Photoelectric Memory Effect in an Organic Bulk Heterojunction Device

We report on a memory effect observed in an inverted bulk heterojunction organic photovoltaic device, where the electron-collecting electrode is ZnO nanowires grown on an indium tin oxide (ITO) substrate. The device presented a unique response to light by switching from a rectifying behavior in the dark to a resistive response under illumination. After cessation of light, the device slowly stabilized back to its rectifying nature after ∼270 min, introducing a volatile photoelectric memory effect. The reversibility of the response is verified through multiple cycles of light exposure and placing the device in the dark. The device is also illuminated with different light intensities to study the photovoltaic response through I–V characterization. It is found that the time constant associated with the transition between the rectifying and resistive characteristics is independent from the light intensity. Further study revealed that there is a hysteresis loop in the I–V curve in the dark, but the loop vanished in the resistive mode under illumination. A mechanism based on oxygen absorption–desorption has been suggested to explain the observed effect. Such a memory effect can be used in various optoelectronic devices to save the optical information for an extended time

Large Photocurrent Response and External Quantum Efficiency in Biophotoelectrochemical Cells Incorporating Reaction Center Plus Light Harvesting Complexes

Bacterial photosynthetic reaction centers (RCs) are promising materials for solar energy harvesting, due to their high ratio of photogenerated electrons to absorbed photons and long recombination time of generated charges. In this work, photoactive electrodes were prepared from a bacterial RC-light-harvesting 1 (LH1) core complex, where the RC is encircled by the LH1 antenna, to increase light capture. A simple immobilization method was used to prepare RC-LH1 photoactive layer. Herein, we demonstrate that the combination of pretreatment of the RC-LH1 protein complexes with quinone and the immobilization method results in biophotoelectrochemical cells with a large peak transient photocurrent density and photocurrent response of 7.1 and 3.5 μA cm^–2, respectively. The current study with monochromatic excitation showed maximum external quantum efficiency (EQE) and photocurrent density of 0.21% and 2 μA cm^–2, respectively, with illumination power of ∼6 mW cm^–2 at ∼875 nm, under ambient conditions. This work provides new directions to higher performance biophotoelectrochemical cells as well as possibly other applications of this broadly functional photoactive material

Hybrid Wiring of the Rhodobacter sphaeroides Reaction Center for Applications in Bio-photoelectrochemical Solar Cells

The growing demand for nonfossil fuel-based energy production has drawn attention to the utilization of natural proteins such as photosynthetic reaction center (RC) protein complexes to harvest solar energy. The current study reports on an immobilization method to bind the wild type Rhodobacter sphaeroides RC from the primary donor side onto a Au electrode using an immobilized cytochrome <i>c</i> (cyt <i>c</i>) protein via a docking mechanism. The new structure has been assembled on a Au electrode by layer-by-layer deposition of a carboxylic acid-terminated alkanethiol (HOOC (CH₂)₅S) self-assembled monolayer (SAM), and layers of cyt <i>c</i> and RC. The Au|SAM|cyt <i>c</i>|RC working electrode was applied in a three-probe electrochemical cell where a peak cathodic photocurrent density of 0.5 μA cm^–2 was achieved. Further electrochemical study of the Au|SAM|cyt <i>c</i>|RC structure demonstrated ∼70% RC surface coverage. To understand the limitations in the electron transfer through the linker structure, a detailed energy study of the SAM and cyt <i>c</i> was performed using photochronoamperometry, ellipsometry, photoemission spectroscopy, and cyclic voltammetry (CV). Using a simple rectangle energy barrier model, it was found that the electrode work function and the large barrier of the SAM are accountable for the low conductance in the devised linker structure

Sequential Laser-Burned Lignin and Hydrogen Evolution-Assisted Copper Electrodeposition to Manufacture Wearable Electronics

