Photovoltaic Characteristics of GaSe/MoSe2 Heterojunction Devices.

The two-dimensional materials have the thickness of an atomic layer level and are expected as alternative materials for future electronics and optoelectronics due to their specific properties. Especially recently, transition metal monochalcogenides and dichalcogenides have attracted attention. Since these materials have a band gap unlike graphene and exhibit a semiconductor property even in a single layer, application to a new flexible optoelectronics is expected. In this study, the photovoltaic characteristics of a GaSe/MoSe2 heterojunction device using two-dimensional semiconductors, p-type GaSe and n-type MoSe2, were investigated. The heterojunction device was prepared by transferring GaSe and MoSe2 onto the substrate which the titanium electrodes were fabricated through a mechanical peeling method. The current-voltage characteristics of the GaSe/MoSe2 heterojunction device were measured in a dark condition and under light irradiation using a solar simulator. The irradiation light intensity was changed from 0.5 to 1.5 sun. It was found that when the illuminance was increased in this illuminance range, both the short-circuit current and the open-circuit voltage increased. The open-circuit voltage and the energy conversion efficiency were 0.41 V and 0.46% under 1.5 sun condition, respectively.

The effect of gold quantum dots/grating-coupled surface plasmons in inverted organic solar cells.

We studied the effect of gold quantum dots (AuQDs)/grating-coupled surface plasmon resonance (GC-SPR) in inverted organic solar cells (OSCs). AuQDs are located within a GC-SPR evanescent field in inverted OSCs, indicating an interaction between GC-SPR and AuQDs' quantum effects, subsequently giving rise to improvement in the performance of inverted OSCs. The fabricated solar cell device comprises an ITO/TiO2/P3HT : PCBM/PEDOT : PSS : AuQD/silver grating structure. The AuQDs were loaded into a hole transport layer (PEDOT : PSS) of the inverted OSCs to increase absorption in the near-ultraviolet (UV) light region and to emit visible light into the neighbouring photoactive layer, thereby achieving light-harvesting improvement of the device. The grating structures were fabricated on P3HT:PCBM layers using a nanoimprinting technique to induce GC-SPR within the inverted OSCs. The AuQDs incorporated within the strongly enhanced GC-SPR evanescent electric field on metallic nanostructures in the inverted OSCs improved the short-circuit current and the efficiency of photovoltaic devices. In comparison with the reference OSC and OSCs with only green AuQDs or only metallic grating, the developed device indicates enhancement of up to 16% power conversion efficiency. This indicates that our light management approach allows for greater light utilization of the OSCs because of the synergistic effect of G-AuQDs and GC-SPR.

Enhancement of organic solar cell performance by incorporating gold quantum dots (AuQDs) on a plasmonic grating.

The incorporation of metallic nanoobjects into devices allows to increase light harvesting, which increases the device performance. In this study, we used a combination of gold quantum dots and grating-coupled surface plasmon resonance (GCSPR) to improve the performance of organic solar cells (OSCs) with a poly(3-hexylthiophene-2,5-diyl) (P3HT):[6,6]-phenyl C61 butyric acid methyl ester (PCBM) photoactive layer. Gold quantum dots with a green fluorescent color (green-AuQD) were loaded into a hole transport layer (HTL) aiming to harvest photons in the UV region and emit visible light into the neighboring photoactive layer. Meanwhile, plasmonic grating structures, which were created on the photoactive layer surfaces via the nanoimprinting technique, provided an enhancement effect through light scattering and GCSPR. Thus, an excellent enhancement of OSC efficiency with a significant increase in short circuit photocurrent (J SC) and power conversion efficiency (PCE) in comparison to that of the reference cell was achieved. The fabricated device provides a J SC value as high as 8.41 mA cm-2 (a 14.11% enhancement) and a PCE value of 3.91% (a 19.57% enhancement). The systematic study clearly reveals that the remarkable enhancement of OSC efficiency is achieved by incorporating both AuQD and plasmonic grating.

Plasmonic-Enhanced Photocurrent Generation of Organic Photovoltaics Induced by 1D Grating and 2D Crossed Grating Structures.

