4.8 Article

What Determines the Electrochemical Properties of Nitrogenated Amorphous Carbon Thin Films?

期刊

CHEMISTRY OF MATERIALS
卷 33, 期 17, 页码 6813-6824

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.1c01519

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资金

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC0276SF00515]
  2. Walter Ahlstrom Foundation
  3. European Union [841621]
  4. Business Finland [FEPOD 2117731]
  5. Academy of Finland [30488]
  6. Marie Curie Actions (MSCA) [841621] Funding Source: Marie Curie Actions (MSCA)

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The experimental investigation enhanced by computational analyses reveals the significant impact of nitrogen doping on the structure and electrochemical performance of carbon films, including disruption of the C-C structure, increased surface roughness, and enhanced conductivity. These changes are associated with the increase in hydrogen and oxygen content in the films due to nitrogen doping.
Linking structural and compositional features with the observed electrochemical performance is often ambiguous and sensitive to known and unknown impurities. Here an extensive experimental investigation augmented by computational analyses is linked to the electrochemical characterization of in situ nitrogen-doped tetrahedral amorphous carbon thin films (ta-C:N). Raman spectroscopy combined with X-ray reflectivity shows nitrogen disrupting the sp(3) C-C structure of the reference ta-C, supported by the observations of graphitic nitrogen substitution in X-ray absorption spectroscopy. The surface roughness also increases, as observed in atomic force microscopy and atomic-level computational analyses. These changes are linked to significant increases in the hydrogen and oxygen content of the films by utilizing time-of-flight elastic recoil detection analysis. The conductivity of the films increases as a function of the nitrogen content, which is seen as a facile reversible outer-sphere redox reaction on ta-C:N electrodes. However, for the surface-sensitive inner-sphere redox (ISR) analytes, it is shown that the electrochemical response instead follows the oxygen and hydrogen content. We argue that the passivation of the required surface adsorption sites by hydrogen decreases the rates of all of the chemically different ISR probes investigated on nitrogenated surfaces significantly below that of the nitrogen-free reference sample. This hypothesis can be used to readily rationalize many of the contradictory electrochemical results reported in the literature.

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