Search

The conventional solid-phase sintering method for the preparation of Ln 2 Ti 2 O 7 ceramics using oxides as reactants generally requires higher temperature, larger pressure, and greater energy consumption. In this paper, we synthesize a Eu 2 Ti 2 O 7 ceramic powder in relatively low-temperature molten salt (KCl–NaCl) using Eu 2 O 3 powder and TiO 2 powder as reactants at 1000 °C. The results of XRD, SEM, and element mapping indicate that the product have high phase purity, good crystal morphology and uniform chemical composition. Moreover, Eu 2 Ti 2 O 7 -based glass-ceramics are obtained by sintering with different contents of borosilicate glass. The SEM images of glass-ceramic show that almost no obvious defects or voids are found on the surface of the samples. The values of water absorption for all glass-ceramic waste forms are less than 0.5 %. With the increase of ceramic embedding rate, the hardness of the glass-ceramics first increases and then decreases, while the density gradually increases. When the embedding rate increased to 30 wt%, the hardness of glass-ceramic reaches a maximum of 19.53 GPa. The glass-ceramic waste form embedded with 30 wt% Eu 2 Ti 2 O 7 exhibits very stable chemical durability with a low leaching rate of 1.42 × 10−8 g m−2 d−1 at 90 °C even after 28 days. [ABSTRACT FROM AUTHOR]

The non-uniformity of a single crystal can sometimes be found in biominerals, where surrounding biomacromolecules are incorporated into the growing crystals. This unique composite structure, combining heterogeneity and long-range ordering, enables the functionalization of single crystals. Polymer gel media are often used to prepare composite single crystals, in which the growing crystals incorporate gel networks and form a bi-continuous interpenetrating structure without any disruption to single crystallinity. Moreover, dyes and many kinds of nanoparticles can be occluded into single crystals under the guidance of gel incorporation. On this basis, the bio-inspired method has been applied in crystal morphology control, crystal dyeing, mechanical reinforcement, and organic bulk heterojunction-based optoelectronics. In this paper, the composite structure, the incorporation mechanisms, and the multiple functions of gel-incorporated single crystals are reviewed. [ABSTRACT FROM AUTHOR]

Context: Ammonium perchlorate (NH4ClO4, abbreviated as AP) has the advantages of high oxygen content, high density, and good compatibility, and has significant application prospects in the field of energetic materials. The crystal morphology has a great influence on the properties and sensibility of energetic materials, and a single experimental means is difficult in exploring the crystals; therefore, the crystal morphology of AP is investigated using molecular dynamics simulation complemented with experiments, to theoretically analyze the differences in AP crystal habit and the interactions between solvent molecules and the main growing crystal surfaces of AP. The results show that AP crystal is mainly composed of five independent crystal surfaces (0 0 1), (0 1 0), (1 0 0), (1 0 1), and (1 0 −1) in vacuum using the BFDH laws, with (0 0 1) surface being the main growth crystal surface. In contrast, in H2O solvent, the (1 0 1) and (1 0 −1) surfaces disappear, and the AP mainly consists of (0 0 1), (0 1 0), and (1 0 0) surfaces with a rectangular shape. The crystal morphology obtained from theoretical prediction is in good agreement with that obtained from experimental culture. This paper can provide a new idea for the cultivation and preparation of AP large crystals, and promote the application of AP crystals in energetic materials. Methods: The crystal morphologies of AP in vacuum and H2O solvent under Dreiding force field were predicted based on attachment energy model by using molecular dynamics method in Materials Studio 2019 software. The entire molecular dynamics simulation was carried out under the NTV system, the temperature control method was selected as Anderson, and the system temperature was set to 298 K. The simulation time was set to 40 ps, the step size was set to 1 fs, and the data were outputted every 5000 steps. [ABSTRACT FROM AUTHOR]

