Dual-Strategy Tailoring Molecular Structures of Dopant-Free Hole Transport Materials for Efficient and Stable Perovskite Solar Cells.

Dopant-free hole transport materials (HTMs) are ideal materials for highly efficient and stable n-i-p perovskite solar cells (PSCs), but most current design strategies for tailoring the molecular structures of HTMs are limited to single strategy. Herein, four HTMs based on dithienothiophenepyrrole (DTTP) core are devised through dual-strategy methods combining conjugate engineering and side chain engineering. DTTP-ThSO with ester alkyl chain that can form six-membered ring by the S⋅⋅⋅O noncovalent conformation lock with thiophene in the backbone shows good planarity, high-quality film, matching energy level and high hole mobility, as well as strong defect passivation ability. Consequently, a remarkable power conversion efficiency (PCE) of 23.3 % with a nice long-term stability is achieved by dopant-free DTTP-ThSO-based PSCs, representing one of the highest values for un-doped organic HTMs based PSCs. Especially, the fill factor (FF) of 82.3 % is the highest value for dopant-free small molecular HTMs-based n-i-p PSCs to date. Moreover, DTTP-ThSO-based devices have achieved an excellent PCE of 20.9 % in large-area (1.01 cm2) devices. This work clearly elucidates the structure-performance relationships of HTMs and offers a practical dual-strategy approach to designing dopant-free HTMs for high-performance PSCs.

Novel Pyrimidine-Based Iridium Complexes with Bulky Charge-Carrier Groups as Dopants for Highly Efficient Green Polymer Light-Emitting Diodes.

Two new pyrimidine-based iridium complexes with triphenylamine and tetraphenylsilane, namely (TPAPr)2 IrAcac and (TPSPr)2 IrAcac, were fully synthesized and characterized. Both of the targeted iridium complexes exhibit excellent thermal stability and high photoluminescence quantum yields. Compared to (TPAPr)2 IrAcac, (TPSPr)2 IrAcac achieved its highest PLQY and current efficiency (CE) at higher dopant concentration probably because of its bulky tetraphenylsilane group, which can effectively suppress the concentration quenching. However, according to DFT studies, (TPSPr)2 IrAcac shows faster non-radiative transitions due to the presence of more excited-state distortions than (TPAPr)2 IrAcac. As a result, Green phosphorescent polymer light-emitting diodes (PLEDs) containing (TPAPr)2 IrAcac and (TPSPr)2 IrAcac as dopants exhibit exceptional device performance with peak CE values of 38.24 and 36.06 cd A-1 , respectively. (TPAPr)2 IrAcac exhibited a superior efficiency than (TPSPr)2 IrAcac because of its high Φp , low RMSD value, and efficient energy transfer from the host to the guest. More importantly, the PLEDs based on (TPAPr)2 IrAcac and (TPSPr)2 IrAcac show stable phosphorescent emission with Commission Internationale de L'Eclairage (CIE) coordinates of (0.313, 0.497) and (0.299, 0.483), respectively. This work points out a viable method for creating phosphorescent iridium complexes based on pyrimidine for high-efficiency organic light-emitting diodes (OLEDs).

High Cycling Stability of the LiNi0.8 Co0.1 Mn0.1 O2 Cathode via Surface Modification with Polyimide/Multi-Walled Carbon Nanotubes Composite Coating.

The Ni-rich LiNi0.8 Co0.10 Mn0.1 O2 (NCM811) cathode coated by combining with multi-walled carbon nanotubes (MWCNTs) and polyimide (PI) produces a PI3-NCM811 cathode, which markedly improves cycling stability and suppresses secondary crystal cracking. The initial discharge capacity of the PI3-NCM811 cathode is 199.6 mAh g-1 between 2.8 and 4.3 V at 0.1 C @ 25 °C, which is slightly lower than that of NCM811 (201.1 mAh g-1 ). The PI3-NCM811 and NCM811 cathodes keep 90.6% and 64.8% of their initial discharge capacity at 1 C between 2.8 and 4.3 V after 500 cycles, respectively. Furthermore, the difference (21.1%) in capacity retention rate between PI3-NCM811 and NCM811 under the condition of 2.8-4.5 V became smaller compared with the difference (25.8%) under the condition of 2.8-4.3 V. This better cyclic stability is mainly attributed to the toughness and elasticity of PI, which inhibits the secondary cracking, maintains the structural integrity of the cathode particles, and protects the particles from electrolyte damage during long-term cycling.

