Leveraging in-situ formation of Ni–Fe nanoparticles to promote the catalytic performance of Ruddlesden-Popper based electrode for symmetrical solid oxide fuel cells

Ruddlesden?Popper layered oxide, La_0.25Sr_2.75FeNiO_7-δ (LSFN) is evaluated as a potential electrode material for symmetrical solid oxide fuel cells. The in-situ formation of Ni–Fe alloy nanoparticles on the LSFN surface in reducing atmosphere can be believed to enhance the activity towards hydrogen oxidation reaction. LSFN exhibit maximum conductivity of 221.2 S/cm and 0.206 S/cm in air and hydrogen environment. Furthermore, LSFN is mixed with GDC powder to form a composite electrode for symmetric solid oxide fuel cells (SSOFC). Results show that with the combination of GDC, the maximum power density of YSZ-based SSOFC enlarges from 232.3 mW cm^?2 to 348.5 mW cm^?2, and related polarization resistance reduces from 0.359 Ω cm² to 0.108 Ω cm². The improved performance is attributed to the enlarged triple-phase boundary with the mixing of GDC. In addition, YSZ-based SSOFC with the LSFN-GDC composite electrode shows a stable performance in intermediate-temperature SSOFCs within 200 h, which indicates that LSFN-GDC composite material is a prospective symmetrical electrode for SSOFC.     

Technological Implications of Modifying the Extent of Cell Wall-Proanthocyanidin Interactions Using Enzymes

The transference and reactivity of proanthocyanidins is an important issue that affects the technological processing of some fruits, such as grapes and apples. These processes are affected by proanthocyanidins bound to cell wall polysaccharides, which are present in high concentrations during the processing of the fruits. Therefore, the effective extraction of proanthocyanidins from fruits to their juices or derived products will depend on the ability to manage these associations, and, in this respect, enzymes that degrade these polysaccharides could play an important role. The main objective of this work was to test the role of pure hydrolytic enzymes (polygalacturonase and cellulose) and a commercial enzyme containing these two activities on the extent of proanthocyanidin-cell wall interactions. The results showed that the modification promoted by enzymes reduced the amount of proanthocyanidins adsorbed to cell walls since they contributed to the degradation and release of the cell wall polysaccharides, which diffused into the model solution. Some of these released polysaccharides also presented some reactivity towards the proanthocyanidins present in a model solution.     

Recent progress in high efficiency polymer solar cells by rational design and energy level tuning of low bandgap copolymers with various electron-withdrawing units

AbstractThis review collects recent five-year publications on low bandgap semiconducting polymers, which are composed of electron donor (D) and electron acceptor (A) units, exhibiting the power conversion efficiency (PCE) higher than 6%. When the photovoltaic performances of different types of D−A semiconducting copolymers are compared after the copolymers are classified into several categories according to the type of A-units, it is realized that diketopyrrolopyrrole (DPP)-based copolymers exhibit high J_SCs owing to low bandgaps and low V_OCs due to high-lying HOMO levels, while thienopyrroledione (TPD)-based copolymers exhibit high V_OCs due to their deep HOMO levels and low J_SCs because of wide bandgaps. Benzothiadiazole- and thienothiophene-based copolymers show intermediate values of V_OC and J_SC between DPP- and TPD-based ones. For further enhancement of photovoltaic performance, DPP-based copolymers may be designed to have deeper HOMO level with the minimum widening of bandgap while TPD-based polymers may be designed to have lower bandgap with the minimum rise of HOMO level. Hence, the energy level tuning must be considered so as to minimize the adverse effect.     