Oiling‐out is a common phenomenon in industrial crystallization processes that not only prolongs the total operating time but also leads to undesirable crystal morphology, making it challenging to control crystallization paths. This review provides a comprehensive overview of the oiling‐out phenomenon in organic small molecule crystallization. First, the formation mechanisms of oiling‐out are summarized from both thermodynamic and dynamic perspectives, providing the theoretical foundation for understanding the phenomenon. Then, the universal characterization methods for studying the oiling‐out phenomenon of organic small molecules are introduced in detail, covering both offline and online analytical tools. Moreover, the regulation strategy for oiling‐out, including solvents, impurities, seeding, temperature, and mixing methods are discussed. This paper also focuses on the application of oiling‐out in co‐assembly and crystal shape modulation. Finally, future opportunities and challenges are presented to address the current shortcomings and application bottlenecks in the study of organic small molecule oiling‐out phenomena. This review aims to provide valuable insights and guidance for researchers working on the crystallization of organic small molecules, particularly in the pharmaceutical industry, to better understand, control, and utilize the oiling‐out phenomenon. [ABSTRACT FROM AUTHOR]

In this paper, the melting memory effect generated by a novel cyclic thermal treatment protocol with form II as "seeds" on the polymorphic transformation in isotactic polybutylene-1(iPB-1) was investigated. Polar Optical Microscope (POM), wide angle X-ray diffraction (WAXD) and Fourier transform infrared spectroscopy (FTIR) were used to study the changes of morphology and crystal form II → I transition during aging. Selected crystallization temperature (Tsc) and melting temperature (Tsm) were applied to generate residual nuclei of form II. Both cycled and uncycled samples were analyzed to demonstrate the formation of crystal I and polymorphic transformation. The results indicate that the melting memory has a significant effect on tetragonal modification, leading to an increased nucleation density and an accelerated nucleation speed. The ordered chain sequences in crystal II initiated the formation of crystal nuclei of form I, resulting in a rapid conversion and increased transition degree during the hexagonal crystal growth. Form I was found to have two formation pathways, including the transformation of the unstable crystal form II and the direct formation from residual crystal and melt, which have been rarely discussed before and may shed light on understanding of crystal formation mechanism in polymorphism polybutene-1. [ABSTRACT FROM AUTHOR]

Engineering of organic single crystal toward controllable and aligned patterns at microscale is crucial to the realization of highly integrated organic photonic devices and optoelectronics. However, precise positioning and controllable morphology of crystal structures is still challenging due to the strict conditions for crystal growth. In this paper, a solution based crystal regulation strategy with the assistance of template‐constrained growth method and femtosecond laser processing technology is developed to prepare aligned crystalline microribbon arrays. Simple solvent evaporation results in the random distribution and orientation of self‐assembled crystalline microribbons while it tends to form highly crystalline and orderly microribbon arrays assisted by the confined template microchannels. The large‐scale microribbon array can be fabricated as organic photodetectors with sensitive and fast response under 405 nm illumination. By virtue of the femtosecond laser processing technique, the microribbon arrays are precisely processed into a series of crystal subunits and each microribbon subunit can function as an individual microcavity resonator to produce stable, high‐quality organic laser. The facile solution based template‐constrained self‐assembly and femtosecond laser processing method provide novel strategies to generate highly oriented and controllable crystal structures for the potential applications in integrated organic lasers and optoelectronics. [ABSTRACT FROM AUTHOR]

This paper proposes a technique for producing underground backfilling materials using enzyme-induced calcium carbonate precipitation (EICP) technology to address the growing ecological security concerns caused by coal mining. To augment the mineralization impact of EICP, diverse levels of organic substances, including yeast extract, peptone, and skimmed milk powder, were incorporated into the cementing solution to offer a greater number of nucleation sites for the precipitation of calcium carbonate. The results indicate that (1) based on visual observations, all the sand columns remained intact after cementation, demonstrating a good cementation effect; (2) unconfined compressive strength (UCS) test findings demonstrated that the introduction of organic components effectively augmented the strength of EICP. Among these materials, skimmed milk powder exhibited the most significant effect, resulting in a 66.01% increase in the UCS of EICP at a concentration of 6 g/L. Peptone also showed a positive impact, albeit to a lesser extent, while yeast powder had a relatively lower effect; (3) The utilization of scanning electron microscopy (SEM) revealed a significant diversification in the crystal morphology of calcium carbonate when combined with organic materials through the EICP process. An X-ray diffraction (XRD) test confirmed the presence of calcite and vaterite. This finding implies that the molecular structure of calcium carbonate is enhanced by the inclusion of organic materials. [ABSTRACT FROM AUTHOR]

