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April 5, 2026ACS Nanoscience Au0 citationsOpen Access

Removable Nanopore Sealing and In Situ Iron Oxide Nanoparticle Synthesis on Thin Silicon Nitride Membranes

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ZXZehui XiaPBPia BhatiaCMCelia Morral

Key Points

  • The aim is to synthesize iron oxide nanoparticles within silicon nitride nanopores and assess the sealing properties of these pores.
  • In situ synthesis of iron oxide particles was conducted in silicon nitride nanopores through a chemical reaction.
  • Nanopores were created using electroporation, transmission electron microscopy drilling, and hydrofluoric acid etching.
  • Current readout was employed to monitor the chemical synthesis process.
  • Iron oxide nanoparticles were successfully synthesized as mixed magnetite and maghemite.
  • Sealing times for the nanopores varied between approximately 1 ms to 3.6 s depending on size and concentration.
  • The integrity of nanopore arrays was maintained after sealing, cleaning, and recovery.

Abstract

We report in situ synthesis of iron oxide particles inside silicon nitride nanopores via a chemical reaction, monitored by current readout. Nanopores were formed by electroporation on glass chips (diameters from 1.7 to 11.3 nm), transmission electron microscopy (TEM) drilling (diameters from 6.5 to 64.6 nm), or hydrofluoric acid etching (diameters from 12.6 to 36.2 nm) in 5–20 nm thick membranes. Nanopores seal on time scales from ∼1 ms to ∼3.6 s, across a range of sizes and concentrations. We show single and ∼5-pore arrays, as fabricated, after sealing, and after cleaning and pore recovery. These results are independent of the fabrication method. Energy-dispersive X-ray spectroscopy, aberration-corrected scanning TEM, and powder X-ray diffraction verify the synthesis of mixed magnetite and maghemite iron oxide. This work advances nanoparticle–nanopore chips for applications in biosensing, plasmonics, and photonics, where position and size control is required.

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Cite This Study

Xia et al. (2026) studied this question.

synapsesocial.com/papers/69d1fde4a79560c99a0a438chttps://doi.org/10.1021/acsnanoscienceau.6c00032
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