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首页> 外文期刊>Applied Spectroscopy: Society for Applied Spectroscopy >Digital Signal Processing for Step-Scan Phase and Electrochemical Potential Double-Modulation Fourier Transform Infrared Spectrometry
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Digital Signal Processing for Step-Scan Phase and Electrochemical Potential Double-Modulation Fourier Transform Infrared Spectrometry

机译:步进扫描相位和电化学势双调制傅立叶变换红外光谱的数字信号处理

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摘要

Step-scan double-modulation (phase and electrochemical potential) Fourier transform infrared (FT-IR) spectrometry provides both spectroscopic and dynamic information about faradaic reactions. Recently introduced digital signal processing (DSP) can be used, instead of two lock-in amplifiers, for the optical signal demodulation at two modulation frequencies. In order to establish the merits of double-modulation FT-IR spectrometry with DSP, spectro-electrochemical experiments are performed in the attenuated total reflection configuration and with the commonly used ferri/ferrocyanide redox couple. Because of a large potential drop associated with the uncompensated resistance, a satisfactory signal-to-noise ratio for the alternating current (ac) optical measurements is obtained only with the employment of positive feedback compensation. In this arrangement, the amplitude of electrochemical modulation is sufficiently large to convert a significant fraction of the reduced form to the oxidized form and back to the reduced form. Large amplitude ac voltammetry demonstrates that the phase of faradaic admittance at the formal potential is approximately 45° at 2.00 Hz. In addition, these experiments allow for calculation of the interfacial ac potential. This variable is needed for the normalization of the in-phase and the quadrature spectra in order to overcome the problem associated with the iR_(u) drop. Because of the integral relationship between the faradaic current and the electromodulation reflectance coefficient, the phases of electromodulation reflectance coefficient with respect to the interfacial ac potential are expected to be -45° and 135° for the reduced and oxidized forms, respectively. However, dynamic information from double-modulation FT-IR spectrometry is available only if demodulation at the electrochemical potential modulation frequency is performed with respect to a defined phase. Because of an undefined demodulation phase implemented in the current version of DSP software, step-scan double-modulation FT-IR spectrometry with DSP is suitable only to provide spectroscopic information. In order to overcome this limitation, the demodulation of the ac optical signal at the electrochemical modulation frequency must be synchronized in phase with the ac potential modulation applied to the electrochemical cell.
机译:步进扫描双调制(相位和电化学势)傅里叶变换红外(FT-IR)光谱提供有关法拉第反应的光谱和动态信息。可以使用最近推出的数字信号处理(DSP)代替两个锁定放大器,以两个调制频率进行光信号解调。为了确定使用DSP进行双调制FT-IR光谱分析的优点,在衰减的全反射配置下以及常用的三价铁/亚铁氰化物氧化还原对进行了光谱电化学实验。由于与未补偿电阻相关的大电位降,仅通过使用正反馈补偿,即可获得用于交流电(ac)光学测量的令人满意的信噪比。在这种布置中,电化学调制的幅度足够大,以将很大一部分还原形式转化为氧化形式并返回还原形式。大振幅交流伏安法表明法拉第导纳在形式电势下的相位在2.00 Hz时约为45°。另外,这些实验允许计算界面交流电势。为了克服同相和正交光谱的标准化,需要使用此变量,以克服与iR_(u)下降相关的问题。由于法拉第电流与电调制反射系数之间的积分关系,对于还原和氧化形式,相对于界面交流电势,电调制反射系数的相位分别预计为-45°和135°。但是,只有在相对于定义的相位以电化学电势调制频率进行解调的情况下,才能获得来自双调制FT-IR光谱的动态信息。由于在当前版本的DSP软件中实现了未定义的解调阶段,因此使用DSP进行步进扫描双调制FT-IR光谱仅适用于提供光谱信息。为了克服该限制,必须将在电化学调制频率下的交流光信号的解调与施加到电化学电池的交流电势调制同相同步。

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