In this work, plasmonic-enhanced photocurrent generation in organic photovoltaic (OPV) devices is demonstrated. One-dimensional (1D) and two-dimensional (2D) crossed grating structures are created on the active-layer surface composed of a blend of poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PC61BM) via a nanoimprinting technique using a template of a Blu-ray disc recordable (BD-R) grating structure. After formation of aluminum back electrodes, the grating-coupled surface plasmon (GCSPR) and light scattering observed in the devices with grating structures provide a 12.3% and 11.0% enhancement of the photocurrent for the devices with 1D grating and 2D crossed grating structures, respectively. The OPV devices with the 2D crossed grating show a plasmonic-enhanced photocurrent under irradiation with light with all polarization directions, whereas those with the 1D grating provide plasmonic enhancement only under illumination with p-polarized light.

Investigation of a gold quantum dot/plasmonic gold nanoparticle system for improvement of organic solar cells.

Light management allows enhancement of light harvesting in organic solar cells (OSCs). In this paper, we describe the investigation of OSCs enhanced by the synergistic effect of gold quantum dots (AuQDs) and localized surface plasmons, obtained by blending a AuQD layer and plasmonic gold nanoparticles (AuNPs) in a hole-transport layer (HTL). Different AuQDs emitting blue, green, and red fluorescence were examined in this study. The OSCs were demonstrated to comprise an ITO-coated glass substrate/AuQDs/PEDOT:PSS:AuNPs/P3HT:PCBM/Al structure. The UV-visible spectra, current density versus voltage characteristics, impedance spectra, and incident photon-to-current efficiency of the fabricated devices were evaluated. The results showed an enhancement of photovoltaic efficiency achieved as a result of the increase in short-circuit current density (J sc) and power conversion efficiency (PCE) in comparison with those of the reference OSCs. The best synergistic effect was found with OSCs consisting of a green-emitting AuQD layer and a HTL containing AuNPs, resulting in the highest improvement in PCE of 13.0%. This indicated that the increase in light harvesting in the developed devices was induced by extended light absorption in the UV region resulting from absorption by the AuQD layer and emission of visible fluorescence from the AuQD layer to the photoactive layers. Moreover, the localized surface plasmon effect of AuNPs, which also contributed to an increase in light trapping in the proposed OSCs, was enhanced by the effect of the AuQDs.

Grating-coupled surface plasmon resonance enhanced organic photovoltaic devices induced by Blu-ray disc recordable and Blu-ray disc grating structures.

In this work, we studied the performance enhancement of organic thin-film solar cells (OSCs) originating from the presence of diffraction gratings on the surface of the active layer. Two types of diffraction gratings, periodic gratings (Blu-ray disc recordable: BD-R) and quasi-random gratings (Blu-ray disc: BD), were employed as master templates for grating structures. The grating structures were introduced to the surfaces of poly(3-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM) films, which were the active layers of the solar cells. The addition of the grating structures led to an increase of light absorption in the absorption region of P3HT:PCBM induced by light scattering. Furthermore, the grating-coupled surface plasmon resonance generated additional light absorption peaks. With illumination of non-polarized light at a normal incident angle, the short-circuit current densities of the BD-R and BD solar cells improved by 11.05% and 10.6%, respectively. Efficiency improvements of 19.28% and 3.21% were also observed for the BD-R and BD devices, respectively. Finally, the finite-difference time-domain simulation results revealed an enhanced electric field in the P3HT:PCBM layer, especially in the BD-R OSC devices.

Inverted organic solar cells enhanced by grating-coupled surface plasmons and waveguide modes.