[Display omitted] • (Ni x Co 3− x)S 4 NPs were synthetized through cation exchange started from spinel Co 3 S 4 NP. • Composition-catalytic activity relation of (Ni x Co 3− x)S 4 NPs were established. • Structural modulation induced by ionic diffusion provided additional active sites. • Disordered structure facilitated continuous phase transformation into Co/NiOOH. • (Ni 1.2 Co 1.8)S 4 NPs with tailored chemical and structural properties enhanced OER activity. Transition metal spinels are promising oxygen evolution reaction (OER) catalysts; however, their rational design has been impeded by their inherent elemental and structural complexities. To alleviate these issues, this paper describes the role of cation exchange in developing active OER catalysts whose chemical and structural features are tailored while their morphology and crystal structure are maintained for enabling a systematic comparison. Through cation exchange, pre-synthesized Co 3 S 4 spinel nanoparticles (NPs) transform into (Ni x Co 3− x)S 4 NPs with compositions ranging from Co-rich to Ni-rich phases. Apart from stoichiometry, the atomic disorder and chemical state of the metal cations are amended through excessive interdiffusion and interstitial site preference of the cations, evidently helping boost the catalytic activity. Specifically, (Ni 1.2 Co 1.8)S 4 —which exhibits an optimal Ni/Co ratio, high structural disorder, and distinct surface chemical states—shows excellent OER performance (overpotential at 10 mA/cm2: 298 mV). In-depth analyses including in situ Raman spectroscopy and DFT calculations indicate that (Ni 1.2 Co 1.8)S 4 gradually transforms into OER-active Co/NiOOH—which has a unique electronic structure with strong reaction-intermediate-adsorbing characteristics—during the OER cycles. Overall, the study findings underscore the potency of cation exchange as a tool for controlling structural and chemical features, thereby helping explore complex catalyst materials while enhancing their activity. [ABSTRACT FROM AUTHOR]

Protein retarders can not only prolong the setting time of gypsum in application, but also lower the reduction in strength. The chemical activity of proteins is determined by the basic unit of amino acids (AAs). To enhance the understanding of protein retarding action mechanism, this paper focuses on the AAs-adsorbed gypsum structure, and investigated the retarding effects, crystal morphologies, and nanoscale interactions. Results indicate that the AAs had varying retarding effects on gypsum, and the effects from greatest to smallest were L-arginine, L-glutamic, and L-leucine acid. The rate of initial hydration heat release was reduced, and the peak of hydration release was delayed. Retardation of AAs on gypsum involves chemical adsorption on the surface of dihydrate gypsum crystals, which mainly occurs on the (1 2 0) face and affect gypsum morphology. The mechanism of AAs adsorption involves electrostatic interactions between charged functional groups of AAs and gypsum particles, as well as hydrogen bonding at additional carboxyl and amino groups. The adsorption strength depends on longer chained structure and number of functional groups of the AAs. And intrinsic strength of AAs-adsorbed gypsum nanocrystals contributes to the strength reduction on the macroscale. This paper provides basic data for designing and tailoring enhanced protein retarders for gypsum. • The amino acids adsorbed gypsum mechanism was revealed to evaluate protein retarding effects. • Retardation of AAs on dihydrate gypsum crystals mainly occurs on the (1 2 0) face. • Intrinsic strength of AAs-adsorbed gypsum nanocrystals contributes to the strength reduction on the macroscale. • Electrostatic interactions and hydrogen bonding determine the AAs adsorption effects. [ABSTRACT FROM AUTHOR]

