Dye-sensitized solar cells (DSCs) offer the possibilities to design solar cells with a large flexibility in shape, color, and transparency. DSC research groups have been established around the worl ...

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Dye-Sensitized Solar Cells

Advanced energy conversion and storage (ECS) devices (including fuel cells, photoelectrochemical water splitting cells, solar cells, Li-ion batteries and supercapacitors) are expected to play a major role in the development of sustainable technologies that alleviate the energy and environmental challenges we are currently facing. The successful utilization of ECS devices depends critically on synthesizing new nanomaterials with merits of low cost, high efficiency, and outstanding properties. Recent progress has demonstrated that nanostructured metal chalcogenides (MCs) are very promising candidates for efficient ECS systems based on their unique physical and chemical properties, such as conductivity, mechanical and thermal stability and cyclability. In this review, we aim to provide a summary on the liquid-phase synthesis, modifications, and energy-related applications of nanostructured metal chalcogenide (MC) materials. The liquid-phase syntheses of various MC nanomaterials are primarily categorized with the preparation method (mainly 15 kinds of methods). To obtain optimized, enhanced or even new properties, the nanostructured MC materials can be modified by other functional nanomaterials such as carbon-based materials, noble metals, metal oxides, or MCs themselves. Thus, this review will then be focused on the recent strategies used to realize the modifications of MC nanomaterials. After that, the ECS applications of the MC/modified-MC nanomaterials have been systematically summarized based on a great number of successful cases. Moreover, remarks on the challenges and perspectives for future MC research are proposed (403 references).

Nanostructured metal chalcogenides: synthesis, modification, and applications in energy conversion and storage devices

Electrocatalysis plays a key role in the energy conversion processes central to several renewable energy technologies that have been developed to lessen our reliance on fossil fuels. However, the best electrocatalysts for these processes—which include the hydrogen evolution reaction (HER), the oxygen reduction reaction (ORR), and the redox reactions that enable regenerative liquid-junction photoelectrochemical solar cells—often contain scarce and expensive noble metals, substantially limiting the potential for these technologies to compete with fossil fuels. The considerable challenge is to develop robust electrocatalysts composed exclusively of low-cost, earth-abundant elements that exhibit activity comparable to that of the noble metals. In this review, we summarize recent progress in the development of such high-performance earth-abundant inorganic electrocatalysts (and nanostructures thereof), classifying these materials based on their elemental constituents. We then detail the most critical obstacles facing earth-abundant inorganic electrocatalysts and discuss various strategies for further improving their performance. Lastly, we offer our perspectives on the current directions of earth-abundant inorganic electrocatalyst development and suggest pathways toward achieving performance competitive with their noble metal-containing counterparts.

Earth-abundant inorganic electrocatalysts and their nanostructures for energy conversion applications

When applied on the counter electrode of a dye-sensitized solar cell, functionalized graphene sheets with oxygen-containing sites perform comparably to platinum (conversion efficiencies of 5.0 and 5.5%, respectively, at 100 mW cm−2 AM1.5G simulated light). To interpret the catalytic activity of functionalized graphene sheets toward the reduction of triiodide, we propose a new electrochemical impedance spectroscopy equivalent circuit that matches the observed spectra features to the appropriate phenomena. Using cyclic voltammetry, we also show that tuning our material by increasing the amount of oxygen-containing functional groups can improve its apparent catalytic activity. Furthermore, we demonstrate that a functionalized graphene sheet based ink can serve as a catalytic, flexible, electrically conductive counter electrode material.

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Functionalized graphene as a catalytic counter electrode in dye-sensitized solar cells.

