着重要作用。