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JOURNAL OF THE EUROPEAN CERAMIC SOCIETY · 2021 · IF 5.302

Influence of tricalcium aluminate on the microstructure evolution of CaO specimen during hydration

Bingrong Li,Yaowu Wei,Junfeng Chen,Nan Li

C 3 A-containing CaO specimen was prepared and the evolution of its microstructure during hydration process was investigated to clarify the protective mechanism of tricalcium aluminate (C 3 A) on hydration resistance of CaO specimen. The slit-shaped micropores were formed on the grain boundary of CaO due to the stacking of lamellar C 4 AH 13 formed by the hydration of C 3 A. The contact area of residual C 3 A with the moisture was reduced by the porous C 4 AH 13 layer at the original site, which resulted in a slower dissolution rate of C 3 A grain through the porous layer. In addition, the crack propagation and the formation of macropores were inhibited by the pinning effect of C 4 AH 13 , which was beneficial to the improvement of hydration resistance.

CAS / MDL: 1344-28-1 471-34-1
研究领域: 材料科学 · 化学工程
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CORROSION SCIENCE · 2022 · IF 7.72

A robust calcium carbonate (CaCO3) coating on biomedical MgZnCa alloy for promising corrosion protection

Pingli Jiang,Ruiqing Hou,Shijie Zhu,Shaokang Guan

To improve the anti-corrosion property of biodegradable magnesium alloy , a CaCO 3 coating was developed by hydrothermal treatment . The prepared coatings generally consisted of three layers: a dark inner layer, a bright middle dense calcite layer and a bright outer loosely deposited CaCO 3 layer. As the electrolyte concentration increased, the formation of the inner product layer and the deposition of loose aragonite products were considerably inhibited, whereas the middle calcite layer became more intact and compact, which conferred enhanced corrosion protection upon the coated samples. Additionally, this coating showed a possible transformation into calcium phosphate during immersion.

研究领域: 材料科学 · 生物医学工程
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Maximizing the utilization of Calcium species in the supercages of CaNa-FAU zeolite for efficient CO2 capture

Xinyu Sun,Quanqi Zhang,Sihan Li,Yiming Zhang,Meiyu Liu,Binbin He,Yi Mei,Yun Zu

Ca-FAU zeolite sorbents have been recognized as one of promising CO 2 capture materials, while it is subject to the change in the speciations and locations of Ca 2+ species as adsorption sites in the FAU zeolite due to its susceptible migration. In this paper, a facile strategy is reported by tuning calcination temperatures and Ca loadings, to maximize the utilization of Ca 2+ species in the supercages of CaNaX zeolites. Detail characterizations of TG-MS, in situ FTIR spectroscopy and XRD Rietveld refinement reveal the changeable regular in the chemical speciations, locations and number of Ca 2+ species in the CaNaX zeolites. Synthetic 0.05CaNaX-250 zeolite (calcined at 250 °C and Ca loading of 1.58 wt%) guarantees at least 21 Ca(OH) + species (depicted as hydroxylated Ca 2+ species) in the supercages per FAU cell unit, close to theoretical value. Such sorbent apparently improves the CO 2 uptakes and the separation from CO 2 /N 2 and CO 2 /CH 4 , along with fast kinetics, low heat of adsorption, measured by dynamic and gravimetric adsorption methods, respectively. In addition, it keeps a superior recyclability after 10 times regeneration. CO 2 -dosing FTIR experiments further illustrate that excellent CO 2 adsorption performance are benefited from the formation of Ca(OH) + ∙∙∙(CO 2 ) 2 adducts with an appropriate interaction. This work is of great significance to better understand the role of cations in FAU zeolites, and also provides an important reference value for the directional design of effective adsorption sites in other excellent CO 2 zeolite sorbents.

研究领域: 材料科学 · 环境科学
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ADVANCED FUNCTIONAL MATERIALS · 2020 ·Vol. 30 ·期 12 ·1909972 · IF 16.836

Controlled n-Doping in Air-Stable CsPbI2Br Perovskite Solar Cells with a Record Efficiency of 16.79%

Yu Han,Huan Zhao,Chenyang Duan,Shaomin Yang,Zhou Yang,Zhike Liu,Shengzhong (Frank) Liu

