High-efficiency and stable piezo-phototronic organic perovskite solar cell

Perovskite materials are regarded as next-generation organic photovoltaic (OPV) materials due to their excellent physical and chemical properties. Recent theoretical and experimental advances also revealed the piezoelectric properties of CH₃NH₃PbI₃ perovskite thin films. In this work, a CH₃NH₃PbI₃ perovskite piezo-phototronic solar cell is studied in theory. The output parameters such as open circuit voltage, current–voltage characteristics, fill factor, power conversion efficiency, and maximum output power with external strains are presented. The coefficient to characterize piezo-phototronic modulation is also calculated for the piezo-phototronic solar cell. With the change of strain, the output performance can be controlled and enhanced. This principle can offer not only a novel and unique approach to produce high-performance, stable perovskite solar cells, but also a principle to design new piezoelectric perovskite optoelectronic devices.

Enhancing the performance of perovskite solar cells with strain based on a piezo-phototronic effect.     

New insights into the treatment of real N,N-dimethylacetamide contaminated wastewater using a membrane bioreactor and its membrane fouling implications

Treatment of N,N-dimethylacetamide (DMAC) wastewater is an important step in achieving the sustainable industrial application of DMAC as an organic solvent. This is the first time that treatment of a high concentration of DMAC in real wastewater has been assessed using membrane bioreactor technology. In this study, an anoxic–oxic membrane bioreactor (MBR) was operated over a month to mineralize concentrated DMAC wastewater. Severe membrane fouling occurred during the short-term operation of the MBR as the membrane flux decreased from 11.52 to 5.28 L (m² h)⁻¹. The membrane fouling was aggravated by the increased amount of protein fractions present in the MBR mixed liquor. Moreover, results from the excitation–emission matrix analysis identified tryptophan and other protein-like related substances as the major membrane-fouling components. Furthermore, analysis of the DMAC degradation mechanism via high performance liquid chromatography (HPLC) and ion chromatography (IC) revealed that the major degradation products were ammonium and dimethylamine (DMA). Although the MBR system achieved the steady removal of DMAC and chemical oxygen demand (COD) by up to 98% and 80%, respectively at DMAC₀ ≤ 7548 mg L⁻¹, DMA was found to have accumulated in the treated effluent. Our investigation provides insight into the prospect and challenges of using MBR systems for DMAC wastewater degradation.

Treatment of N,N-dimethylacetamide (DMAC) wastewater is an important step in achieving the sustainable industrial application of DMAC as an organic solvent.     

3D Pd/Co core–shell nanoneedle arrays as a high-performance cathode catalyst layer for AAEMFCs

A novel cathode architecture using vertically aligned Co nanoneedle arrays as an ordered support for application in alkaline anion-exchange membrane fuel cells (AAEMFCs) has been developed. The Co nanoneedle arrays were directly grown on a stainless steel sheet via a hydrothermal reaction and then a Pd layer was deposited on the surface of the Co nanoneedle arrays using a vacuum sputter-deposition method to form Pd/Co nanoneedle arrays. After transferring the Pd/Co nanoneedle arrays to an AAEM, a cathode catalyst layer was formed. Without the use of an alkaline ionomer, the AAEMFC with the prepared cathode catalyst layer showed an enhanced performance with ultra-low Pd loading of down to 33.5 μg cm⁻², which is much higher than the conventionally used cathode electrode with a Pt loading of 100 μg cm⁻². This is the first report where three-dimensional Co nanoneedle arrays have been used as the cathode support in an AAEMFC, which is able to deliver a higher power density without an alkaline ionomer than that of conventional membrane electrode assembly (MEA).

A novel ordered Pd/Co nanoneedle array was used as a cathode in an AAEMFC and delivered a higher power density than that of conventional MEA.     

Polymeric micro/nanoparticles: Particle design and potential vaccine delivery applications

Particle based adjuvant showed promising signs on delivering antigen to immune cells and acting as stimulators to elicit preventive or therapeutic response. Nevertheless, the wide size distribution of available polymeric particles has so far obscured the immunostimulative effects of particle adjuvant, and compromised the progress in pharmacological researches. To conquer this hurdle, our research group has carried out a series of researches regarding the particulate vaccine, by taking advantage of the successful fabrication of polymeric particles with uniform size. In this review, we highlight the insight and practical progress focused on the effects of physiochemical property (e.g. particle size, charge, hydrophobicity, surface chemical group, and particle shape) and antigen loading mode on the resultant biological/immunological outcome. The underlying mechanisms of how the particles-based vaccine functioned in the immune system are also discussed. Based on the knowledge, particles with high antigen payload and optimized attributes could be designed for expected adjuvant purpose, leading to the development of high efficient vaccine candidates.     

sIPV process development for costs reduction

Polio is expected to be eradicated within only a few years from now. Upon polio eradication, the use of oral polio vaccines, which can cause circulating and virulent vaccine derived polio viruses, will be stopped. From this moment onwards, inactivated polio vaccines (IPV) will be used for worldwide vaccination against polio. An increased demand for IPV is thus anticipated. As a result, process development studies regarding the IPV production process, developed in the 1960s, have intensified. Studies on yield optimization aiming at costs reduction as well as the use of alternative polio viruses, which are more biosafe for manufacturing, are actual. Here our strategy to setup a new IPV production process using attenuated Sabin polio virus strains is presented. Moreover, aspects on reduction of the costs of goods and the impact of process optimization on sIPV costs are reviewed.     

