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PROPELLANTS EXPLOSIVES PYROTECHNICS · 2021 ·Vol. 46 ·期 9 ·1480-1488 · IF 1.887

Construction of a Novel Barium-Free Green-Light Emitting Illuminant Based on Boron Carbide

Zhiping Huang,Shengliang Xu,Xinli Chen,Min Wang,Hua Yuan,Huali Zhao,Yuanyuan Zhang

Green-light emitting illuminant and green pearls that are currently being used for pyrotechnics are mainly composed of barium carbonate and polyvinyl chloride (PVC), which lead inevitably to the substantial generation of abundant harmful products for environmental pollution. There is thus considerable scope for the development of a novel emitting illuminant with an improved “green” composition instead of compositions incorporating barium based oxidants and polyvinyl chloride for environmental protection. For this purpose, a new composition composed of boron carbide, potassium perchlorate, and guanidine nitrate with a suitable burning rate of 5∼15 mm/s required for fireworks, the high luminous intensity of 34665 Cd and spectral purity of 67.1 % at a primary wavelength of 562 nm was developed. Notably, PM10 data demonstrated that the new composition generated less than half the amount of the smoke relative to the original one. More importantly, all of the safety parameters of this new formulation meet well with the standards’ requirements, i. e ., a remarkable low sensitivity to friction (0 %) and impact (8 %), relative stability to electric discharge (374.4 mJ), flame (14.0 cm) and heating (unburned, unexploded at 75 °C for 48 h), as well as a high ignition temperature of 504.0 °C and a low moisture absorption rate (0.66 %). Taken together, the new emitting illuminant developed herein showed great potential to be used for fireworks and signal flare in both military and civilian applications.

CAS / MDL: 100-97-0
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ACS Applied Nano Materials · 2021 · IF 5.097

Multicolor Graphene Quantum Dots via Solvatochromic Tuning and Sulfur Doping for Light-Emitting Diodes

Yongsheng Yang,Changxing Wang,Siyuan Tang,Da Chen,Xiameng Li,Zhao Peng,Chenjie Gu

Recently, graphene quantum dots (GQDs) with polychrome emission capability have attracted much attention due to their multifarious applications. In this study, we report a facile and green approach for rapid preparation of multicolor emission GQDs. Experimentally, UV light was used to drive the low-temperature synthesis, and a tunable emission wavelength of the GQDs was achieved through the synergistic effect of solvatochromic tuning and sulfur doping. Results show that multicolor emission wavelengths of green-GQDs (G-GQDs) from blue to yellow are obtained by simply controlling the polarity of the surrounding solutions. Moreover, red-GQDs with the emission wavelengths extended from green to red are further obtained by sulfur doping. Thereafter, G-GQDs were used to develop a trace water-detecting platform, ascribed to the high sensitivity of water-quenchable fluorescence, and a low detection limit of 0.061% was achieved. Meanwhile, based on the outstanding multicolor tunability of as-prepared GQDs, we successfully manufactured multicolor solid fluorescence films to fabricate multicolor light-emitting diode (LED) devices. Furthermore, high-quality white LEDs (WLEDs) are fabricated with the CIE coordinates of (0.341, 0.354) and a color temperature of 5161 K. This study highlights the potential of GQDs in various applications, including solid-state fluorescence films, optoelectronics, and optical molecular sensing.

CAS / MDL: 120-80-9 95-54-5
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ENVIRONMENTAL RESEARCH · 2021 · IF 6.498

Dual light-driven p-ZnFe2O4/n-TiO2 catalyst: Benzene-breaking reaction for malachite green

Jiayi Li,Ying Huang,Minhua Su,Yuying Xie,Diyun Chen

Heterocyclic aromatic compounds such as malachite green can cause immense harm to the environment and mankind because of their toxic bio-accumulation and insufficient biodegradation. ZnFe 2 O 4 /TiO 2 (ZF-T) has attracted attentions as a visible-light-driven catalyst because it can break and mineralize benzene through photolysis. Compared with TiO 2 , which photodegrades only 53.5% malachite green, anatase TiO 2 loaded with ZnFe 2 O 4 has greater photocatalytic activity and can degrade up to 90.1% malachite green. Furthermore, a photocatalytic efficiency above 80% can be obtained through five consecutive cycles with a duration of 4 h. In this study, ZF-T was characterized, and its photolytic parameters, including dosage, pH, time, and ionic strength, were optimized. The photolytic products of malachite green were analyzed by ultraviolet–visible spectroscopy and liquid chromatography-mass spectrometry, which confirmed that ZF-T can drive visible light to produce •O 2 − and H + free radicals that can efficiently degrade heterocyclic aromatic hydrocarbons and cleave benzene rings. These outcomes deepen our understanding of the development and applications of visible-light-driven ZF-T composites in the field of wastewater purification.

