Haq Tanveer Ul, Haik Yousef
Sustainable Energy Engineering Frank H. Dotterweich College of Engineering Texas A&M University Kingsville TX 78363-8202 USA.
Department of Mechanical and Nuclear Engineering University of Sharjah Sharjah UAE.
Small Sci. 2022 Aug 16;2(9):2200030. doi: 10.1002/smsc.202200030. eCollection 2022 Sep.
Compared with freshwater splitting, seawater electrolysis has more spaces to be explored, which is primarily attributed to the additional critical catalytic challenges of the competition between anodic oxygen evolution reaction (OER) and chlorine chemistry, deep corrosion, and site blocking due to the presence of chloride ions and insoluble particulate in seawater. However, if direct seawater electrolysis can be realized, it would revolutionize the energy and environmental sectors. In this review, the current effective strategies are summarized, including electronic modulation, oxygen vacancies creation, amorphous and porous structure design, corrosion-resistant passive layer decoration, and creating strong catalyst-support interactions. The review also provides insights for seawater electrolysis on rational design of the OER catalyst with high selectivity, activity, corrosion resistance, chemical, and mechanical durability. Beyond the progress made to date, a perspective in the fabrication of high-performance anodes for direct seawater electrolysis is also proposed. Collectively, this review will shed light on the rational design of a viable anode for massive and sustainable hydrogen fuel production from immense seawater.
与淡水分解相比,海水电解有更多有待探索的空间,这主要归因于阳极析氧反应(OER)与氯化学之间的竞争、深度腐蚀以及由于海水中存在氯离子和不溶性颗粒而导致的位点阻塞等额外的关键催化挑战。然而,如果能够实现直接海水电解,将会给能源和环境领域带来变革。在这篇综述中,总结了当前有效的策略,包括电子调制、氧空位的产生、非晶态和多孔结构设计、耐腐蚀钝化层修饰以及建立强大的催化剂-载体相互作用。该综述还为海水电解在合理设计具有高选择性、活性、耐腐蚀性、化学和机械耐久性的OER催化剂方面提供了见解。除了迄今取得的进展外,还提出了关于直接海水电解高性能阳极制造的展望。总的来说,这篇综述将为从大量海水中大规模可持续生产氢燃料的可行阳极的合理设计提供启示。