Hefei National Laboratory of Physical Science at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026, China.
Hefei National Laboratory of Physical Science at the Microscale, University of Science and Technology of China, Hefei, Anhui 230026, China and Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026, China.
Phys Rev Lett. 2014 Jan 10;112(1):018301. doi: 10.1103/PhysRevLett.112.018301. Epub 2014 Jan 8.
Highly efficient solar energy utilization is very desirable in photocatalytic water splitting. However, until now, the infrared part of the solar spectrum, which constitutes almost half of the solar energy, has not been used, resulting in significant loss in the efficiency of solar energy utilization. Here, we propose a new mechanism for water splitting in which near-infrared light can be used to produce hydrogen. This ability is a result of the unique electronic structure of the photocatalyst, in which the valence band and conduction band are distributed on two opposite surfaces with a large electrostatic potential difference produced by the intrinsic dipole of the photocatalyst. This surface potential difference, acting as an auxiliary booster for photoexcited electrons, can effectively reduce the photocatalyst's band gap required for water splitting in the infrared region. Our electronic structure and optical property calculations on a surface-functionalized hexagonal boron-nitride bilayer confirm the existence of such photocatalysts and verify the reaction mechanism.
高效利用太阳能在光催化水分解中非常理想。然而,直到现在,太阳光谱的红外部分(构成了太阳能的近一半)尚未被利用,导致太阳能利用效率的显著损失。在这里,我们提出了一种新的水分解机制,其中近红外光可用于产生氢气。这种能力是由于光催化剂独特的电子结构所致,其中价带和导带分布在两个相对的表面上,光催化剂的固有偶极产生了较大的静电位差。这种表面电位差作为光激发电子的辅助助推器,可以有效地降低光催化剂在红外区域分解水所需的带隙。我们对表面功能化六方氮化硼双层的电子结构和光学性质计算证实了这种光催化剂的存在,并验证了反应机制。