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Journal of Asian Ceramic Societies · 2022 · IF 2.546

Digital light processing 3D printing of surface-oxidized Si3N4 coated by silane coupling agent

Ping Yang,Zhenfei Sun,Shengwu Huang,Jun Ou,Qiangguo Jiang,Dichen Li,Shanghua Wu

Due to high light absorption and high refractive index of silicon nitride (Si3N4) ceramic, it is difficult to prepare Si3N4 slurry with favorable curing ability, high solid loading and low viscosity at the same time, and thus the high-quality Si3N4 parts are hard to fabricate via Digital Light Processing (DLP). In this paper, the oxidation process was used to enhance the curing behavior of Si3N4 slurry, and then silane coupling agent (KH560) was used to improve the rheological properties of the oxidized Si3N4 slurry. The effect of Si3N4 slurry with oxidation and modification on its rheological behavior, light absorption, curing ability and stability have been systematically investigated. A Si3N4 slurry with abundant photocuring ability, high solid loading, low viscosity and reliable stability was fabricated by the oxidized (1 h) and KH560 (1 wt.%) modified Si3N4 powders, and the dense Si3N4 ceramic parts were produced by this slurry via DLP 3D printing. Subsequently, the influence of oxidation and modification on microstructure, mechanical properties and thermal conductivity have been investigated. Finally, the microstructure and performances of Si3N4 ceramic were compared between different forming processes (including: DLP and cool isostatic pressing).

CAS / MDL: 1309-48-4 25322-68-3
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

Hierarchical Ti3C2 MXene/Zn3In2S6 Schottky junction for efficient visible-light-driven Cr(VI) photoreduction

Hongfei Yin,Chunyu Yuan,Huijun Lv,Kaiyue Zhang,Xue Chen,Yongzheng Zhang

Environmental crisis aroused from the Cr(VI)-containing wastewater has received much attention, due to the cancer-causing and mutagenic feature of Cr(VI). Photocatalytic technology has been considered to be a favorable contestant for coping with Cr(VI)-containing effluent. In this study, Ti 3 C 2 MXene/Zn 3 In 2 S 6 Schottky junctions with different content of Ti 3 C 2 MXene were prepared for Cr(VI) photoreduction. The inherent physical and photoelectrochemical characters of the obtained Ti 3 C 2 MXene/Zn 3 In 2 S 6 Schottky junctions were fully characterized. Compared with the pure Zn 3 In 2 S 6 , all the nanocomposites showed enhanced photocatalytic performance, the apparent kinetic constant of the optimized sample was 3.17 times the height of the Zn 3 In 2 S 6 . The improved photoreduction performance largely originated from the effectual separation and transfer of the photoexcited charge carriers. In the meantime, the deleterious role of superoxide radicals for Cr(VI) photoreduction was confirmed. It is anticipated this research can deliver a new-fangled vision for constructing efficient photocatalyst for Cr(VI) photoreduction.

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Alexandria Engineering Journal · 2021 · IF 3.732

Developing a novel strategy for light-triggered reversible enzyme immobilization and reuse of support

Yaya Wang,Yuqi Gu,Shun Yang

The reuse of support material still hamper the practical application of enzyme immobilization technology in wastewater treatment. Here, a novel strategy based on light-triggered reversible β-cyclodextrin (β-CD)-Azobenzene(Azo) host-guest interaction was developed. First, magnetic Fe 3 O 4 nanoparticles were coated with porous β-CD-containing polymers(PCDP), and then the Azo-modified enzyme was immobilized in normal condition. The immobilization would enhance the stability and catalytic performance of enzymes, and the easy separation from reaction medium could be available with external magnetic field. Over broad ranges of temperature and pH, the immobilized enzyme showed higher activity than free enzyme, and the phenol removal efficiency retained about 58.63% even after five cycles. Under UV light, the photoisomerization of Azo would lead to disassemble of β-CD-Azo interaction, resulting in the detachment of the enzyme, and phenol removal efficiency decreased to only 16%. The support materials could be recovered for continue enzyme immobilization, results based on cyclic process of enzyme immobilization and detachment strongly demonstrated the detachment of enzyme and excellent reusability of Fe 3 O 4 @PCDP. And this strategy was proved to be a practical method based on batch experiments on the removal of phenol by tyrosinase (Tyr)-based remediation.

