Surface-Plasmon-Driven Solution-Phase Growth of Germanium Nanostructures on Lithographically Defined Nanogap Antenna Arrays

View at publisher
Authors: Rachel O’Meara, B. R. Tak, Kamonpan Chumpol, N. Alattar, R. G. Hobbs
Cited by: 1
References: 71

Abstract

Low-temperature, spatially selective fabrication of semiconductor nanostructures is essential for next-generation microelectronics, where back-end-of-line (BEOL) thermal budgets limit conventional high-temperature processing. Here, we demonstrate a plasmon-driven, solution-phase route to site-controlled growth of both crystalline and amorphous germanium nanostructures using lithographically defined Au nanoantennas and a diphenylgermane precursor. Resonant excitation at 785 nm of localized surface plasmon resonances (LSPRs) in Au nanogap antenna arrays can generate intense near-field photothermal heating, driving precursor decomposition and Ge nanostructure growth while avoiding global heating of the growth substrate. In this work, we demonstrate plasmon-driven growth of crystalline Ge nanowires at locations determined by lithographically defined Au nanoantennas. Nanowire growth is demonstrated on both bulk ITO/glass substrates and ultrathin 10 nm-thick SiN x membranes to support characterization by transmission electron microscopy. The thermal conductivity of the substrates was found to dictate the optical power threshold required for catalytic nanowire growth. High-resolution TEM confirms the growth of single-crystalline Ge nanowires, while Raman spectroscopy also confirms the growth of Ge nanostructures. This approach may provide a low-thermal budget pathway for production of Ge photodetectors or other nanoelectronic devices directly onto BEOL metallization layers.

Fields of Study & Subjects

Nanowire Synthesis and Applications Thermal properties of materials Mechanical and Optical Resonators

Publication details

Journal / source
The Journal of Physical Chemistry C
Publisher
American Chemical Society (ACS)
Volume
130
Issue
4
Pages
1572–1581
Publication date
13 January 2026
Language
EN