Uniform-size rutile TiO2 microrods were synthesized by simple molten-salt method with sodium chloride as reacting medium and different kinds of sodium phosphate salts as growth control additives to control the one-dimensional (1-D) crystal growth of particles. The effect of rutile and anatase ratios as a precursor was monitored for rod growth formation. Apart from uniform rod growth study, optical properties of rutile microrods were observed by UV−visible and photoluminescence (PL) spectroscopy. TiO2 materials with anatase and rutile phase show PL emission due to self-trapped exciton. It has been observed that synthesized rutile TiO2 rods show various PL emission peaks in the range of 400 to 900 nm for 355 nm excitation wavelengths. All PL emission appeared due to the oxygen vacancy present inside rutile TiO2 rods. The observed PL near the IR range (785 and 825 nm) was due to the formation of a self-trapped hole near to the surface of (110) which is the preferred orientation plane of synthesized rutile TiO2 microrods.

Organocatalyzed atom transfer radical polymerization (O-ATRP) with light, acting as photoredox catalysis, is growing to be one of the emerging fields of photocatalysis and chemical transformations due to the mild, environment-friendly, and light-control manners. To screen much more effective metal-free photocatalysts and the exact functions of different fragments in organic molecular photocatalysts, this report selected Nunsubstituted diketopyrrolopyrrole (DPP) analogues and figured out the structure− properties relationship and the catalytic mechanism. The results revealed the key role of the N-unsubstituted DPP core in the charge transfer, singlet/triplet formation, and intermediate formation. Furthermore, the DPP core acted as the function of reductive reaction initiators with reductive potentials, while the adjacent groups tuned oxidative potentials and stability of the radical cations and simultaneously controlled the oxidative quenching deactivation process through the bromide (−Br) intermediates of doublet complexes. The systematic inspection of the atomic active sites of photoredox catalysts has so far not been taken into consideration regarding both the experimental and theoretical examination. The findings about these novel DPP photoredox catalysts will aid in the rational search for much more effective organophotoredox metal-free compounds for use in controlled radical polymerization and other organic transformations.

SmCo5 and SmCo5−xCux magnetic particles were produced by co-precipitation followed by reduction diffusion. HRTEM confirmed the Cu substitution in the SmCo5 lattice. Non-magnetic Cu was substituted at “2c” site in the SmCo5 crystal lattice and effectively stopped the coupling in its surroundings. This decoupling effect decreased magnetic moment from SmCo5 (12.86 μB) to SmCo4Cu (10.58 μB) and SmCo3Cu2 (7.79 μB) and enhanced anisotropy energy from SmCo5 (10.87 Mega erg/cm3) to SmCo4Cu (14.05 Mega erg/cm3) and SmCo3Cu2 (14.78 Mega erg/cm3). Enhancement of the anisotropy energy increased the coercivity as its values for SmCo5, SmCo4Cu and SmCo3Cu2 were recorded as 4.5, 5.97 and 6.99 kOe respectively. Being six times cheaper as compared to Co, substituted Cu reduced the price of SmCo3Cu2 up to 2%. Extra 15% Co was added which not only enhanced the Mr value but also reduced the 5% of the total cost because of additional weight added to the SmCo3Cu2. Method reported in this work is most energy efficient method on the synthesis of Sm–Co–Cu ternary alloys until now.

Nd2Fe14B is one of the most popular permanent magnets (PMs) possessing the best energy product (BH)max among the common PM materials.

Nitrogen-enriched polytriazine (NPT), a carbon nitride-based material, has received much attention for CO2 storage applications. However, to enhance the CO2 uptake capacity more efficiently, it is necessary to understand the interaction mechanism between CO2 molecules and NPT through appropriate modification of the structures. Here, we introduce a method to enhance the CO2 adsorption capacity of NPT by incorporating metal atoms such as Sn, Co, and Ni into the polytriazine network. DFT calculations were used to investigate the CO2 adsorption mechanism of the polytriazine frameworks by tracking the interactions between CO2 and the various interaction sites of NPT. By optimizing the geometry of the pure and metal-containing NPT frameworks, we calculated the binding energy of metal atoms in the NPT framework, the adsorption energy of CO2 molecules, and the charge transfer between CO2 molecules and the corresponding adsorption systems. In this work, we demonstrate that the CO2 adsorption capacity of NPT can be greatly enhanced by doping transition-metal atoms into the cavities of NPT.