Performance and mechanism of free nitrous acid on the solubilization of waste activated sludge

Free nitrous acid (FNA) is a promising chemical reagent for excess sludge reduction. The distinctive properties of FNA treatment on waste activated sludge (WAS) disposal have previously been demonstrated, however, the cellular response, permeabilization, and disruption caused by low-concentration FNA and the direct cell solubilization of WAS using concentrated FNA should be better understood. In this study, the parameters that influence the sludge solubilization efficiency were optimized over a wide range of FNA concentrations. The sludge solubilization efficiency was found to be superior when the sludge was exposed to FNA (when the dosage of NaNO₂ was 0.12 g g⁻¹ TSS and the pH was 3.0, FNA = 20.94 mg L⁻¹) for 10 h at 25 °C, and the TSS removal and COD dissolution efficiencies were found to be prominent at 38% and 7%, respectively. In the FNA treatment of WAS, some FNA-tolerable cells increased the K⁺, Ca²⁺, and H⁺ effluxes under low concentrations of FNA, and finally achieved ion homeostasis based on the results using a scanning ion-selective electrode measurement technique. This could cause the cells in WAS to maintain cytoactivity and integrity under a low-concentration FNA treatment. Furthermore, flow cytometry was used to assess the permeabilization and disruption of sludge cells toward a concentration gradient of FNA. Flow cytometry results indicated that cells in sludge flocs were disrupted within 30 minutes when the FNA concentration was above 8 mg L⁻¹.

The mechanism of sludge solubilization induced by free nitrous acid over a large concentration range was investigated using SIET and FCM.     

Bio-guided isolation of plant growth regulators from allelopathic plant-Codonopsis pilosula: phyto-selective activities and mechanisms

Natural pesticides are the subject of growing interest, as the overuse of synthetic pesticides severely threatens the safety of humans and the eco-environment. Allelopathic plants can release plentiful secondary metabolites as natural plant growth regulators to affect the growth of neighboring plants. Bio-guided isolation of the aerial waste part of typical allelopathic plant-Codonopsis pilosula led to six active compounds being produced, including ginsenoside Rg₁ (1), ginsenoside Re (2), luteolin (3), luteolin-5-O-glucoside (4), ginsenoside Rb₁ (5) and lobetyolin (6). Ginsenosides and luteolin-5-O-glucoside were firstly found in Codonopsis. Phyto-activity tests showed that all compounds showed inhibiting effects toward C. pilosula, and compounds 2, 4, 5 and 6 were also inhibitors of Amaranthus retroflexus. By contrast, the compounds promoted the seedling growth of wheat, rice and Setaria viridis. At certain concentrations, compounds 1, 4, 5 and 1, 2, 4 could observably promote the growth of wheat and rice seedlings, respectively, exceeding Setaria viridis. The different effects toward the two weeds might be related to the different ROS levels induced by the compounds. The ROS amounts in the root tips of S. viridis were as low as those in the control test, and the ROS content in the root tips increased with aggravation of the inhibition effect. In summary, successful isolation of phyto-selective chemicals from allelopathic plants may provide a promising method for natural herbicide screening. The compounds isolated could potentially be applied as inhibitors of dicotyledon weeds and promoters of monocotyledon crops for weed management in agriculture.

Bio-guided isolation of the aerial waste part of typical allelopathic plant-Codonopsis pilosula led to six active compounds being produced.     

Polarization-independent enhancement of graphene plasmons by coupling with the dipole-like near field of the metallic split-mesh structure

The localized electric field enhancement of graphene plasmon modes is limited by the duty cycle of graphene, the frequency, the absorption and the scattering rate. To obtain higher detectivity, higher field enhancement is required. While the absorption can be no larger than 100%, the scattering is an intrinsic limitation, and the frequency is designated, the duty cycle is the only parameter that can be designed freely to achieve high field enhancement. By etching graphene into periodic structures, i.e. reducing the duty cycle of graphene, the localized electric field can be enhanced as a result of the reduction of the active region. However, too small a duty cycle will weaken the coupling efficiency, which will reduce the absorption, and then the localized electric field can hardly be further enhanced. In this work, we propose to use the metallic split-mesh structure which will focus the incident radiation at the ends of the metallic bars. The absorption and the electric field will be greatly enhanced by placing graphene structures below the small holes formed by the metallic split-mesh structure.

Enhancing the localized electric field of graphene plasmons with a metallic split-mesh structure by more than an order of magnitude.     

The formation and growth of calcium sulfate crystals through oxidation of SO2 by O3 on size-resolved calcium carbonate

Calcium sulfate is a major constituent of atmospheric sulfate, with a typical rod-like morphology ranging from several hundred nanometers to approximately two micrometers observed in field studies. However, the chemical formation mechanism is still not well known. In this study, the kinetics and mechanism for the formation and growth of rod-like calcium sulfate crystals through oxidation of SO₂ by O₃ on size-resolved CaCO₃ at different relative humidity (RH) were investigated using diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and scanning electron microscopy (SEM). We found that the concentration and formation rate of sulfate decreased with the increasing diameter of CaCO₃ particles, and thus smaller particles could enhance the formation of sulfate due to more reactive sites on smaller particles. The rod-like calcium sulfate crystals were formed only at RH above 60% and in the presence of reactant gases through the heterogeneous pathway. The liquid-like water layer formed by promotion of high RH in the presence of reactant gases could facilitate the formation and aggregation of calcium sulfate hydrates and thus promote the formation and growth of rod-like calcium sulfate crystals. This study provides a possible mechanism for the formation and growth of rod-like calcium sulfate crystals existing in the atmosphere.

The heterogeneous formation pathway of rod-like calcium sulfate crystals in the atmosphere.