A Water-Stable Anionic Metal-Organic Framework Constructed from Columnar Zinc-Adeninate Units for Highly Selective Light Hydrocarbon Separation and Efficient Separation of Organic Dyes.

A metal-organic framework (MOF), {(Me2NH2)2[Zn6(µ4-O)(ad)4(BPDC)4]}n (JXNU-4; ad- = adeninate), with an anionic three-dimensional (3D) framework constructed from one-dimensional (1D) columnar [Zn6(ad)4(µ4-O)]n secondary building units (SBUs) and 4,4'-biphenyldicarboxylate (BPDC2-) ligand, was prepared. The anionic 3D framework has 1D square channels with an aperture of about 9.8 Å and exhibits a carboxylate-O-decorated pore environment. The microporous nature of JXNU-4 was established by the N2 adsorption data, which gives Langmuir and Brumauer-Emmett-Teller surface areas of 1800 and 1250 m2 g-1, respectively. Noticeably, JXNU-4 shows potential as a separation agent for the selective removal of propane and ethane from natural gas with high selectivities of 144 for C3H8/CH4 (5:95) and 14.6 for C2H6/CH4 (5:95), respectively. Most importantly, JXNU-4 shows an aqueous-phase adsorption of a positively charged ion of methylene blue selectively over a negatively charged ion of resorufin, which is pertinent to the anionic nature of the framework, and provides a size-exclusive sieving of methylene blue over other positively charged ions of Janus Green B and ethyl violet, which is relevant to its pore structure, enabling the efficient aqueous-phase separation of organic dyes.

Fine-Tuning Ligand to Modulate the Magnetic Anisotropy in a Carboxylate-Bridged Dy2 Single-Molecule Magnet System.

A series of dinuclear Dy(III) compounds with the general formula [Dy2(µ2-anthc)4(anthc)2(L)2] (anthc(-) = 9-anthracenecarboxylate, L = 2,2'-bipyridyl (1), 1,10-phenanthroline (2), and 4,7-dimethyl-1,10-phenanthroline (3)) were synthesized and magnetically characterized. These compounds exhibit single-molecule magnet (SMM) behavior in the absence of the direct-current field, which is rarely observed for carboxylate-bridged dinuclear Dy2 system. With the first coordination sphere of Dy(III) centers being fixed, the energy barrier was modulated by sequentially modifying the terminal neutral L ligands in this Dy2 system. Theoretical calculations revealed that the symmetry of the charge distribution surrounding the Dy(III) centers in 1-3 is the decisive factor to determine the relaxation of the SMMs. The combination of the larger charge distribution along the magnetic axis and lower charge distribution in the equatorial plane (hard plane) formed by five coplanar coordination atoms including two N atoms provided by an L ligand led to a strong easy-axis ligand field in these compounds. This work presents a rational method to modulate the dynamic magnetic relaxation of the lanthanide SMMs through fine-tuning electrostatic potential of the atoms on the hard plane.

Lanthanide-Potassium Biphenyl-3,3'-disulfonyl-4,4'-dicarboxylate Frameworks: Gas Sorption, Proton Conductivity, and Luminescent Sensing of Metal Ions.