In the contemporary world, wearable electronics and smart textiles/fabrics are galvanizing a transformation of the health care, aerospace, military, and commercial industries. However, a major challenge that exists is the manufacture of electronic circuits directly on fabrics. In this work, we addressed the issue by developing a sequential manufacturing process. First, the target fabric was coated with a customized ink containing lignin. Next, a desired circuit layout was patterned by laser burning lignin, converting it to carbon and establishing a conductive template on the fabric. At last, using an in-house-designed printer, a devised localized hydrogen evolution-assisted (HEA) copper electroplating method was applied to metalize the surface of the laser-burned lignin pattern to achieve a very low resistive circuit layout (0.103 Ω for a 1 cm long interconnect). The nanostructure and material composition of the different layers were investigated via scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and Fourier-transform infrared spectroscopy (FTIR). Monitoring the conductivity change before and after bending, rolling, stretching, washing, and adhesion tests presented remarkable mechanical stability due to the entanglement of the copper nanostructure to the fibers of the fabric. Furthermore, the HEA method was used to solder a light-emitting diode to a patterned circuit on the fabric by growing copper at the terminals, creating interconnects. The presented sequential printing method has the potential for fabricating reliable wearable electronics for various applications, particularly in medical monitoring

Sequential Laser-Burned Lignin and Hydrogen Evolution-Assisted Copper Electrodeposition to Manufacture Wearable Electronics

In the contemporary world, wearable electronics and smart textiles/fabrics are galvanizing a transformation of the health care, aerospace, military, and commercial industries. However, a major challenge that exists is the manufacture of electronic circuits directly on fabrics. In this work, we addressed the issue by developing a sequential manufacturing process. First, the target fabric was coated with a customized ink containing lignin. Next, a desired circuit layout was patterned by laser burning lignin, converting it to carbon and establishing a conductive template on the fabric. At last, using an in-house-designed printer, a devised localized hydrogen evolution-assisted (HEA) copper electroplating method was applied to metalize the surface of the laser-burned lignin pattern to achieve a very low resistive circuit layout (0.103 Ω for a 1 cm long interconnect). The nanostructure and material composition of the different layers were investigated via scanning electron microscopy, energy-dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and Fourier-transform infrared spectroscopy (FTIR). Monitoring the conductivity change before and after bending, rolling, stretching, washing, and adhesion tests presented remarkable mechanical stability due to the entanglement of the copper nanostructure to the fibers of the fabric. Furthermore, the HEA method was used to solder a light-emitting diode to a patterned circuit on the fabric by growing copper at the terminals, creating interconnects. The presented sequential printing method has the potential for fabricating reliable wearable electronics for various applications, particularly in medical monitoring

The Role of Gold-Adsorbed Photosynthetic Reaction Centers and Redox Mediators in the Charge Transfer and Photocurrent Generation in a Bio-Photoelectrochemical Cell

Bacterial photosynthetic reaction centers (RCs) are promising materials for solar energy harvesting, due to their high quantum efficiency. A simple approach for making a photovoltaic device is to apply solubilized RCs and charge carrier mediators to the electrolyte of an electrochemical cell. However, the adsorption of analytes on the electrodes can affect the charge transfer from RCs to the electrodes. In this work, photovoltaic devices were fabricated incorporating RCs from purple bacteria, ubiquinone-10 (Q2), and cytochrome c (Cyt c) (the latter two species acting as redox mediators). The adsorption of each of these three species on the gold working electrode was investigated, and the roles of adsorbed species in the photocurrent generation and the cycle of charge transfer were studied by a series of photochronoamperometric, X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and cyclic voltammetry (CV) tests. It was shown that both redox mediators were required for photocurrent generation; hence, the RC itself is likely unable to inject electrons into the gold electrode directly. The reverse redox reactions of mediators at the electrodes generates electrical current. Cyclic voltammograms for the RC-exposed gold electrode revealed a redox couple due to the adsorbed RC at ∼ +0.5 V (vs NHE), which confirmed that the RC was still redox active, upon adsorption to the gold. Photochronoamperometric studies also indicated that RCs adsorb, and are strongly bound to the surface of the gold, retaining functionality and contributing significantly to the process of photocurrent generation. Similar experiments showed the adsorption of Q2 and Cyt c on unmodified gold surfaces. It was indicated by the photochronoamperometric tests that the photocurrent derives from Q2-mediated charge transfer between the RCs and the gold electrode, while solubilized Cyt c mediates charge transfer between the P-side of adsorbed RC and the Pt counter electrode. Also, the stability of the adsorbed RCs and mediators was evaluated by measuring the photocurrent response over a period of 1 week. It is found that ∼46% of the adsorbed RCs remain active after a week under aerobic conditions. A significantly extended lifetime is expected by removing oxygen from the electrolyte and sealing the device