Characterizing Density and Spatial Distribution of Trap States in TaN Thin Films for Rational Defect Passivation.

ACS Appl Mater Interfaces

Department of Applied Physical Sciences, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

Published: February 2023

AI Article Synopsis

  • * A study utilizing drive-level capacitance profiling (DLCP) identifies a high density of deep trap states at the interfaces of TaN thin films, significantly affecting their properties and function.
  • * A new passivation strategy involving silatrane moieties has been developed, which reduces the defect density at the surface and the free carrier density, enhancing the efficiency of TaN films by minimizing recombination of photoexcited carriers.

Article Abstract

Tantalum nitride (TaN) has gained significant attention as a potential photoanode material, yet it has been challenged by material quality issues. Defect-induced trap states are detrimental to the performance of any semiconductor material. Beyond influencing the performance of TaN films, defects can also accelerate the degradation in water during desired electrochemical applications. Defect passivation has provided an enormous boost to the development of many semiconductor materials but is currently in its infancy for TaN. This is in part due to a lack of experimental understanding regarding the spatial and energetic distribution of trap states throughout TaN thin films. Here, we employ drive-level capacitance profiling (DLCP) to experimentally resolve the spatial and energetic distribution of trap states throughout TaN thin films. The density of deeper energetic traps is found to reach ∼2.5 to 6 × 10 cm at the interfaces of neat TaN thin films, over an order of magnitude greater than the bulk. In addition to the spatial profile of deep trap states, we report neat TaN thin films to be highly n-type in nature, owning a free carrier density of ∼9.74 × 10 cm. This information, coupled with the present understanding of native oxide layers on TaN, has facilitated the rational design of a targeted passivation strategy that simultaneously provides a means for catalyst immobilization. Loading catalyst via silatrane moieties suppresses the density of defects at the surface of TaN thin films by two orders of magnitude, while also reducing the free carrier density of films by over one order of magnitude, effectively dedoping the films to ∼2.40 × 10 cm. The surface passivation of TaN films translates to suppressed defect-induced trapping and recombination of photoexcited carriers, as determined through absorption, photoluminescence, and transient photovoltage. This illustrates how developing a deeper understanding of the distribution and influence of defects in TaN thin films has the potential to guide future works and ultimately accelerate the integration and development of high-performance TaN thin film devices.

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http://dx.doi.org/10.1021/acsami.2c19275DOI Listing

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