Cesium-based inorganic perovskites, such as CsPbI 2 Br, are promising candidates for photovoltaic applications owing to their exceptional optoelectronic properties and outstanding thermal stability. However, the power conversion efficiency of CsPbI 2 Br perovskite solar cells (PSCs) is still lower than those of hybrid PSCs and inorganic CsPbI 3 PSCs. In this work, passivation and n-type doping by adding CaCl 2 to CsPbI 2 Br is demonstrated. The crystallinity of the CsPbI 2 Br perovskite film is enhanced, and the trap density is suppressed after adding CaCl 2 . In addition, the Fermi level of the CsPbI 2 Br is changed by the added CaCl 2 to show heavy n-type doping. As a result, the optimized CsPbI 2 Br PSC shows a highest open circuit voltage of 1.32 V and a record efficiency of 16.79%. Meanwhile, high air stability is demonstrated for a CsPbI 2 Br PSC with 90% of the initial efficiency remaining after more than 1000 h aging in air.

研究领域: 材料科学 · 光伏技术 · 能源研究
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SEPARATION AND PURIFICATION TECHNOLOGY · 2018 · IF 3.927

Separation of scheelite and calcite using calcium lignosulphonate as depressant

Bo Feng,Wei Guo,Jinxiu Peng,Wenpu Zhang

The flotation separation of scheelite and calcite by froth flotation is difficulty as these two minerals have similar physicochemical characteristics. To solve this problem, the role of calcium lignosulphonate (CLS) in the flotation separation of scheelite from calcite has been studied and the separation mechanism has been discussed. The micro-flotation tests show that calcium lignosulphonate has strong depression effect to calcite and the depression effect decreased with the increase in pH. However, its depressive effect to scheelite is weak at pH 6–9. A concentrate with WO 3 grade of 65.02%, and WO 3   recovery of 79.64% was achieved in the flotation separation of mixed mineral, while calcium lignosulphonate was used. The reason is that the adsorption amount of calcium lignosulphonate on scheelite surface is far less than that of calcite according to adsorption tests. The interaction mechanism of calcite and CLS was studied by XPS and the results shows that the interaction between calcite and CLS were chemisorptions, and this interaction that SO 3 group were involved hindered the absorption between Ol − and the Ca 2+ on the surface of calcite, it also shows that a small amount of Ca(OH) 2 was generated on the surface of calcite in the presence of CLS, the coefficient of these two mechanisms brings about the depression effect for calcite.

CAS / MDL: 8061-52-7 143-19-1
研究领域: 矿物加工工程 · 化学工程
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MOLECULES · 2022 ·Vol. 27 ·期 6 ·1828 · IF 4.927

Unveiling the Effect of Solvents on Crystallization and Morphology of 2D Perovskite in Solvent-Assisted Method

Yingjie Su,Jianqiang Xue,Anmin Liu,Tingli Ma,Liguo Gao

Controlling the crystallographic orientations of 2D perovskite is regarded as an effective way to improve the efficiency of PSCs based on 2D perovskite. In this paper, five different assistant solvents were selected to unveil the effect of solvents on crystallization and morphology of 2D perovskite in a solvent-assisted method. Results demonstrated that the effect of Lewis basicity on the crystallization process was the most important factor for preparing 2D perovskite. The stability of the intermediate, reacted between the solvent and the Pb2+, determined the quality of 2D film. The stronger the Lewis basicity was, the more obvious the accurate control effect on the top-down crystallization process of 2D perovskite would be. This could enhance the crystallographic orientation of 2D perovskite. The effect of Lewis basicity played a more important role than other properties of the solvent, such as boiling point and polarity.Keywords:2D perovskite;perovskite solar cells;crystallization orientation;solvent

研究领域: 材料科学 · 化学工程
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Thick film high-performance carbon-based CsPbIBr2 perovskite solar cells vis nano-perovskite modified hot casting method

Zhenbo Du,Yuan Xu,Yu Jing,Ruoshui Li,Jianming Lin,Jihuai Wu,Zhang Lan

All-inorganic carbon-based CsPbIBr 2 perovskite solar cells (PSCs) have attracted attention due to their more balanced performance and stability. The performance of the PSCs is highly dependent on the quality of the absorber films. Unfortunately, most high-performance films are prepared in a glove box and conventional preparation methods often produce perovskite films within 400 nm of thickness, which is detrimental to large area device fabrication and limits their commercial application. Here we had demonstrated a short chain ligands nano-CsPbIBr 2 particles modified hot-casting method to deposit a perovskite film with thickness up to 800 nm. It was carried out by spin-coating a hot CsPbIBr 2 precursor solution onto nano-CsPbIBr 2 particles film on an electron transport layer (ETL), and then depositing nano-CsPbIBr 2 particles on the precursor film again before annealing. The nano-CsPbIBr 2 particles on the ETL promotes precursor solution crystallization and increased film thickness, and the nano-CsPbIBr 2 particles on the precursor film promoted grain growth and reduced defects due to compositional deviations from stoichiometric ratios. The power conversion efficiency (PCE) of the PSCs fabricated by this method is up to 10.66 %. The unencapsulated PSCs still retain more than 85 % of the initial PCE when stored at ambient atmosphere (RH 50–60 %) for 10 days.

