DOI: 10.1021/acsami.6c17121 ISSN: 1944-8244

Gas Phase Multizone Synthesis and Localized Deposition of Pt/In Core−Shell Nanoparticles and Their Photothermoelectric Application

Soumya Biswas, Nishchay A Isaac, Syed Hamza Ali Shah, Saptak Majumder, Ahmed Hassan Gohar, Jawahar Rangaraj, Mohammad Saleh Bin Arif, Alper Kaan Soydan, Pedro Henrique de Oliveira Moreira, Arka Mukherjee, Leslie Schlag, Jörg Pezoldt, Heiko O Jacobs

Abstract

Multizone synthesis and localized deposition of bimetallic nanoarchitectures remain major challenges in additive manufacturing at the nanoscale, particularly when control over nanoarchitecture and localized functionality is required. Here, a multizone gas-phase electrodeposition strategy for the simultaneous synthesis and localized deposition of Pt/In core−shell nanoparticles through coupled vapor-phase encapsulation and electrostatic confinement is reported. In contrast to previous gas-phase electrodeposition studies that primarily focused on metallic and metal-oxide nano- and microarchitectures, the present work extends the process to bimetallic core−shell nanoarchitectures as functional nanoscale building blocks. Spark-generated Pt nanoparticles interact in flight with transported In vapor, enabling ligand-free Pt/In encapsulation before deposition. By controlling the In vapor supply through the evaporation temperature, two distinct nanoarchitectures are obtained: centric Pt-core/In-shell nanoparticles (evaporation temperature 750 °C) and eccentric core−shell nanoparticles (evaporation temperature 900 °C) with asymmetric shell distribution. In-flight particle collection reveals that the asymmetry initiates during high-temperature formation and becomes more pronounced during cooling after deposition. The charged Pt/In core−shell nanoparticles are selectively deposited into predefined Si micro-openings and linear patterns. The eccentric Pt/In structures exhibit broadened visible-light absorption and generate a measurable photo-thermoelectric response under illumination at 532 nm. The polarity reversal strongly supports the thermoelectric origin of the response. This approach establishes gas-phase electrodeposition as a route toward localized bimetallic core−shell nanoarchitectures for optothermal and thermoelectric applications.

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