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APPLIED SURFACE SCIENCE · 2021 · IF 6.707

Constructing porous polyimide/carbon quantum dots aerogel with efficient photocatalytic property under visible light

Yujie Bai,Xibin Yi,Bing Li,Shiwei Chen,Zijie Fan

Polyimide was widely studied as semiconductor polymer photocatalyst. However, polyimide photocatalyst suffers from small specific surface area, poor visible light absorption and low charge thansfer efficiency. Herein, porous polyimide/carbon quantum dots aerogel was prepared successfully via supercritical CO 2 drying method. The carbon quantum dots were obtained by a green hydrothermal method. The carbon quantum dots could be anchored intimately on the polyimide aerogel by π -π stacking interactions. The polyimide/carbon quantum dots aerogel had large specific surface area and porous structure. The carbon quantum dots increased the visible light absorption, adjusted the band structure of the polyimide aerogel and facilitated the generation and separation of photogenerated electron and holes. Thus the photocatalytic property of the polyimide/carbon quantum dots aerogel was increased compared to pure polyimide aerogel. h + and ·O 2 – were the main active species to degrade the pollutant. Finally, the mechanism of the photocatalysis under the visible light was proposed.

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DALTON TRANSACTIONS · 2021 ·Vol. 50 ·期 45 ·16711-16719 · IF 4.39

Immobilizing CsPbBr3 perovskite nanocrystals on nanoporous carbon powder for visible-light-driven CO2 photoreduction

Ying Jiang,Cunxin Mei,Zhijie Zhang,Zhongliang Dong

Perovskite CsPbBr3 nanocrystals (NCs) have emerged as promising candidates for the photocatalytic reduction of CO2. However, the CO2 conversion efficiency of pristine CsPbBr3 is still unsatisfactory, mainly due to severe radiative recombination, poor stability and low CO2 capturing ability. Coincidentally, nanoporous carbon powder (NCP) has received tremendous attention for environmental remediation and renewable energy production. Herein, by immobilizing CsPbBr3 NCs into the pores of NCP, a CsPbBr3/NCP hybrid has been successfully constructed for the first time, which combined the advantages of CsPbBr3 NCs and NCP. In comparison with pristine CsPbBr3, the resultant hybrid photocatalyst exhibited much superior photocatalytic performance in CO2 reduction, which could be attributed to the enhanced electron extraction and transfer between CsPbBr3 NCs and NCP, higher CO2 capturing ability and more active sites for CO2 activation. Furthermore, the nanohybrid displayed remarkable reusability in photocatalytic CO2 reduction. This study is anticipated to provide a new pathway for the design and fabrication of high-performance photocatalysts based on perovskites for solar-energy-conversion applications.

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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 22 ·26465-26479 · IF 2.478

The fast degradation for tetracycline over the Ag/AgBr/BiOBr photocatalyst under visible light

Zhu Wanrong,Song Jimei,Wang Xule,Lu Yun,Hu Gang,Yang Jie

A series of Ag/AgBr/BiOBr photocatalysts with different weight contents of Ag/AgBr were successfully constructed via a simple precipitation method in 80 °C water bath. Photocatalysts were characterized by XRD, XPS, SEM, TEM, N 2 Adsorption-Desorption (BET), and UV–Vis Diffuse Reflectance Spectroscopy (DRS). Compared with BiOBr and Ag/AgBr, all the composite photocatalysts show the prominent photocatalytic activity for the degradation of tetracycline (TC). Especially, 1:5Ag/AgBr/BiOBr (20%) has the highest reaction rate constant (kapp = 0.20 min −1 ). Moreover, according to the results of radical scavengers runs, ·OH and h + acted as the main reactive species in the degradation process. Based on above, a possible photocatalytic mechanism for organics degradation over Ag/AgBr/BiOBr was proposed. Interestingly, the redox cycle between O 2 /·O 2 − and Br − /Br 0 assisted with the surface plasmon resonance (SPR) effect of silver dramatically promotes the separation and transfer of electron–hole pairs, and improves the photocatalytic activity of the as-obtained composite samples.

