Resistance to antimalarial drugs is currently a growing public health problem, resulting in more cases with treatment failure. Although previous studies suggested that a concentration gradient facilitates the antibiotic resistance evolution in bacteria, no attempt has been made to investigate the roles of a concentration gradient in malaria drug resistance. Unlike the person-to-person mode of transmission of bacteria, the malaria parasites need to switch back and forth between the human and mosquito hosts to complete the life cycle and to spread the resistant alleles. Here we developed a stochastic combined within- and between-hosts evolutionary dynamics model specific to malaria parasites in order to investigate the influence of an antimalarial concentration gradient on the evolutionary dynamics of malaria drug resistance. Every stage of malaria development in both human and mosquito hosts are individually modelled using the tau-leaping algorithm. We found that the concentration gradient can accelerate antimalarial resistance evolution. The gain in resistance evolution was improved by the increase in the parasite mutation rate and the mosquito biting rate. In addition, even though the rate of resistance evolution is not sensitive to the changes in parasite reduction ratios (PRRs) of antimalarial drugs, the probability of finding the antimalarial drug resistant parasites decreases when the PRR increases.

Solution-processed organic–inorganic hybrid perovskite solar cells are among the candidates to replace the traditional silicon solar cells due to their excellent power conversion efficiency (PCE). Despite this considerable progress, understanding the properties of the perovskite precursor solution is critical for perovskite solar cells (PSCs) to achieve high performance and reproducibility. However, the exploration of perovskite precursor chemistry and its effects on photovoltaic performances has been limited thus far. Herein, we modified the equilibrium of chemical species inside the precursor solution using different photoenergy and heat pathways to identify the corresponding perovskite film formation. The illuminated perovskite precursors exhibited a higher density of high-valent iodoplumbate species, resulting in the fabricated perovskite films with reduced defect density and uniform distribution. Conclusively, the perovskite solar cells prepared by the photoaged precursor solution had not only improved PCE but also enhanced current density, confirmed by device performance, conductive atomic force microscopy (C-AFM), and external quantum efficiency (EQE). This innovative precursor photoexcitation is a simple and effective physical process for boosting perovskite morphology and current density.

Two-photon polymerization (TPP) technologies commonly rely on femtosecond lasers such as Ti:sapphire which limits their accessibility due to high costs and complexities. Recently, multiple reports showed TPP under near-infrared irradiation which enables the use of alternative light sources such as Neodymium-doped lasers known to be affordable and efficient for nanosecond and picosecond pulsed generation. 4,4′-bis(dimethylamino) benzophenone or Michler’s ketone (MK), one of the photoinitiators commonly used for photopolymerization under UV irradiation, also shows an absorption band in the visible region which allows for two-photon polymerization at the fundamental wavelength of Neodymium-doped lasers at 1064 nm. In this report, we investigated the two-photon absorption (TPA) of MK in contrast with Irgacure-784 and Indane-1,3-dione, reported to also be promising photoinitiators for the same TPP process. Among them, MK showed a large TPA cross-section measured via the nonlinear transmission method and Z-scan technique with Q-switched Nd:YAG nanosecond pulse laser at 1064 nm, demonstrating MK as a promising photoinitiator for the low-cost two-photon polymerization.

Two-photon polymerization (TPP) technologies commonly rely on femtosecond lasers such as Ti:sapphire which limits their accessibility due to high costs and complexities. Recently, multiple reports showed TPP under near-infrared irradiation which enables the use of alternative light sources such as Neodymium-doped lasers known to be affordable and e cient for nanosecond and picosecond pulsed generation. 4,4′-bis(dimethylamino) benzophenone or Michler's ketone (MK), one of the photoinitiators commonly used for photopolymerization under UV irradiation, also shows an absorption band in the visible region which allows for two-photon polymerization at the fundamental wavelength of Neodymium-doped lasers at 1064 nm. In this report, we investigated the two-photon absorption (TPA) of MK in contrast with Irgacure-784 and Indane-1,3-dione, reported to also be promising photoinitiators for the same TPP process. Among them, MK showed a large TPA cross-section measured via the nonlinear transmission method and Z-scan technique with Q-switched Nd:YAG nanosecond pulse laser at 1064 nm, demonstrating MK as a promising photoinitiator for the low-cost two-photon polymerization.