Yao Yao, Zhu Shangqian, Wang Haijiang, Li Hui, Shao Minhua
Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, China.
Department of Materials Science and Engineering, South University of Science and Technology of China, 1088 Xueyuan Blvd, Nanshan District, Shenzhen, Guangdong, 518055, China.
Angew Chem Int Ed Engl. 2020 Jun 22;59(26):10479-10483. doi: 10.1002/anie.202003071. Epub 2020 Apr 15.
Rh is a promising electrocatalyst for the nitrogen reduction reaction (NRR) given its suitable nitrogen-adsorption energy and low overpotential. However, the NRR pathway on Rh surfaces remains unknown. In this study, we employ surface-enhanced infrared-absorption spectroscopy (SEIRAS) and differential electrochemical mass spectrometry (DEMS) to study the reaction mechanism of NRR on Rh. N H (0≤x≤2) is detected with a N=N stretching mode at ≈2020 cm by SEIRAS and a signal at m/z=29 by DEMS. A new two-step reaction pathway on Rh surfaces is proposed that involves an electrochemical process with a two-electron transfer to form N H and its subsequent decomposition in the electrolyte producing NH . Our results also indicate that nitrate reduction and the NRR share the same reaction intermediate N H .
鉴于其合适的氮吸附能和低过电位,Rh是一种很有前景的用于氮还原反应(NRR)的电催化剂。然而,Rh表面上的NRR途径仍然未知。在本研究中,我们采用表面增强红外吸收光谱(SEIRAS)和差分电化学质谱(DEMS)来研究Rh上NRR的反应机理。通过SEIRAS在≈2020 cm处的N=N伸缩模式以及通过DEMS在m/z=29处的信号检测到了NHx(0≤x≤2)。提出了一种Rh表面上的新的两步反应途径,该途径涉及一个两电子转移的电化学过程以形成NHx及其随后在电解质中分解产生NH3。我们的结果还表明,硝酸盐还原和NRR共享相同的反应中间体NHx。