A composite film of nickel sulfide/platinum/titanium foil (NiS/Pt/Ti) with low cost and high electrocatalytic activity was synthesized by the use of an in situ electropolymerization route and proposed as a counter electrode (CE) catalyst for flexible dye-sensitized solar cells (FDSSCs). The FDSSC with the NiS/Pt/Ti CE exhibited a comparable power conversion efficiency of 7.20% to the FDSSC with the platinum/titanium (Pt/Ti) CE showing 6.07%. The surface morphology of the NiS/Pt/Ti CE with one-dimensional (1D) structure is characterized by using the scanning electron microscopy (SEM). The NiS/Pt/Ti CE also displayed multiple electrochemical functions of excellent conductivity, great electrocatalytic ability for iodine/triiodine, and low charge transfer resistance of 2.61 ± 0.02 Ω cm2, which were characterized by using the cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and Tafel polarization plots. The photocurrent-photovoltage (J-V) character curves were further used to calculate the theoretical optical light performance parameters of the FDSSCs. It may be said that the NiS/Pt/Ti counter electrode is a promising catalytic material to replace the expensive platinum in FDSSCs.

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A highly efficient flexible dye-sensitized solar cell based on nickel sulfide/platinum/titanium counter electrode

Nickel sulfides have been, for the first time, electrodeposited on transparent conductive glass by a facile periodic potential reversal (PR) technique to supersede Pt counter electrodes (CEs) of dye-sensitized solar cells (DSCs). The composition and electrochemical catalytic activity of the nickel sulfide films prepared by PR technique are different from those of the ones deposited by the commonly used potentiostatic (PS) technique. PR technique produces transparent single-component NiS, while co-deposition of Ni and NiS is found in the opaque films prepared by PS method. The nickel sulfide deposited by PR technique shows high catalytic activity for the reduction of I3− to I− in a DSC. DSC with the CE deposited by PR technique performs much better (6.82%) than that by PS method (3.22%), and is comparable to the device with conventional Pt coated CE (7.00%).

Dye-sensitized solar cells with NiS counter electrodes electrodeposited by a potential reversal technique

A flexible carbon counter electrode for dye-sensitized solar cells

At present, the photovoltaic performance of quantum dot-sensitized solar cells (QDSCs) is still much lower than conventional DSCs. Appropriate porous TiO2 photoanodes for QDSCs need to be further investigated, and optimization of the nanoparticle-based photoanodes is highly desirable as well. In this article, the influence of the structural properties of various TiO2 photoanodes on CdS/CdSe-sensitized solar cells have been systematically studied. Quantitative analyses of light-harvesting efficiency (LHE) and electron-transfer yield (ΦET) for the QDSCs are investigated for the first time. It is revealed that the LHE increases in the long wavelength region with the addition of large size TiO2 particles to the transparent film. In the meantime, the balance between the light scattering and surface area also needs to be controlled, which can significantly restrain the dark current of the device. A double-layer photoanodic structure can give 4.92% of light-to-electricity conversion efficiency with a photoactive area of 0.15 cm2.

Highly efficient CdS/CdSe-sensitized solar cells controlled by the structural properties of compact porous TiO2 photoelectrodes

Application of carbon counterelectrode on CdS quantum dot-sensitized solar cells (QDSSCs)

A new kind of fibrous quantum dot sensitized solar cell has been designed and fabricated by using CdS and CdSe co-sensitized TiO(2) nanotubes on Ti wire as the photoanode and highly active Cu(2)S as the counter electrode. By optimizing the CdSe deposition time and the length of the nanotube, a power conversion efficiency of 3.18% has been obtained under AM 1.5 illumination (100 mW cm(-2)). The potential application of this kind of solar cell has also been discussed in this paper.

http://iopscience.iop.org/article/10.1088/0957-4484/21/37/375201/pdf

Shuqing Huang

Papers

Dye-sensitized solar cells with NiS counter electrodes electrodeposited by a potential reversal technique

A flexible carbon counter electrode for dye-sensitized solar cells

Highly efficient CdS/CdSe-sensitized solar cells controlled by the structural properties of compact porous TiO2 photoelectrodes

Application of carbon counterelectrode on CdS quantum dot-sensitized solar cells (QDSSCs)

Fibrous CdS/CdSe quantum dot co-sensitized solar cells based on ordered TiO2 nanotube arrays