u表面电化学氮还原的谱学研究
采用衰减全反射表面增强红外吸收光谱(ATR-SEIRAS)与差分电化学质谱(DEMS)技术,对Au电极表面电化学氮还原反应(NRR)过程进行实时动态监测。实验结果表明:在N2饱和的电解质溶液中,红外光谱图出现了位于2958 cm-1(N-H伸缩振动)、1480 cm-1(H-N-H弯曲振动)、1330 cm-1(-NH2对称振动)及1110 cm-1(N-N伸缩振动)等关键中间物种的特征吸收峰,并结合Ar气氛对照实验证实了上述含氮物种确系氮气还原的产物。通过差分电化学质谱检测到了m/z=31(NH-NH2)的生成信号,这一发现为Au电极表面氮气还原遵循缔合交替机制提供了直接实验证据。该研究通过电化学原位光谱与质谱技术的协同分析,成功实现了对氮还原反应机制的动态解析。
ttenuated total reflection surface-enhanced infrared absorption spectroscopy (ATR-SEIRAS) and differential electrochemical mass spectrometry (DEMS) were used for in situ monitoring the electrochemical nitrogen reduction reaction (NRR) process on Au electrode.The results showed that in N2-saturated electrolyte solution, the characteristic absorption peaks ofkey intermediate species located at 2958 cm-1 (N-H stretching vibration), 1480 cm-1 (H-N-H bending vibration), 1330 cm-1 (-NH2 symmetrical vibration), and 1110 cm-1 (N-N stretching vibration), and the nitrogen-containing species were confirmed to bethe products of nitrogen reductionin combination with Ar atmosphere control experiments.The signal of m/z=31 (NH-NH2) was detected by differential electrochemical mass spectrometry, this finding provides the direct experimental evidence that nitrogen reduction on Au electrode follows an associative alternationmechanism. This study has successfully realized the dynamic analysis of the NRR mechanism by combining the electrochemical in situ spectroscopy and mass spectrometry techniques.
刘庆飞、谭伟玲、涂云川
重庆大学化学化工学院,重庆,401331重庆大学化学化工学院,重庆,401331重庆大学化学化工学院,重庆,401331
化学自然科学研究方法
原位表征技术红外吸收光谱差分电化学质谱电化学氮还原反应机制?
In situ characterization techniquesinfrared absorption spectrumDEMSeNRRreaction mechanisms
刘庆飞,谭伟玲,涂云川.u表面电化学氮还原的谱学研究[EB/OL].(2025-04-15)[2025-05-01].http://www.paper.edu.cn/releasepaper/content/202504-127.点此复制
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