Yang Ganceng, Jiao Yanqing, Yan Haijing, Xie Ying, Tian Chungui, Wu Aiping, Wang Yu, Fu Honggang
Key Laboratory of Functional Inorganic Material Chemistry Ministry of Education of the People's Republic of China, Heilongjiang University, Harbin, 150080, China.
Nat Commun. 2022 Jun 6;13(1):3125. doi: 10.1038/s41467-022-30495-1.
Paired electroreduction and electrooxidation of organics with water as a feedstock to produce value-added chemicals is meaningful. A comprehensive understanding of reaction mechanism is critical for the catalyst design and relative area development. Here, we have systematically studied the mechanism of the paired electroreduction and electrooxidation of organics on Fe-Mo-based phosphide heterojunctions. It is shown that active H* species for organic electroreduction originate from water. As for organic electrooxidation, among various oxygen species (OH*, OOH*, and O*), OH* free radicals derived from the first step of water dissociation are identified as active species. Furthermore, explicit reaction pathways and their paired advantages are proposed based on theoretical calculations. The paired electrolyzer powered by a solar cell shows a low voltage of 1.594 V at 100 mA cm, faradaic efficiency of ≥99%, and remarkable cycle stability. This work provides a guide for sustainable synthesis of various value-added chemicals via paired electrocatalysis.
以水为原料对有机物进行成对电还原和电氧化以生产增值化学品具有重要意义。全面了解反应机理对于催化剂设计和相关领域的发展至关重要。在此,我们系统地研究了有机物在铁 - 钼基磷化物异质结上的成对电还原和电氧化机理。结果表明,用于有机电还原的活性H物种源自水。至于有机电氧化,在各种氧物种(OH、OOH和O)中,由水离解第一步产生的OH*自由基被确定为活性物种。此外,基于理论计算提出了明确的反应途径及其成对优势。由太阳能电池供电的成对电解槽在100 mA cm下显示出1.594 V的低电压、≥99%的法拉第效率和出色的循环稳定性。这项工作为通过成对电催化可持续合成各种增值化学品提供了指导。