In this study, we demonstrate improved photovoltaic properties in inverted organic thin-film solar cells by simultaneous excitation of grating-coupled surface plasmons and grating-coupled waveguide modes on gold grating surfaces. The cell consists of a glass-ITO substrate/titanium dioxide/poly(3-hexylthiophene-2,5-diyl):phenyl-C61-butyric acid methyl ester/poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate)/gold structure. The grating structures were fabricated on P3HT:PCBM layers using a nanoimprinting technique with a PDMS stamp. The grating-structured PDMS stamps were fabricated using a DVD-R grating template with a grating pitch, Λ, of 740 nm. Reflectivity measurements made using p-polarized light clearly indicate 2 types of excitation modes, i.e., surface plasmons and waveguide modes, while s-polarized light produces only waveguide modes. Incident photon-to-current efficiency measurements exhibited increased photocurrent wavelengths corresponding to the wavelengths of surface plasmon excitations and waveguide mode excitations. Through the simultaneous excitation of surface plasmons and waveguide modes, short-circuit photocurrents in the grating-structured cells exhibited an improvement of up to 11% in the solar cells, leading to an efficiency increase of 16%.

Effect of urchin-like gold nanoparticles in organic thin-film solar cells.

In this study, urchin-like gold nanoparticles (UL-AuNPs) are used in the fabrication of organic thin-film solar cells (OSCs). UL-AuNPs, which have gold nanothorns on their surface, enhance light accumulation by acting as light-trapping materials. This is due to the enhanced electric field and light scattering attributed to the nanothorns on the surface of the nanoparticles. UL-AuNPs were incorporated into a poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) ( PEDOT: PSS) thin-film layer of organic thin-film solar cells (OSCs). UV-vis spectra, atomic force microscopy (AFM) images, current density versus voltage properties, and the impedance spectra of the fabricated devices were recorded at various concentrations of UL-AuNPs. We found that the efficiency of the OSCs with UL-AuNPs was not only higher than that of a reference cell without nanoparticles but also higher than that of OSCs with spherical AuNPs. Finite-difference time-domain (FDTD) simulation indicated that the electric field around the UL-AuNPs increased due to the presence of nanothorns.

Radical-assisted chemical doping for chemically derived graphene.

Carrier doping of graphene is one of the most challenging issues that needs to be solved to enable its use in various applications. We developed a carrier doping method using radical-assisted conjugated organic molecules in the liquid phase and demonstrated all-wet fabrication process of doped graphene films without any vacuum process. Charge transfer interaction between graphene and dopant molecules was directly investigated by spectroscopic studies. The resistivity of the doped graphene films was drastically decreased by two orders of magnitude. The resistivity was improved by not only carrier doping but the improvement in adhesion of doped graphene flakes. First-principles calculation supported the model of our doping mechanism.

Porous silicon platform for optical detection of functionalized magnetic particles biosensing.

The physical properties of porous materials are being exploited for a wide range of applications including optical biosensors, waveguides, gas sensors, micro capacitors, and solar cells. Here, we review the fast, easy and inexpensive electrochemical anodization based fabrication porous silicon (PSi) for optical biosensing using functionalized magnetic particles. Combining magnetically labeled biomolecules with PSi offers a rapid and one-step immunoassay and real-time detection by magnetic manipulation of superparamagnetic beads (SPBs) functionalized with target molecules onto corresponding probe molecules immobilized inside nano-pores of PSi. We first give an introduction to electrochemical and chemical etching procedures used to fabricate a wide range of PSi structures. Next, we describe the basic properties of PSi and underlying optical scattering mechanisms that govern their unique optical properties. Finally, we give examples of our experiments that demonstrate the potential of combining PSi and magnetic beads for real-time point of care diagnostics.

Doping graphene films via chemically mediated charge transfer.

Transparent conductive films (TCFs) are critical components of a myriad of technologies including flat panel displays, light-emitting diodes, and solar cells. Graphene-based TCFs have attracted a lot of attention because of their high electrical conductivity, transparency, and low cost. Carrier doping of graphene would potentially improve the properties of graphene-based TCFs for practical industrial applications. However, controlling the carrier type and concentration of dopants in graphene films is challenging, especially for the synthesis of p-type films. In this article, a new method for doping graphene using the conjugated organic molecule, tetracyanoquinodimethane (TCNQ), is described. Notably, TCNQ is well known as a powerful electron accepter and is expected to favor electron transfer from graphene into TCNQ molecules, thereby leading to p-type doping of graphene films. Small amounts of TCNQ drastically improved the resistivity without degradation of optical transparency. Our carrier doping method based on charge transfer has a huge potential for graphene-based TCFs.