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Sarthak Das

Publications and source records attributed to Sarthak Das.

22 records · Page 2Linked to original sources

Strong Single- and Two-Photon Luminescence Enhancement by Nonradiative Energy Transfer across Layered Heterostructure

The strong light-matter interaction in monolayer transition metal dichalcogenides (TMDs) is promising for nanoscale optoelectronics with their direct band gap nature and the ultra-fast radiative decay of the strongly bound excitons these materials host. However, the impeded amount of light absorption imposed by the ultra-thin nature of the monolayers impairs their viability in photonic applications. Using a layered heterostructure of a monolayer TMD stacked on top of strongly absorbing, non-luminescent, multi-layer SnSe2, we show that both single-photon and two-photon luminescence from the TMD monolayer can be enhanced by a factor of 14 and 7.5, respectively. This is enabled through inter-layer dipole-dipole coupling induced non-radiative Forster resonance energy transfer (FRET) from SnSe2 underneath which acts as a scavenger of the light unabsorbed by the monolayer TMD. The design strategy exploits the near-resonance between the direct energy gap of SnSe2 and the excitonic gap of monolayer TMD, the smallest possible separation between donor and acceptor facilitated by van der Waals heterojunction, and the in-plane orientation of dipoles in these layered materials. The FRET driven uniform single- and twophoton luminescence enhancement over the entire junction area is advantageous over the local enhancement in quantum dot or plasmonic structure integrated 2D layers, and is promising for improving quantum efficiency in imaging, optoelectronic, and photonic applications.

cond-mat.mes-hall↗

Layer degree of freedom for excitons in transition metal dichalcogenides

Layered transition metal dichalcogenides (TMDCs) host a variety of strongly bound exciton complexes that control the optical properties in these materials. Apart from spin and valley, layer index provides an additional degree of freedom in a few-layer thick film. Here we show that in a few-layer TMDC film, the wavefunctions of the conduction and valence band edge states contributing to the K (K') valley are spatially confined in the alternate layers - giving rise to direct (quasi-)intra-layer bright exciton and lower-energy inter-layer dark excitons. Depending on the spin and valley configuration, the bright exciton state is further found to be a coherent superposition of two layer-induced states, one (E-type) distributed in the even layers and the other (O-type) in the odd layers. The intra-layer nature of the bright exciton manifests as a relatively weak dependence of the exciton binding energy on the thickness of the few-layer film, and the binding energy is maintained up to 50 meV in the bulk limit - which is an order of magnitude higher than conventional semiconductors. Fast stokes energy transfer from the intra-layer bright state to the inter-layer dark states provides a clear signature in the layer-dependent broadening of the photoluminescence peak, and plays a key role in the suppression of the photoluminescence intensity observed in TMDCs with thickness beyond monolayer.

cond-mat.mes-hall↗

Inter-layer charge transport controlled by exciton-trion coherent coupling

The possibility of electrical manipulation and detection of charged exciton (trion) before its radiative recombination makes it promising for excitonic devices. Using a few-layer graphene/monolayer WS$_{2}$/monolayer graphene vertical heterojunction, we report inter-layer charge transport from top few-layer graphene to bottom monolayer graphene, mediated by coherently formed trion state. This is achieved by using a resonant excitation and varying the sample temperature, the resulting change in the WS$_{2}$ bandgap allows us to scan the excitation around the exciton-trion spectral overlap with high spectral resolution. By correlating the vertical photocurrent and in situ photoluminescence features at the heterojunction as a function of the spectral position of the excitation, we show that (1) trions are anomalously stable at the junction even up to 463 K due to enhanced doping, and (2) the photocurrent results from the ultra-fast formation of trion through exciton-trion coherent coupling, followed by its fast inter-layer transport. The demonstration of coherent formation, high stabilization, vertical transportation and electrical detection of trions marks a step towards room temperature trionics.

cond-mat.mes-hall↗

Gate tunable WSe2/SnSe2 backward diode with ultrahigh reverse rectification ratio

Backward diodes conduct more efficiently in the reverse bias than in the forward bias, providing superior high frequency response, temperature stability, radiation hardness, and 1/f noise performance than a conventional diode conducting in the forward direction. Here we demonstrate a van der Waals material based backward diode by exploiting the giant staggered band offsets of WSe2/SnSe2 vertical heterojunction. The diode exhibits an ultra-high reverse rectification ratio (R) of ~2.1x10^4 and the same is maintained up to an unusually large bias of 1.5 V - outperforming existing backward diode reports using conventional bulk semiconductors as well as one- and two-dimensional materials by more than an order of magnitude, while maintaining an impressive curvature coefficient (γ) of ~37 per V. The transport mechanism in the diode is shown to be efficiently tunable by external gate and drain bias, as well as by the thickness of the WSe2 layer and the type of metal contacts used. These results pave the way for practical electronic circuit applications using two-dimensional materials and their heterojunctions.

physics.app-ph↗