Pd coated one-dimensional Ag nanostructures: Controllable architecture and their electrocatalytic performance for ethanol oxidation in alkaline media

One-dimensional (1D) metal-coated Pd structures are efficient catalysts for the ethanol electro-oxidation and promising strategy for minimizing the Pd-loading toward commercialization of direct ethanol fuel cells (DEFCs). Herein, the decorated and core-shell architectures of a novel Pd coating on Ag nanowires (PdAg-NWs) are controllable by a two-step polyol method based on the galvanic replacement reaction. The integration of uniform shell with a low Pd concentration and partial hollow structure onto 1D PdAg-NWs exhibits the highest efficiency for ethanol oxidation reaction (EOR) in alkaline solution. In comparison with Pd nanoparticles (PdNPs/C), the PdAgNWs/C performes 11 times superior EOR activity, and the onset potential shifts 80 mV negatively. The presence of Ag in PdAg-NWs enhances the absorption capacity of ethanol molecules and hydroxyl ions on the active sites, and improves the catalyst tolerance to CO-like intermediates, making them a potential anodic catalyst for DEFCs.     

In situ vapor-deposited parylene substrates for ultra-thin,lightweight organic solar cells

We fabricate the thinnest (1.3 μm) and lightest (3.6 g/m²) solar cells yet demonstrated, with weight-specific power exceeding 6 W/g, in order to illustrate the lower limits of substrate thickness and materials use achievable with a new processing paradigm. Our fabrication process uniquely starts with growth of an ultra-thin flexible polymer substrate in vacuum, followed by deposition of electrodes and photoactive layers in situ. With this process sequence, the entire cell—from transparent substrate to active layers to encapsulation—can be fabricated at room temperature without solvents and without breaking vacuum, avoiding exposure to dust and other contaminants, and minimizing damage risk associated with handling of thin substrates. We use in situ vapor-phase growth of smooth, transparent, and flexible parylene-C films to produce ultra-thin, lightweight molecular organic solar cells as thin as 2.3 μm including encapsulation with a second parylene-C film. These parylene-based devices exhibit power conversion efficiencies and fabrication yields comparable to glass-based cells. Flexible solar cells on parylene membranes can be seamlessly adhered to a variety of solid surfaces to provide additive solar power.     

An Equalization Time Reduction Method Using a Pseudo‐Random Number Sequence for a Cell Voltage Equalization Circuit with an LC Series Circuit

When the cells of energy storage devices such as electric double‐layer capacitors are connected in series, it results in voltage imbalance in each cell because of the nonuniform properties of the individual cells. In a previous research, the authors proposed a novel cell voltage equalization circuit using an LC series circuit, and they examined the effectiveness of this circuit. However, the characteristics of the cell voltage equalization operation depend on each cell voltage difference. Therefore, the proposed circuit has a disadvantage that the equalization time tends to be longer than other cell voltage equalization circuits with a boosting circuit. This paper proposes an equalization time reduction method that uses a pseudo‐random number sequence generated by the linear congruential generators. The proposed method can reduce the average equalization time without adding any other active or passive elements. The effectiveness of the proposed method is verified through the experimental results. According to the experimental results, the proposed equalization time reduction method reduces the equalization time to 86.5% of the conventional method.     

Side chain effect on photovoltaic properties of dibenzo[a,c]phenazine based donor–acceptor polymers

The electron–donor polymers containing dibenzo[a,c]phenazine (BPz) derivatives with 2,7-alkyl and 11,12-alkoxy substituted, PBDT-BPzC and PBDT-OBPz, respectively, were synthesized to investigate the photovoltaic effect of different side chain substitutions. The polymers exhibit similar physical properties, except the HOMO and LUMO of PBDT-BPzC are 0.18 and 0.15 eV deeper than PBDT-OBPz, resulting in the V_oc of polymer solar cells (PSCs) based on PBDT-BPzC are above 0.1 V higher than that of PBDT-OBPz. With the contribution of the superior V_oc, polymer PBDT-BPzC showed preferable photovoltaic performances, and the PCE reached 4.44%, which is 0.49% higher than PBDT-OBPz. This research reveals a preferred side chain substituted way to modify BPz unit, and gives an optimally developing the dibenzo[a,c]phenazine derivatives based electron–donor polymers.