Paul Berger

25 April 2013

What are your main research interests?

My work focuses upon active semiconductor devices, often exploring ways to use new materials or modify material’s properties to create enhanced device performance. Over the years my work has studied every major semiconductor device, including HBT, MODFET, tunnel diodes, LEDs, laser diodes, solar cells, photodetectors, and optical modulators. Currently, our group explores both inorganic and organic semiconductors and spans the gamut from Si/SiGe to III-V’s, polythiophene etc. and graphene.  The most reoccurring theme is quantum tunnelling based devices which is represented in three funded programs and covers three distinct semiconductor material systems (SiGe, III-nitrides and polymers).

What has motivated you to research in vivo protein biosensors?

Open discussions with a colleague in the biomedical engineering discipline peaked my curiosity, which excited me to their specific need and the opportunity I could exploit by judicious engineering. Their team was developing a nitride-based sensor, but its cost and yield clearly was going to temper their long-term impact. They had even shown in preliminary experiments that Si-based sensors drifted too much to be usable. That triggered me to examine why the silicon sensor drifted and how we could improve upon that and test it in a facile manner. The biocapacitors described in our Letter are a result of a streamlined analytical analysis of this ion percolation into the sensor.

Can you explain the advance that you have reported in your Electronics Letters paper?

Essentially, the usage of a generic in vivo silicon based sensor will drift with its threshold voltage constantly moving as alkali ions (i.e. Na and K) intercalate into the standard silicon dioxide gate oxide. Here we report on a drift-free bio-capacitor that can be the platform for drift-free biosensors. The substitution of silicon dioxide with aluminium oxide deposited by atomic layer deposition already shows extreme promise in blocking ion penetration. Our exploration of other alternatives is just commencing.

Which particular applications could benefit most from this result?

In working with various teams within our medical school, we aim to facilitate the detection of organ transplant rejection before it is too late, allowing proper dosing of patients with anti-rejection medicines, as well as laying a foundation for developing artificial neurons. In essence, there are many implanted electronics, such as pace makers, but these are always encapsulated and the electronics is never in direct contact with bodily fluids. Advances, such as this, could open the door to electronics interacting directly with the human body, both sensing and stimulating.

What are you doing to continue and build on this work?

Next we are building the biosensor for targeted protein recognition.

What other related projects  is your group working on?

We are also exploring plasmonically assisted plastic solar cells for energy harvesting. These plastic solar cells could be almost ‘painted’ atop any curved surface and allow greater penetration of photovoltaics into society as point-of-use power generation.

How do you see in vivo biosensing technology progressing over the next few years?

We aim to demonstrate a facile approach for in vivo protein sensing that could be decorated along the shaft of a diagnostic needle and used to measure and map transplanted organ health in real-time, as readily as an expectant mother has amniocentesis (also referred to as amniotic fluid test or AFT) testing. We aim to embark upon a further materials study of the gate oxide alternatives and take the best performers in the biocapacitor platform and translate that to working biosensors that can be pre-qualified.

Further reading

A PDF version (new window) of this interview is available.

Journal content

Cover of Electronics Letters, Volume 49, Issue 25

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Browse or search all papers in the latest or past issues of Electronics Letters on the IET Digital Library.