Kang Yuyang, Chen Runze, Zhen Chao, Wang Lianzhou, Liu Gang, Cheng Hui-Ming
Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China; School of Materials Science and Engineering, University of Science and Technology of China, Shenyang 110016, China.
Shenyang National Laboratory for Materials Science, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China; Key Laboratory for Anisotropy and Texture of Materials (Ministry of Education), Northeastern University, Shenyang 110819, China.
Sci Bull (Beijing). 2020 Jul 30;65(14):1163-1169. doi: 10.1016/j.scib.2020.03.041. Epub 2020 Mar 30.
Common solar-driven photoelectrochemical (PEC) cells for water splitting were designed by using semiconducting photoactive materials as working photoelectrodes to capture sunlight. Due to the thermodynamic requirement of 1.23 eV and kinetic energy loss of about 0.6 eV, a photo-voltage of 1.8 V produced by PEC cells is generally required for spontaneous water splitting. Therefore, the minimum bandgap of 1.8 eV is demanded for photoactive materials in single-photoelectrode PEC cells, and the bandgap of about 1 eV for back photoactive materials is appropriate in tandem PEC cells. All these PEC cells cannot effectively utilize the infrared light from 1250 to 2500 nm. In order to realize the full spectrum utilization of solar light, here, we develop a solar-driven PEC water splitting system integrated with a thermoelectric device. The key feature of this system is that the thermoelectric device produces a voltage as an additional bias for the PEC system by using the temperature difference between the incident infrared-light heated aqueous electrolyte in the PEC cell as the hot source and unirradiated external water as the cold source. Compared to a reference PEC system without the thermoelectric device, this system has a significantly improved overall water splitting activity of 1.6 times and may provide a strategy for accelerating the application of full spectrum solar light-driven PEC cells for hydrogen production.
常见的用于水分解的太阳能驱动光电化学(PEC)电池是通过使用半导体光活性材料作为工作光电极来捕获太阳光而设计的。由于水分解需要1.23电子伏特的热力学能以及约0.6电子伏特的动能损失,因此PEC电池产生1.8伏的光电压通常是自发水分解所必需的。因此,单光电极PEC电池中的光活性材料需要至少1.8电子伏特的带隙,而在串联PEC电池中,背侧光活性材料约1电子伏特的带隙是合适的。所有这些PEC电池都不能有效地利用1250至2500纳米的红外光。为了实现太阳光的全光谱利用,在此我们开发了一种与热电装置集成的太阳能驱动PEC水分解系统。该系统的关键特性是,热电装置利用PEC电池中入射红外光加热的水性电解质作为热源与未受照射的外部水作为冷源之间的温差产生电压,作为PEC系统的额外偏压。与没有热电装置的参考PEC系统相比,该系统的整体水分解活性显著提高了1.6倍,并且可能为加速全光谱太阳能驱动PEC电池用于制氢的应用提供一种策略。