学术文献库

Patterned substrates for optics, electronics, sensing, lab-on-chip technologies, bioanalytics, clinical diagnostics as well as translational and personalized medicine are typically prepared by additive substrate manufacturing including ballistic printing and microcontact printing. However, ballistic printing (e.g., ink jet and aerosol jet printing, laser-induced forward transfer) involves serial pixel-by-pixel ink deposition. Parallel additive pattering by microcontact printing is performed with solid elastomeric stamps suffering from ink depletion after a few stamp-substrate contacts. The throughput limitations of additive state-of-the-art patterning thus arising may be overcome by capillary stamping - parallel additive substrate patterning without ink depletion by mesoporous silica stamps, which enable ink supply through the mesopores anytime during stamping. Thus, either arrays of substrate-bound nanoparticles or colloidal nanodispersions of detached nanoparticles are accessible. We processed three types of model inks: 1) drug solutions, 2) solutions containing metallopolymers and block copolymers as well as 3) nanodiamond suspensions representing colloidal nanoparticle inks. Thus, we obtained aqueous colloidal nanodispersions of stamped drug nanoparticles, regularly arranged ceramic nanoparticles by post-stamping pyrolysis of stamped metallopolymeric precursor nanoparticles and regularly arranged nanodiamond nanoaggregates. Capillary stamping may overcome the throughput limitations of state-of-the-art additive substrate manufacturing while a broad range of different inks can be processed.