College of Materials Science and Engineering, Zhengzhou University , Zhengzhou 450052, China.
Centre for Clean Environment and Energy and Griffith School of Environment, Griffith University , Nathan, QLD 4111, Australia.
ACS Nano. 2016 Feb 23;10(2):2903-9. doi: 10.1021/acsnano.6b00001. Epub 2016 Feb 4.
Molybdenum disulfide (MoS2) is a promising non-precious-metal catalyst, but its performance is limited by the density of active sites and poor electrical transport. Its metallic 1T phase possesses higher photoelectrocatalytic activity. Thus, how to efficiently increase the concentration of the 1T phase in the exfoliated two-dimensiaonal (2D) MoS2 nanosheets is an important premise. In this work, we propose a strategy to prepare a 2D heterostructure of MoS2 nanosheets using supercritical CO2-induced phase engineering to form metallic 1T-MoS2. Theoretical calculations and experimental results demonstrate that the introduced CO2 in the 2H-MoS2 host can prompt the transformation of partial 2H-MoS2 lattices into 1T-MoS2. Moreover, the electrical coupling and synergistic effect between 2H and 1T phases can greatly facilitate the efficient electron transfer from the active sites of MoS2, which significantly improves the photocatalytic performance.
二硫化钼(MoS2)是一种很有前途的非贵金属催化剂,但它的性能受到活性位密度和较差的电子输运的限制。其金属 1T 相具有更高的光电催化活性。因此,如何有效地增加剥离二维(2D)MoS2 纳米片中 1T 相的浓度是一个重要前提。在这项工作中,我们提出了一种使用超临界 CO2 诱导相工程制备 MoS2 纳米片 2D 异质结构的策略,以形成金属 1T-MoS2。理论计算和实验结果表明,在 2H-MoS2 主体中引入的 CO2 可以促使部分 2H-MoS2 晶格转化为 1T-MoS2。此外,2H 和 1T 相之间的电耦合和协同作用可以极大地促进 MoS2 活性位的有效电子转移,从而显著提高光催化性能。