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Biomedical subjects

Philippe Buhlmann

Publications and source records attributed to Philippe Buhlmann.

2 recordsLinked to original sources

Sequential shape-and-solder-directed self-assembly of functional microsystems.

We demonstrate the fabrication of packaged microsystems that contain active semiconductor devices and passive components by using a directed self-assembly technique. The directed self-assembly is accomplished by combining geometrical shape recognition with site-specific binding involving liquid solder. Microfabricated components with matching complementary shapes, circuits, and liquid solder-coated areas were suspended in ethylene glycol and agitated by using a turbulent liquid flow to initiate the self-assembly. Microsystems were obtained by sequentially adding components of different types. Six hundred AlGaInP/GaAs light-emitting diode segments with a chip size of 200 microm were assembled onto device carriers with a yield of 100% in 2 min. Packaged light-emitting diodes formed with yields exceeding 97% as a result of two self-assembly steps in 4 min. This self-assembly procedure, based on geometrical shape recognition and subsequent binding to form mechanical and electrical connections, provides a high distinguishing power between different components and a route to nonrobotic parallel assembly of electrically functional hybrid microsystems in three dimensions.

Computers↗

Scanning tunneling microscopy with chemically modified gold tips: in situ reestablishment of chemical contrast.

A method was developed for the reestablishment of chemical contrast in STM images obtained with chemically modified gold tips. Such tips display selective chemical contrast, which allows the selective imaging of specific species on the sample surface. Chemically modified STM tips can be fabricated by forming a self-assembled monolayer (SAM) on an electrochemically etched gold tip. One difficulty with this method thus far has been the relatively short lifetime of SAM-treated tips. The method described here utilizes the brief application of a high bias voltage between the sample and the tip to cause SAM molecules to reoccupy the tip apex, thereby allowing the tips to display selective chemical contrast in imaging. These treatments consist of applying a +1.9-V sample bias for 0.5-10 min under tunneling conditions. The usable lifetime of SAM-modified tips could be increased by more than 2 orders of magnitude, from hours to at least a month, dramatically increasing the efficiency of using SAM-modified gold tips. SAM molecules can also be removed from the tip apex by application of a negative sample bias (-2.0 V for 0.5-10 min) making it possible to alternate between conventional STM images and STM images with chemically enhanced contrasts.

Journal Article↗