Investigating charge transport in a <i>p</i>-Si/<i>n</i>-poly(benzimidazobenzophenanthroline)-BBL thin film heterojunction diode
The physics of charge transport across the interface in an inorganic Si/organic conducting polymer junction diode has received little attention compared to the inorganic<i>p-n</i>silicon diode. One reason is the amorphous nature of the organic polymer and the polymer chain orientation which introduces disorder and barriers to charge flow. Herein we first present an easy technique to fabricate an inorganic/organic,<i>p</i>-Si/<i>n</i>-poly(benzimidazobenzophenanthroline-BBL) junction diode. The physics of charge transport across the heterojunction, and in the BBL film is then analyzed from the device current-voltage characteristics as a function of temperature in the range 150 K <<i>T</i>< 370 K. The temperature dependence of the diode ideality parameter and of the saturation current density demonstrate that tunneling enhanced charge recombination via exponential trap distributions in the depletion region was responsible for charge transport across the junction. Furthermore, the temperature dependence of the diode conductance revealed that thermal activation and hopping both contributed to charge transport in the BBL film away from the junction. BBL is a ladder polymer with a discrete layered crystal structure that is oriented perpendicular to the substrate. Such polymer chain orientation, combined with a distribution of bond lengths and numerous conjugation paths available for charge delocalization result in the multiple charge transport mechanisms as observed in the diode.
Authors
- Nicholas J. Pinto (ORCID: https://orcid.org/0000-0003-0954-6539)
- Alejandro J. Cruz‐Arzon
Institutions
- University of Puerto Rico at Humacao (PR)
Publication Details
- Journal
- Journal of Physics Condensed Matter
- Published
- 2025-04-16
- DOI
- https://doi.org/10.1088/1361-648x/adcdb0
- Primary Topic
- Semiconductor materials and interfaces
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Science Foundation