• NiFe 2 O 4 was prepared by a thermal decomposition process with various temperatures. • The micro-octahedral NiFe 2 O 4 grows along the dissolution‑recrystallization. • The FT-IR bands reveal the cation shifting from octahedral to tetrahedral structure. • The Eg (1.67 and 1.57 eV for 900 and 1,000 °C heating) refers 3A2g(3F) → 3T1g(3F). In this paper, NiFe 2 O 4 powders were prepared by a thermal decomposition process with various temperatures. The structural characteristic and intrinsic defect were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, ultraviolet–visible (UV–vis) spectroscopy, and photoluminescence (PL). The morphology was investigated by scanning electron microscope (SEM) and transmission electron microscope (TEM). XRD pattern reveals the pure NiFe 2 O 4 phase as the calcination temperature of 900 and 1,000 °C. The calcination of 900 °C depicted the micro-octahedral structures with a smooth surface. The calculated hopping length and the FT-IR spectra reveal the cation shifting from octahedral to tetrahedral structure. The decreasing energy bandgap of NiFe 2 O 4 was investigated as the calcination temperature increased. The PL transition of 3A2g(3F) → 3T1g(3F) refers to the band-to-band emission. The structural characteristics, morphology, and defects were investigated and discussed in terms of phase, bonding vibration, crystal growth mechanism, emerging energy level and electron transition. [ABSTRACT FROM AUTHOR]

The Organic–inorganic hybrid compounds have attracted considerable attention for their scientific and technological potential according to their wide field application. In this paper, we describe the preparation of a new hybrid crystal, with the structural formula [C 6 H 9 N 2 ] 2 SnCl 6 , of which crystallographic, BFDH morphology, Hirshfeld and complex impedance spectroscopy have been studied and analyzed. The X-ray diffraction analysis revealed that the title compound crystallized in the centrosymmetric space group P2 1 /c of the monoclinic system. The powder XRD is used to confirm the phase purity of the sample and the crystalline nature of the powder. The [C 6 H 9 N 2 ] 2 SnCl 6 crystal morphologies are simulated from the Laue symmetry (2/m), and from the space group symmetry (P2 1 /c), which highlighted the effect of the screw axe 2 1 and the glide plane c in reducing the Importance morphology in the constructed model considering the space group symmetry. The intermolecular interactions studied using Hirshfeld surfaces showed the important contribution of H⋯Cl/Cl⋯H intercontacts (67.1 %) in the [C 6 H 9 N 2 ] 2 SnCl 6 crystal packing. The analysis of real and imaginary parts impedance spectra shows that the electrical properties are heavily dependent on frequency and temperature, indicating a relaxation phenomenon and semiconductor-type behavior. The Nyquist plot (-Z″ vs Z′) showed only one semicircular arc, representing the grain effect in the electrical conduction. The obtained results were analyzed by fitting the experimental data to an equivalent circuit model R/CPE/C. The Alternating current conductivity (σ AC) follows Jonscher's power law. The latter confirmed that the conduction is insured by the non-overlapping small polaron tunneling model (NSPT) model, which has been studied in depth. [ABSTRACT FROM AUTHOR]

Clay is a rich aluminosilicate resource with unique advantages as a raw material for zeolites production. However, synthesizing nanosized single-crystalline zeolites through a simple approach using clay remains a significant challenge. In this paper, acid-washed montmorillonite (MSR) was used to prepare nano-H-ZSM-5 single crystals with high crystallinity, uniform grain size and permeable straight pores under the induction of a small amount of organic template tetrapropylammonium hydroxide (TPAOH). Through temperature-staged treatment, the nucleation and growth process of zeolite were decoupled, ultimately achieving precise control over the size of the nano-single crystals. Mechanistic study showed that the low-temperature aging process produces smaller structural units which probably derived from the geopolymer topology of the clay, providing more active sites for zeolite nucleation, leading to the rapid crystallization during the high-temperature process. The porous structure promotes material diffusion, inhibits aromatic cycling and reduces carbon formation in the pores. The large specific surface area and nanoscale multilayer pore structure delay carbon accumulation and increase carbon holding capacity. These properties make nano-ZSM-5 single crystals an excellent choice for high olefin selectivity and long catalytic life in the methanol-to-olefin reaction. This synthetic route provides a general strategy for preparing nanosized zeolite single crystals from clay. [Display omitted] • High-quality nano-ZSM-5 single crystals with uniform morphology and good dispersion was obtained. • Nano-zeolite size can be precisely controlled by decoupling the nucleation and growth processes. • The "homogeneous silica–alumina" property of montmorillonite was crucial for ZSM-5 synthesis. • Nano-H-ZSM-5 has uniformly dispersed acid sites and effectively catalyzed the MTO reaction. • A general strategy broadens the idea for the application of clay in the field of zeolite synthesis. [ABSTRACT FROM AUTHOR]