A novel sulfonate-carboxylate ligand of biphenyl-3,3'-disulfonyl-4,4'-dicarboxylic acid (H4-BPDSDC) and its lanthanide-organic frameworks {[LnK(BPDSDC)(DMF)(H2O)]·x(solvent)}n (JXNU-2, where JXNU denotes Jiangxi Normal University, DMF indicates dimethylformamide, and Ln = Sm(3+), Eu(3+), and Pr(3+)) were synthesized and structurally characterized. The three isomorphous lanthanide compounds feature three-dimensional frameworks constructed from one-dimensional (1D) rod-shaped heterometallic Ln-K secondary building units and are an illustration of a Kagome-like lattice with large 1D hexagonal channels and small 1D trigonal channels. The porous material of the representive JXNU-2(Sm) has an affinity to quadrupolar molecules such as CO2 and C2H2. In addition, the JXNU-2(Sm) compound exhibits humidity- and temperature-dependent proton conductivity with a large value of 1.11 × 10(-3) S cm(-1) at 80 °C and 98% relative humidity. The hydrophilic sulfonate group on the surface of channels facilitates enrichment of the solvate water molecules in the channels, which enhances the proton conductivity of this material. Moreover, the JXNU-2(Eu) material with the characteristic bright red color shows the potential for recognition of K(+) and Fe(3+) ions. The enhancing Eu(3+) luminescence with the K(+) ion and quenching Eu(3+) luminescence with the Fe(3+) ion can be associated with the functional groups of the organic ligand.

Field-Induced Slow Magnetic Relaxation and Gas Adsorption Properties of a Bifunctional Cobalt(II) Compound.

A new compound, {[Co(bmzbc)2] · 2DMF}n (JXNU-1, JXNU denotes Jiangxi Normal University), based on the 4-(benzimidazole-1-yl)benzoate (bmzbc(-)) ligand has been synthesized and structurally characterized. The Co(II) ions are bridged by the rod-like bmzbc(-) ligands to give a two-dimensional (2D) sheet wherein the Co(II) ions are spatially separated from each other by the long bmzbc(-) rods. The 2D sheets are further stacked into a 3D framework with 1D channels occluding the guest DMF molecules. Detailed magnetic studies show that the individual octahedral Co(II) ions in JXNU-1 exhibit field-induced slow magnetic relaxation, which is characteristic behavior of single-ion magnets (SIMs). The rarely observed positive value of zero-field splitting (ZFS) parameter D for the Co(II) ion in JXNU-1 demonstrates that JXNU-1 is a unique example of Co(II)-based SIMs with easy-plane anisotropy, which is also confirmed by the calculations. The microporous nature of JXNU-1 was established by measuring CO2 sorption isotherms. The abrupt changes observed in the C3H8 and C2H6 adsorption isotherms indicate that a structural transformation occurred in the gas-loading process. The long connection between the magnetic metal centers in JXNU-1 meets the requirements for construction of porosity and SIM in a well-defined network, harmoniously providing a good candidate of functional molecular materials exhibiting SIM and porosity.

Coordination polymer submicrospheres: fast microwave synthesis and their conversion under different atmospheres.

Rare earth (RE) based coordination polymer (CP) submicrospheres have been prepared from pyridine-2,5-dicarboxylic acid and RE(NO3)3 via a facile microwave heating method in 5 min, with N,N-dimethylformamide (DMF) as solvent. The submicrospheres have diameters of 100-400 nm. Furthermore, the surface of the microspheres is smooth and the microspheres are solid. Several CP submicrospheres (RE = La, Gd, Y) were selected and calcined under different atmospheres (including air, N2, and NH3). After calcination in air at 550 °C for 4 h, rare earth oxide (RE2O3) submicrospheres were obtained. On calcination under an N2 atmosphere, LaN/La2O3/C composite spheres were obtained for La-based CPs. For Gd(Y)-based CPs, Gd2O3(Y2O3)/C composite spheres were obtained. Porous carbon submicrospheres were obtained after the removal of RE2O3 and REN from the composite spheres. Interestingly, under an NH3 atmosphere, La2O2CN2 submicrospheres were produced from the La-based CPs. In addition, the Gd-based and Y-based CPs submicrospheres gave Gd2O3/GdN/C and Y2O3/C submicrospheres, respectively. As examples of their potential applications, their upconversion properties and electrochemical properties of the as-prepared products were investigated. This facile microwave synthesis method may offer an attractive approach for the preparation of other RE-CP micro-/nanostructures, and many interesting materials may be derived.