研究领域: 材料科学 · 太阳能 · 纳米技术 · 化学工程
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CERAMICS INTERNATIONAL · 2025 · IF 5.6

Research on the sintering temperature and absorptivity of corundum-based endothermic ceramics for solar thermal power generation

Jianfeng Wu,Xinxin Shi,Shaoheng Liu,Xiaohong Xu,Yaqiang Shen,Deng Zhang

The absorptivity of endothermic materials serves as a critical index for solar thermal power photothermal conversion systems, and ceramic-based endothermic materials characterized by high absorptivity also exhibit elevated sintering temperatures. In this study, CaF 2 was employed as an additive to investigate its effects on the physical properties and microstructure of the samples, with a particular focus on the mechanism by which CaF 2 reduces the sintering temperature of corundum-based endothermic ceramics. The results showed that the G2 sample (1 wt% CaF 2 ), sintered at 1650 °C, displayed the best physical properties, including 93 % absorptivity, 165.43 MPa bending strength. The sintering temperature of the CaF 2 -doped G-series samples was around 60 °C lower due to liquid-phase calcium hexaaluminate formation from CaF 2 and Al 2 O 3 , which enhanced atomic migration and facilitated ceramic matrix sintering. Additionally, the capillary forces of the liquid-phase calcium hexaaluminate promoted ceramic matrix shrinkage and accelerated corundum-based grain growth through the dissolution-precipitation mechanism, leading to densification. Moreover, the G2 sample exhibited excellent durability, with absorptivity decreasing by only 1.9 % after 100 h at 1000 °C.

CAS / MDL: 1309-37-1
研究领域: 材料科学 · 太阳能技术
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 40 · IF 1.768

Drug-loaded microparticles prepared by the one-step deposition of calcium carbonate/alginate onto cotton fabrics

Huan-Ling Wu,Xiao-Xiao Hou,Christopher Branford-White,Xiao-Zhu Sun,Lei Tao,Syeda Um-I-Zahra,Li-Min Zhu

Calcium carbonate (CaCO 3 )/alginate inorganic–organic hybrid particles were synthesized and deposited on to the surface of cotton fabrics with a novel one-step procedure. The effects of the Ca 2+ /CO 3 2− /alginate molar ratio on the cotton matrix were investigated. The optimization of the process resulted in a regular shaped hybrid microparticles, and scanning electron microscopy revealed that the particles were uniformly distributed on the surface of the fibers. Dynamic light scattering showed that the particles were about 2 μm in diameter. Moreover, transmission electron microscopy images demonstrated that the core–shell structure of the particles existed along with CaCO 3 evenly enfolded into the alginate layer. An X-ray diffraction pattern displayed that the alginate/CaCO 3 hybrid microparticles were a mixture of calcite and vaterite crystal. Fourier transform infrared spectroscopy indicated that CaCO 3 /alginate hybrid particles formed in situ were the only deposited materials. The thermogravimetric analysis curve indicated a certain mass ratio of the alginate and CaCO 3 in the hybrid particles. Furthermore, the drug-loading and drug-release properties of the hybrid microspheres were studied, and the results show that the water-soluble diclofenac sodium could be effectively loaded in the hybrid microparticles and the drug release could be effectively sustained. Finally, both of the microparticles and modified fabrics had good cytocompatibility. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42618.

