Wang Mengfan, Liu Sisi, Ji Haoqing, Yang Tingzhou, Qian Tao, Yan Chenglin
College of Energy, Key Laboratory of Advanced Carbon Materials and Wearable Energy Technologies of Jiangsu Province, Soochow University, Suzhou, China.
School of Chemistry and Chemical Engineering, Nantong University, Nantong, China.
Nat Commun. 2021 May 27;12(1):3198. doi: 10.1038/s41467-021-23360-0.
The electroreduction of nitrogen to ammonia offers a promising alternative to the energy-intensive Haber-Bosch process. Unfortunately, the reaction suffers from low activity and selectivity, owing to competing hydrogen evolution and the poor accessibility of nitrogen to the electrocatalyst. Here, we report that deliberately triggering a salting-out effect in a highly concentrated electrolyte can simultaneously tackle the above challenges and achieve highly efficient ammonia synthesis. The solute ions exhibit strong affinity for the surrounding HO molecules, forming a hydration shell and limiting their efficacy as both proton sources and solvents. This not only effectively suppresses hydrogen evolution but also ensures considerable nitrogen flux at the reaction interface via heterogeneous nucleation of the precipitate, thus facilitating the subsequent reduction process in terms of both selectivity and activity. As expected, even when assembled with a metal-free electrocatalyst, a high Faradaic efficiency of 71 ± 1.9% is achieved with this proof-of-concept system.
将氮气电还原为氨为能源密集型的哈伯-博施法提供了一种有前景的替代方案。不幸的是,由于竞争性析氢以及氮气与电催化剂的接触性较差,该反应存在活性和选择性较低的问题。在此,我们报告称,在高浓度电解质中刻意引发盐析效应可同时应对上述挑战并实现高效氨合成。溶质离子对周围的水分子表现出很强的亲和力,形成水合壳层并限制了它们作为质子源和溶剂的功效。这不仅有效抑制了析氢,还通过沉淀物的异相成核确保了反应界面处可观的氮通量,从而在选择性和活性方面促进了后续的还原过程。不出所料,即使与无金属电催化剂组装在一起,该概念验证系统也实现了71±1.9%的高法拉第效率。