BFDH crystal model morphology/stereoscopic projection, experimental (•••) calculated (—), and difference profile (—) of XRD pattern, and crystal structure of (CH 3) 4 N] 3 Bi 2 Cl 9. [Display omitted] The present paper reports on synthesis method, X-ray diffraction, DSC, Infrared and Raman spectroscopy studies carried out on [(CH 3) 4 N] 3 Bi 2 Cl 9. The structure of this hybrid material is refined by the Reitveld method in the space group P 6 3 / mmc (Z = 2), with unit cell parameters: a = 9.2581(2) Å, c = 21.9223(6) Å, V = 1627(1) Å3. It consists from isolated Bi 2 Cl 9 3- dimer anions composed of two distorted octahedra BiCl 6 3- sharing three chlorine atoms' face, and three disordered cations (CH 3) 4 N+, forming an organic–inorganic network. There are two disordered cations types: one cation totally disordered with N(1) atom placed in special Wyckoff positions (2b) of (-6m2) site symmetry, and Carbon atoms C1 and C 2 are three-fold disordered; the two others cations N(2) observed on special positions (4f) of site symmetry (3 m) are partially disordered, with C4 atom is three-fold disordered and C3 atom is ordered. The BFDH crystal morphology predicted from the Laue symmetry (6/mmm) gives hight faces characterized by two faces indices, with their center-to-plane distance d hkl and their growth rates. The simulated model from the space group symmetry (P 6 3 / mmc) gives three < h k l > faces indices, which highlights the screw axis 6 3 and the glide plane c effects in reducing the Importance morphology. The DSC analysis showed that the compound undergoes a reversible phase transition at 74 °C/69 °C (heating/cooling). The Infrared-Raman spectra are studied based by developing theoretical vibrations modes of cations and anions in the crystal; the study confirms the presence of (CH 3) 4 N+ cations and Bi 2 Cl 9 3- anions, which are linked by C H....Cl hydrogen bonding types. [ABSTRACT FROM AUTHOR]

1. Synthetic route of copolymer. 2. Possible mechanism of (C16-AM, C16-IM and C16-SM) for improving the fluidity of diesel oil at low temperature. [Display omitted] • Comb-like PAOs were synthesized from long-chain olefin and benzene containing olefin. • Comb-like PAOs can effectively improve the low temperature cold flow of diesel fuel. • The properties of synthetic PAOs and commercial PPDs were compared during oxidation. • The crystallization behaviors of Comb-like PAOs were studied. Pour point depressants (PPDs) represent an efficient and economical approach to enhance diesel's low-temperature fluidity, yet their efficacy is influenced by molecular structure and surfactant moieties. To achieve highly effective PPDs, a series of comb-structured poly-alpha-olefins (PAOs) were synthesized in this paper, designated as 1-hexadecene-styrene (C16-SM), 1-hexadecene- allyl benzene (C16-AM), and 1-hexadecene-indene (C16-IM). The copolymers' impact on diminishing diesel's solid point (SP) and cold filter plugging point (CFPP) was thoroughly investigated. Notably, with a 1-hexadecene to styrene monomer molar ratio of 20:1, the most favorable inhibitory effect of C16-SM was observed, exhibiting a reduction of 10 °C for CFPP and 30 °C for SP. Comparing C16-SM to commercial pour point depressants (CPPDs) after subjecting them to an accelerated oxidation test revealed that the C16-SM performance was more stable under oxidative conditions. To address stability and environmental pollution concerns associated with PPDs, this study aims to develop a stable, eco-friendly PAO PPD and assess the influence of various benzene ring-based monomers on diesel's cold fluidity in low-temperature conditions. Furthermore, a novel mechanism elucidating the change in crystal morphology and size by PAOs is proposed. [ABSTRACT FROM AUTHOR]

