Doping and Dedoping Processes of Polypyrrole: DFT Study with Hybrid Functionals

作者：Ullah Habib; Shah Anwar ul Haq Ali^*; Bilal Salma; Ayub Khurshid

来源：Journal of Physical Chemistry C, 2014, 118(31): 17819-17830.

DOI：10.1021/jp505626d

Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations at the UB3LYP/6-31G(d) level have been performed to investigate the tunable nature, i.e., doping and dedoping processes, of polypyrrole (PPy). The calculated theoretical data show strong correlation with the recent experimental reports, which validates our computational protocol. The calculated properties are extrapolated to the polymer (PPy) through a second-order polynomial fit. Changes in band gap, conductivity, and resistance of nPy and nPy-X (where n = 1-9 and X = +, NH3, and Cl) were studied and correlated with the calculated vibrational spectra (IR) and electronic properties. Upon doping, bridging bond distance and internal bond angles decrease (decrease in resistance over polymer backbone), whereas dedoping results in increases in these geometric parameters. In the vibrational spectrum, doping is characterized by an increase in the band peaks in the fingerprint region and/or red shifting of the spectral bands. Dedoping (9Py(+) with NH3), on the other hand, results in decreases in the number of vibrational spectral bands. In the UV vis and UV-vis-near-IR spectra, the addition of different analytes (dopant) to 9Py results in the disappearance of certain bands and gives rise to some new absorbances corresponding to localized and delocalized polaron bands. Specifically, the peaks in the near-IR region at 1907 nm for Py+ and 1242 nm for 9Py-Cl are due to delocalized and localized polaron structures, respectively. Upon p-doping, the band gaps and resistance of nPy decrease, while its conductivity and pi-electron density of conjugation increase over the polymeric backbone. However, a reversal of properties is obtained in n-doping or reduction of nPy(+). In the case of oxidation and Cl dopant, the IP and EA increase, and consequently, there is a decrease in the band gap. NBO and Mulliken charges analyses indicate charge transferring from the polymer in the case of p-type dopants, while this phenomenon is reversed with n-type dopants.

• 出版日期2014-8-7