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Advanced Photonics Research · 2021 ·Vol. 2 ·期 12 ·2100143 · IF 0

Highly Efficient White-Light Emission Triggered by Sb3+ Dopant in Indium-Based Double Perovskites

Bo Zhou,Zexiang Liu,Henan Li,Shaofan Fang,Feier Fang,Ye Wang,Fuming Chen,Yumeng Shi

Inorganic indium-based halide double perovskites (DPs) are environmentally friendly alternatives to lead-based halide perovskites in light-emitting diodes, but commonly suffer from low quantum efficiency and harsh synthesis conditions. Herein, a large-scale green method using water as solvent is developed for the synthesis of 3D Cs 2 NaInCl 6 and 0D Cs 2 InCl 5 ·H 2 O with/without Sb 3+ dopant at room temperature. The transformation between Cs 2 InCl 5 ·H 2 O and Cs 2 NaInCl 6 products is controlled by the concentration of eco-friendly NaCl, where excess Cl − and Na + ions play important roles in inhibiting In 3+ hydrolysis and promoting Cs 2 NaInCl 6 crystallization, respectively. The obtained Cs 2 NaInCl 6 :Sb and Cs 2 InCl 5 ·H 2 O:Sb exhibit highly luminescent self-trapped exciton-related blue (450 nm; photoluminescence quantum yield [PLQY] ≈85%) and yellow (610 nm; PLQY ≈88%) emissions, which are comparable to those obtained by previous methods. Tunable cold/warm white light with a PLQY of up to ≈73% is achieved by the rational assembly of two components with highly overlapped excitation wavelength ranges. Each component demonstrates remarkable stability against humidity and heat. This composite shows great potential in solid-state lighting for general illumination.

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INORGANIC CHEMISTRY COMMUNICATIONS · 2021 · IF 2.495

Ethanol-assisted molten salt synthesis of Bi4Ti3O12/Bi2Ti2O7 with enhanced visible light photocatalytic performance

Yujing Ou,Junqing Shi,Quanqing Yan,Chunlei Li,Yi Zheng

Molten salt synthesis is an efficient method for preparation of photocatalyst. Enhancing precursor mixing effect is important. In this study, we found ethanol is important for synthsis of face-to-face type Bi 4 Ti 3 O 12 /Bi 2 Ti 2 O 7 composite photocatalyst. The prepared Bi 4 Ti 3 O 12 /Bi 2 Ti 2 O 7 (B3) composite under molar ratio of Bi:Ti of 4:3.6 displays higher photocatalytic activity compared with Bi 4 Ti 3 O 12 (B1) and Bi 2 Ti 2 O 7 (B4). The photocurrent density of B3 is 2 times higher than B1 and 1.6 times higher than B4, and B3 has smallest charge resistance between sample and solution. Combined with XPS, the study found that the higher photocatalytic activity origins from large charge transfer interface and built-in electric field (BIEF) around such interface, rathor than light absorption and dark adsorption.

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ADVANCED FUNCTIONAL MATERIALS · 2021 ·Vol. 31 ·期 47 ·2105383 · IF 18.808

Injectable Hydrogel with NIR Light-Responsive, Dual-Mode PTH Release for Osteoregeneration in Osteoporosis

Lijun Kuang,Jinghuan Huang,Yutong Liu,Xiaolin Li,Yuan Yuan,Changsheng Liu

Effective treatments to overcome osteoblast/osteoclast imbalance are the key to achieving desirable bone regeneration for osteoporosis patients. When used for local bone repair, parathyroid hormone (PTH) often leads to either excessive osteoclasts under continuous exposure or insufficient osteoclasts with pulsatile release of PTH. Herein, an injectable multifunctional in situ-generated calcium phosphate nanoparticle (ICPN)-coordinated poly(dimethylaminoethyl methacrylate-co-2-hydroxyethyl methacrylate) (DHCP) hydrogel loaded with PTH for near-infrared (NIR)-stimulated release is developed to achieve bone regeneration in an ovariectomized (OVX) model. Photothermal-responsive poly(N-acryloyl glycinamide-co-acrylamide) PNAm-indocyanine green ICG-PTH microspheres (PIP MSs) endow a dual-mode release system with a sustained release at low concentrations, a pulse release of PTH, and in situ pore formation properties. The PIP MS-encapsulated DHCP hydrogel (DHCP-10PIP/d) is injected into the bone defects of OVX rats. Under NIR irradiation, the localized photothermal effects trigger on-demand PTH release and in situ micropores formation through the gel–sol transition of PIP MSs, and the repeated treatment is harmless to the bioactivity of PTH. This platform can enhance osteoblast and osteoclast activity at the same time both in vitro and in vivo and repair the cranial defects of OVX rats successfully. Overall, this work provides a promising strategy for PTH delivery to repair osteoporotic bone defects.

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