For further energy enhancement of water-reactive metal fuels, it is crucial to find aluminum composites that can react synchronously and quickly with multiple types of water (ice, steam, and water). In this paper, two graphite-based aluminum composites, aluminum/bismuth/graphite (Al/Bi/GI) and aluminum/bismuth/graphene nanosheets (Al/Bi/GE), were prepared. The morphology and crystal structure of the composites were characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The reactivity of Al/Bi/GI and Al/Bi/GE with water from 20 °C to 80 °C and ice at 0 °C and −15 °C was characterized using hydrogen generation properties. Their ignition and combustion properties in high-temperature water steam from 300 °C to 900 °C were also investigated. The results show that Al/Bi/GI and Al/Bi/GE composites prepared by ball milling have blocky and multilayered lamellar structures, respectively. That ball milling does not result in the formation of new alloys. The thickness of graphite material affects the reactivity of activated aluminum composites. The hydrogen generation rates of Al/Bi/GE in water and ice are much higher than that of Al/Bi/GI. The maximum hydrogen generation rates of Al/Bi/GE were 28.8 and 46.6 times higher than those of Al/Bi/GI in water at 20 °C and ice at −15 °C, respectively. In high-temperature water steam, the ignition temperature and ignition delay time of Al/Bi/GE are lower than those of Al/Bi/GI. Al/Bi/GE achieves a rapid reaction that can be synchronized with three forms of water and is expected to be applied to water-reactive metal fuel propellants. • Al/Bi/GI and Al/Bi/GE composites with different structures were prepared. • The multilayered lamellar structure of Al/Bi/GE has superior synergistic reactivity with different forms of water. • The MHGR of Al/Bi/GE on ice at −15 °C is 12.6 mL‧g-1‧s-1, 46.6 times higher than that of Al/Bi/GI. • Al/Bi/GE exhibits better combustion performance in high-temperature steam. [ABSTRACT FROM AUTHOR]

This paper reports the synthesis, structure, BFDH crystal morphology, Raman and Infrared spectroscopic studies of three novel metal orthophosphate salts MII(Ga 0.5 Sb 0.5)(PO 4) 2 (MII= Sr, Pb, Ba), abbreviated [Sr], [Pb], [Ba]. The structures of these phases are refined from X-ray powder diffraction data by the Rietveld method. The yavapaiite [Ba] phase is monoclinic of C2/m space group [Z=2; a= 8.106(4) Å; b= 5.178(3) Å c= 7.806(1) Å, β=94.79(4)°, V= 327(1) Å3]. Its structure consists of layers, running along the (a, b) plane, and built up of corner-connected Ga(Sb)O 6 octahedra and PO 4 3− tetrahedra. The two isotypic phases [Sr]/[Pb] of distorted yavapaiite structure crystallize in the monoclinic C2/c space group (Z=4) with parameters: a=16.455(4)/16.622(7) Å; b=5.158(1)/5.163(2) Å c= 8.005(1)/8.067(3) Å; β=115.49(1)/114.85(2)°, V= 613(1)/628(5) Å3. Their structures consist of MO 10 (M= Sr, Pb), PO 4 3− tetrahedra and Sb(Ga)O 6 octahedra. In [Pb] phase, the Pb is surrounded by eight oxygen atoms (Pb-O: 2.65-2.77 Å) and two oxygen atoms forming abnormal bond distances Pb-O(4) [3.447(3)Å]. The BFDH crystal morphology predicts hight (h k l) facets for each compound, the center-to-plane distances d hkl are slightly strong in the distorted Yavapaiite [Pb/Sr] rather than in [Ba]. The IR and Raman study is performed based on theoretical group analysis considering C s site symmetry of PO 4 3− groups in [Ba], and C i symmetry in [Pb]/[Sr] phases. The assignment and discussion of the observed bands were done by comparison with other yavapaiite materials. The UV–visible investigation reveals direct optical gap energies of values 4.16 eV for [Ba] and 4.24 eV for [Sr], indicating a semi-conducting nature of the prepared materials. Crystal structures, UV absorbance, and and Tauc Plots (F(R)hν)1/2 of versus hν of AII(Sb 0.5 Fe 0.5)(PO 4) 2 (AII = Ba, Pb, Sr) compounds. [Display omitted] • Novel A(Sb 0.5 Ga 0.5)(PO 4) 2 (A= Ba, Pb, Sr) crystal structures are determined and discussed. • The BFDH morphology of [Ba] and [Sr] are simulated from parametres and Laue symmetry of these crystals. • Theoretical analyses are made in assignment of IR and Raman bands for the three phases. • UV–visible absorptions indicate a semi-conducting nature of the synthetised materials. [ABSTRACT FROM AUTHOR]