研究领域: 材料科学 · 生物医学工程 · 纺织科学
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Small · 2020 ·Vol. 16 ·期 25 ·2001551 · IF 11.459

Eu3+, Sm3+ Deep-Red Phosphors as Novel Materials for White Light-Emitting Diodes and Simultaneous Performance Enhancement of Organic–Inorganic Perovskite Solar Cells

Shahid Ullah Khan,Waheed Ullah Khan,Wasim Ullah Khan,Dilfaraz Khan,Sumbul Saeed,Syed Badshah,Muhammad Ikram,Tawfik A. Saleh

The luminous efficiency of inorganic white light-emitting diodes, to be used by the next generation as light initiators, is continuously progressing and is an emerging interest for researchers. However, low color-rendering index (Ra), high correlated color temperature (CCT), and poor stability limit its wider application. Herein, it is reported that Sm 3+ - and Eu 3+ -doped calcium scandate (CaSc 2 O 4 (CSO)) are an emerging deep-red-emitting material with promising light absorption, enhanced emission properties, and excellent thermal stability that make it a promising candidate with potential applications in emission display, solid-state white lighting, and the device performance of perovskite solar cells (PSCs). The average crystal structures of Sm 3+ -doped CSO are studied by synchrotron X-ray data that correspond to an extremely rigid host structure. Samarium ion is incorporated as a sensitizer that enhances the emission intensity up to 30%, with a high color purity of 88.9% with a 6% increment. The impacts of hosting the sensitizer are studied by quantifying the lifetime curves. The CaSc 2 O 4 :0.15Eu 3+ ,0.03Sm 3+ phosphor offers significant resistance to thermal quenching. The incorporation of lanthanide ion-doped phosphors CSOE into PSCs is investigated along with their potential applications. The CSOE-coated PSCs devices exhibit a high current density and a high power conversion efficiency (15.96%) when compared to the uncoated control devices.

研究领域: 材料科学 · 光学 · 能源科学
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Nanoscale · 2021 ·Vol. 13 ·期 35 ·14915-14924 · IF 7.79

Enhanced photovoltage and stability of perovskite photovoltaics enabled by a cyclohexylmethylammonium iodide-based 2D perovskite passivation layer

Weihai Sun,Jinjun Zou,Xiaobing Wang,Shibo Wang,Yitian Du,Fengxian Cao,Lan Zhang,Jihuai Wu,Peng Gao

Regardless of the impressive progress that perovskite solar cells (PSCs) have achieved, especially considering their power conversion efficiency (PCE) over 25%, traditional PSCs still contend with an inherent instability with exposure to humidity, which remains as a critical issue for the realization of commercial production. Herein, we proposed an effective pathway to relieve the instability of PSCs without sacrificing efficiency by introducing a 2D phase at the surface of the 3D perovskite film, based on a novel organic cyclohexylmethylammonium iodide (CMAI). The self-assembled thin 2D capping layer atop the 3D perovskite layer can not only reduce the ionic defects, but also serve as a protective barrier against moisture. Consequently, the champion device incorporating 2D perovskite capping layers delivered an open-circuit voltage (Voc) of 1.19 V, which contributes to an impressive PCE of 22.06% on account of the improved charge extraction and decreased non-radiative recombination. More importantly, an excellent long-term stability along with mitigated hysteresis was observed for the modified devices as a result of the suppressed ion migration and high humidity resistance of the 2D perovskite film. Our finding provides a comprehensive approach for simultaneously enhancing the efficiency and stability of PSCs through dimension engineering utilizing CMA-based 2D perovskite materials.

研究领域: 材料科学 · 能源技术
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International Journal of Minerals Metallurgy and Materials · 2020 ·Vol. 27 ·期 9 ·1216-1225 · IF 1.713

Diffusion coefficient of Ti4+ in calcium ferrite/calcium titanate diffusion couple

Wei Wang,Yue Hong-rui,Xue Xiang-xin

This study investigated the interdiffusion of calcium ferrite/calcium titanate system in the time range of 0–120 min by the diffusion couple method in a CO/N 2 reducing atmosphere at 700°C. The results show that after the diffusion reaction occurred, no longitudinal agglomerations were present on the substrate surface on the calcium titanate side. When the diffusion time was increased to 105 min, a net vacancy flow from calcium titanate to calcium ferrite might have occurred, causing the surface of the calcium ferrite substrate to collapse. The thickness of the diffusion layer of the calcium ferrite/calcium titanate system was about 17–48 µm, which conforms to the parabolic law of diffusion. The diffusion coefficient and the Ti 4+ concentration in the calcium ferrite/calcium titanate system are related. This shows an increase in the diffusion coefficient with the increase of Ti 4+ concentration, and the diffusion coefficient value was in the range of 10 −12 –10 −11 cm 2 ·s −1 .

CAS / MDL: 12049-50-2
研究领域: 材料科学 · 化学工程
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