Xie Jianhui, Yang Tingting, Hong Longzhu, Li Hui, Li Bing, Guo Zhenguo, Liu Yingying, Lau Tai-Chu
Anhui Province Key Laboratory of Advanced Catalytic Materials and Reaction Engineering, School of Chemistry and Chemical Engineering, Hefei University of Technology, Hefei 230009, P. R. China.
Institute of Intelligent Machines, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei 230031, P. R. China.
J Am Chem Soc. 2025 Apr 30;147(17):14211-14218. doi: 10.1021/jacs.4c16902. Epub 2025 Apr 17.
The electrocatalytic oxidation of ammonia using molecular catalysts has attracted much attention recently due to its potential for fuel cell applications. In this study, we report the electrocatalytic ammonia oxidation (AO) by [Ru(salchda)(NH)(CHCN)] (, salchda = '-bis(salicylidene)--cyclohexyldiamine dianion) and its bromo derivative. Controlled potential electrolysis at 0.65 V versus Fc for 3.2 h of a solution of and NH in CHCN produced N with a TON of 26 and Faradaic efficiency (FE) close to 100%. The TON was increased to 79 and 147 when electrolysis was carried out at 0.7 and 0.80 V vs Fc, respectively, with FE maintained at >99%, which are the highest among molecular ruthenium catalysts. An active intermediate was detected and shown to be the corresponding ruthenium(VI) nitrido complex [Ru(salchda)(N)] () by direct comparison with an authentic sample of , which we have previously synthesized and fully characterized. Direct kinetic studies on the oxidation of NH to N have also been carried out and the results are consistent with parallel electrophilic attack of NH by and bimolecular N···N coupling of to produce N. DFT calculations have also been performed to support the proposed mechanism.
近年来,利用分子催化剂对氨进行电催化氧化因其在燃料电池应用中的潜力而备受关注。在本研究中,我们报道了[Ru(salchda)(NH)(CHCN)](salchda = '-双(水杨醛)-环己二胺二价阴离子)及其溴代衍生物对氨的电催化氧化(AO)。在相对于Fc为0.65 V的条件下,对 和NH在CHCN中的溶液进行3.2 h的控制电位电解,生成N,TON为26,法拉第效率(FE)接近100%。当分别在相对于Fc为0.7和0.80 V的条件下进行电解时,TON分别提高到79和147,FE保持在>99%,这是分子钌催化剂中最高的。检测到一种活性中间体,并通过与我们之前合成并完全表征的 的真实样品直接比较,证明其为相应的钌(VI)氮化物配合物[Ru(salchda)(N)]()。还对NH氧化为N进行了直接动力学研究,结果与 通过亲电进攻NH以及 进行双分子N···N偶联生成N的平行反应一致。还进行了DFT计算以支持所提出的机理。