Cuprous oxide (Cu2O) nano- and microstructures possess unique properties that may find a variety of applications. Environmentally benign synthesis of Cu2O with well-controlled morphology is highly desirable. In this study, Cu2O crystals with tunable shapes are synthesized using cellulose nanofibrils (CNFs) as a shape regulator and the sole reducing agent in aqueous environment. By simply increasing Cu2O precursor concentration, the Cu2O crystals evolved from octahedra to cuboctahedra, and finally cubes, accompanied with increasing size from nano- to microscale. The selection of Cu chelating agent (sodium tartrate or potassium sodium tartrate) affected the crystal growth rate. Transition in the relative intensities of the (111) and the (200) crystalline peaks in their XRD patterns was consistent with the morphology change. During the growth of crystals, CNFs were preferably bound to the {111} crystalline facet. The introduction of KBr to the reaction system produced short hexapods. The resultant CNF-Cu2O hybrids were incorporated into waterborne polyurethane (WPU) films. Even with 0.5 wt% CNF-Cu2O, the WPU film showed significant enhancement in modulus, strength and elongation at break. This work proves the possibility of controlled growth of Cu2O particles aided by CNFs and provides a new strategy for improving the performance of eco-friendly WPU films. [ABSTRACT FROM AUTHOR]

• Acrylamide can neutralize the acidity of the hole-transport layer. • Acrylamide can optimize the quality of the FASnI 3 perovskite film. • The efficiency of FASnI 3 perovskite solar cells is increased by almost 46 %. The quality of the hole transport layer (HTL) is crucial for the overall efficiency of the perovskite solar cells. Although poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonic acid) (PEDOT:PSS) has been widely used as HTL for the perovskite solar cells, there is still room for further improvement of PEDOT:PSS by optimizing its energy level matching and the hole transfer efficiency. Based on the present issues of applying PEDOT:PSS as HTL in tin-based perovskite solar cells, the Lewis alkali acrylamide (AM), which contains both carbon-carbon double bond and the electrophilic amide group, is applied as the dopant in PEDOT:PSS solution. By analyzing the surface morphology and the crystal structure, it is revealed that AM can effectively improve both the quality and crystallinity of the formamidinium tin tri-iodide (FASnI 3) perovskite film, with the defects of the perovskite film greatly suppressed. The grain size of the modified FASnI 3 perovskite is observed to increase with the surface roughness reducing at the same time, along with the charge recombination resistance of the FASnI 3 perovskite film increasing. As a result, the modified devices have a higher short-circuit current, fill factor as well as power conversion efficiency. The characterization of the surface contact angle indicates that a more hydrophobic surface is formed as for the FASnI 3 perovskite film, which could efficiently retard the ambient vapor penetrating into the perovskite film. [ABSTRACT FROM AUTHOR]