Transition-metal
dichalcogenides (TMDs), including molybdenum disulfide
(MoS2) and tungsten disulfide (WS2), with appealing
properties have recently become promising alternatives to graphene
with semimetal and low on/off current ratio properties as the sensing
channel in field-effect transistor (FET) biosensors. However, the
efficiency of DNA-based FET devices strongly depends on how DNA probes
are tethered to the nanomaterial channels. As against covalent attachment,
simple DNA physisorption has become increasingly popular, and a DNA
sequence with strong affinity for nanomaterials is still highly sought
after. Recently, poly-cytosine (poly-C) DNA was found to be strongly
adsorbed to many common nanomaterials, including WS2. Herein,
a diblock DNA probe containing a (poly-C) (C15) was used to attach
to a chemical vapor deposition (CVD)-grown monolayer WS2 surface; meanwhile, the target complementary DNA (cDNA) was hybridized
to the other block of the DNA probe. The biosensor developed following
this strategy led to a limit of detection down to 3 aM within a concentration
range spanning over approximately 7 orders of magnitude (10–16 to 10–9 M), which was lower than those of the
previously reported TMDs and a good competitor to graphene FET DNA
biosensors. Moreover, the proposed WS2 FET DNA biosensor
showed high specificity capable of distinguishing the cDNA from non-cDNA,
one-base mismatched DNA, two-base mismatched DNA, and three-base mismatched
DNA, making our strategy an exciting avenue for disease diagnosis.
The authors are convinced that this work extends the CVD synthesis
of WS2 and its promise in biosensing application-based
FETs.