The analysis of the immobilization mechanism of Ni(II) on Bacillus cereus.

This work focused on the identification of biosorption mechanism of Ni(II) by living Bacillus cereus (B. cereus) based on batch experiments and a variety of microscopic equipments. The adsorption equilibrium reached rapidly in 2 h and the maximum nickel adsorption capability of B. cereus was 17.7 mg x g(-1) (dry weight). Atomic force microscopy (AFM) analysis showed that the bacterial surface roughness increased from 7.9 +/- 0.5 nm to 12.6 +/- 1.6 nm during this process. Scanning electron microscopy (SEM) observation confirmed that there was Ni(II) on the bacterial surface. However, transmission electron microscopy (TEM) thin section analysis coupled with energy dispersive X-ray spectroscopy (EDS) revealed that Ni(II) could also be found in the inner portions of the bacteria. Inductive coupled plasma emission spectrometer (ICP-OES) quantitative analysis elucidated that over 70% of the immobilized Ni(II) was binding on the surface of bacteria. X-ray diffraction (XRD) analysis showed that the Ni(II) collected by the bacteria was amorphous. Fourier transform infrared (FT-IR) analysis indicated that amides and carboxylation functional groups might be involved in the coordination of Ni(II).

Evaluation of phase, microstructure and composition of human dentine after Er,Cr:YSGG laser irradiation.

This study aims to evaluate the composition, micro-structure and inorganic phase alternations of human dentine irradiated by Er,Cr:YSGG laser with water cooling spray system. X-ray diffraction (XRD) analysis indicated that the main inorganic phase of dentine before and after laser irradiation were all Hydroxyapatite (HA) structure, approximately 30 nm in size. No significant changes occurred in the average particle size after irradiation in four energy densities (6.18 J/cm2, 8.04 J/cm2, 9.89 J/cm2, 11.1 J/cm2). Atomic force microscope (AFM) phase image and the energy-dispersive spectroscope (EDS) analysis, however, demonstrated that the thermal effects of Er,Cr:YSGG laser with water-cooling spray system on the dentin surface was intense enough to induce notable decrease of the organic matter. Both scanning electron microscopy (SEM) and AFM analysis showed that the irradiated dentine presented rough surface morphology. The surface is clean and dentinal tubules are completely open. The ablation rate of both peri- and intertubular dentine increased at higher energy densities but no significant changes of gross appearance took place. Chemical analysis reveals that laser photothermal effect would decrease significantly the organic content of superficial dentinal layer. We conclude that the Er,Cr:YSGG laser, as a new type clinic laser, would not significantly influence the inorganic phase structure of the surface dentine layer, however, thermal ablation was occurred in organic component. Moreover, the rough ablated surface as well as the opened dentinal tubules induced by irradiation, might be advantageous to the infiltration of the adhesive materials, thus the adhesion of dental restoration could be enhanced. Further studies should focus on the correlation between bond strength and Er,Cr:YSGG lased dentine.

Correlation between the photoluminescence and oriented attachment growth mechanism of CdS quantum dots.

Water-soluble mercaptoacetic acid-coated 3.1 nm CdS quantum dots (QDs) with two concentrations were selected for studying the correlation between the photoluminescence and the crystal growth mechanism. By achieving the classic Ostwald ripening mechanism and oriented attachment (OA) growth mechanism, we have shown that the evolution of the emission spectra were obviously different. The change in both the surface and internal defects during OA crystal growth were responsible for the specific variation of the photoluminescence of CdS QDs. Strategies for obtaining QDs with different luminescent properties are suggested.