Xiao Yuhang, Tan Xiaohong, Du Binjie, Guo Yingying, He Weidong, Cui Hao, Wang Chengxin
School of Materials Science and Engineering, Sun Yat-sen University, Guangzhou, 510275, China.
Angew Chem Int Ed Engl. 2024 Sep 2;63(36):e202408758. doi: 10.1002/anie.202408758. Epub 2024 Aug 2.
Electrochemical nitrate reduction reaction (NitRR) uses nitrate from wastewater, offering a hopeful solution for environmental issues and ammonia production. Yet, varying nitrate levels in real wastewater greatly affect NitRR, slowing down its multi-step process. Herein, a multi-strategy approach was explored through the design of ordered mesoporous intermetallic AuCu nanocorals with ultrathin Au skin (meso-i-AuCu@ultra-Au) as an efficient and concentration-versatile catalyst for NitRR. The highly penetrated structure, coupled with the compressive stress exerted on the skin layer, not only facilitates rapid electron/mass transfer, but also effectively modulates the surface electronic structure, addressing the concentration-dependent challenges encountered in practical NitRR process. As expected, the novel catalyst demonstrates outstanding NitRR activities and Faradaic efficiencies exceeding 95 % across a real and widespread concentration range (10-2000 mM). Notably, its performance at each concentration matched or exceeded that of the best-known catalyst designed for that concentration. Multiple operando spectroscopies unveiled the catalyst concurrently optimized the adsorption behavior of different intermediates (adsorbed *NO and *H) while expediting the hydrogenation steps, leading to an efficient overall reduction process. Moreover, the catalyst also displays promising potential for use in ammonia production at industrial-relevant current densities and in conceptual zinc-nitrate batteries, serving trifunctional nitrate conversion, ammonia synthesis and power supply.
电化学硝酸盐还原反应(NitRR)利用废水中的硝酸盐,为环境问题和氨生产提供了一个有希望的解决方案。然而,实际废水中不同的硝酸盐水平极大地影响了NitRR,减缓了其多步过程。在此,通过设计具有超薄金壳的有序介孔金属间化合物AuCu纳米珊瑚(介孔-i-AuCu@ultra-Au)作为一种高效且浓度适应性强的NitRR催化剂,探索了一种多策略方法。高度渗透的结构,加上施加在壳层上的压应力,不仅促进了快速的电子/质量传递,还有效地调节了表面电子结构,解决了实际NitRR过程中遇到的浓度依赖性挑战。正如预期的那样,这种新型催化剂在实际且广泛的浓度范围(10 - 2000 mM)内表现出出色的NitRR活性和超过95%的法拉第效率。值得注意的是,它在每个浓度下的性能都与或超过了为该浓度设计的最知名催化剂。多种原位光谱揭示,该催化剂在加快氢化步骤的同时,还能同时优化不同中间体(吸附的NO和H)的吸附行为,从而实现高效的整体还原过程。此外,该催化剂在与工业相关的电流密度下用于氨生产以及在概念性硝酸锌电池中也显示出有前景的潜力,可实现三功能硝酸盐转化、氨合成和供电。