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411.
Lina Sun Yi Cao Wenjing Li Li Wang Pi Ding Zhongzhong Lu Fanshu Ma Zheng Wang Renjun Pei 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(27):2300101
Sonodynamic therapy (SDT) has attracted intensive attention, but is still hindered by low sonosensitization and non-biodegradability of the traditional sonosensitizers. Herein, perovskite-type manganese vanadate (MnVO3) sonosensitizers integrating high reactive oxide species (ROS) production efficiency and appropriate bio-degradability are developed for enhanced SDT. Taking advantage of the intrinsic properties of perovskites such as narrow bandgap and substantial oxygen vacancies, MnVO3 shows a facile ultrasound (US)-triggered electrons-holes separation and restrained recombination, thus enhancing the ROS quantum yield in SDT. Furthermore, MnVO3 exhibits a considerable chemodynamic therapy (CDT) effect under the acidic condition probably owing to the presence of manganese and vanadium ions. Due to the presence of high-valent vanadium, MnVO3 can also eliminate glutathione (GSH) within the tumor microenvironment, which synergistically amplifies the efficacy of SDT and CDT. Importantly, the perovskite structure bestows MnVO3 with superior biodegradability, which alleviates the long-term presence of residues in metabolic organs after therapeutic actions. Based on these characteristics, US-assisted MnVO3 achieves an excellent antitumor outcome along with low systemic toxicity. Overall, perovskite-type MnVO3 may be promising sonosensitizers for highly efficient and safe treatment of cancer. The work attempts to explore the potential utility of perovskites in the design of degradable sonosensitizers. 相似文献
412.
Haotian Jiang Yinglai Hou Zengwei Liu Ruizhe Yuan Yu Du Xiaofei Ji Zhizhi Sheng Xuetong Zhang 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(41):2302627
The pursuit of efficient CO2 capture materials remains an unmet challenge. Especially, meeting both high sorption capacity and fast uptake kinetics is an ongoing effort in the development of CO2 sorbents. Here, a strategy to exploit liquid-in-aerogel porous composites (LIAPCs) that allow for highly effective CO2 capture and selective CO2/N2 separation, is reported. Interestingly, the functional liquid tetraethylenepentamine (TEPA) is partially filled into the air pockets of SiO2 aerogel with left permanent porosity. Notably, the confined liquid thickness is 10.9–19.5 nm, which can be vividly probed by the atomic force microscope and rationalized by tailoring the liquid composition and amount. LIAPCs achieve high affinity between the functional liquid and solid porous counterpart, good structure integrity, and robust thermal stability. LIAPCs exhibit superb CO2 uptake capacity (5.44 mmol g−1, 75 °C, and 15 vol% CO2), fast sorption kinetics, and high amine efficiency. Furthermore, LIAPCs ensure long-term adsorption–desorption cycle stability and offer exceptional CO2/N2 selectivity both in dry and humid conditions, with a separation factor up to 1182.68 at a humidity of 1%. This approach offers the prospect of efficient CO2 capture and gas separation, shedding light on new possibilities to make the next-generation sorption materials for CO2 utilization. 相似文献
413.
《NDT International》1989,22(4):245
414.
Xiaofei Ji Wusong Zha Qun Luo Guangyong Li Yu Du Xuetong Zhang 《Small (Weinheim an der Bergstrasse, Germany)》2023,19(34):2301534
The super-white body might be defined as its reflectivity exceeding 98% at any angle in the visible light spectrum, which can be used in a variety of emerging fields including optics, energy, environment, aerospace, etc. However, elaborate synthesis of a light-weight, highly reflective super-white aerogel body remains a great challenge. In this work, fine-tuning of silica aerogel co-hydrolyzed precursor ratios, 99.7% reflectivity with angle-independence in the visible light spectrum has been successfully achieved when the areal density is only 0.129 g cm−2, which breaks through the theoretical bandwidth limit of photonic crystals as well as the measured reflectivity limit of conventional porous materials. Furthermore, the reflectivity of super-white silica aerogel remains unchanged after various harsh deformations including compression and bending 1000 times, solar (≈800 W m−2), ultraviolet (≈0.68 W m−2), and humidity (100%) aging for 100 days, liquid nitrogen (−196 °C) and high-temperature (300 °C) thermal shock 100 times. As proofs of performance, the resulting super-white silica aerogels have been used as the novel standard white plate for better spectrum calibration, as the flexible projector curtains for optical display, as well as the transmitted light reflective layer in the photovoltaic cell for improving the relative power conversion efficiency of 5.6%. 相似文献
415.
Kangdi Niu Guotao Qiu Chuanshou Wang Daiyue Li Yutao Niu Songge Li Lixing Kang Yongqing Cai Mengjiao Han Junhao Lin 《Advanced functional materials》2023,33(2):2208528
Emerging 2D magnetic heterojunctions attract substantial interest due to their potential applications in spintronics. Achieving magnetic phase engineering with structural integrity in 2D heterojunctions is of paramount importance for their magnetism manipulation. Herein, starting with chromium ditelluride (CrTe2) as the backbone framework, various lateral and vertical magnetic heterojunctions are obtained via self-intercalated 2D chromium telluride (CrxTey). A Cr2Te3-Cr5Te8 lateral heterojunction prototype is demonstrated for the manipulation of magnetic moments under different magnitudes of magnetic excitation, showing a sharply stepped hysteresis loop with a dual spin-flip transition at high Curie temperatures up to 150 and 210 K by magneto-optical Kerr measurement. High-resolution scanning transmission electron microscopy and first-principles calculations reveal a preferred random location of Cr intercalants at the phase boundary, allowing lowering energy associated with crystal field splitting. The overall structural rigidity of chromium-telluride heterostructure with magnetic phase decoupled behaviors is promising for 2D spintronic devices. 相似文献
416.
Feng Zhang Lu Tan Li Gong Shuqi Liu Wangxi Fang Zhenggong Wang Shoujian Gao Jian Jin 《Frontiers of Chemical Science and Engineering》2022,16(5):699
Layer-by-layer assembly is a versatile technique for fabricating nanofiltration membranes, where multiple layers of polyelectrolytes are usually required to achieve reasonable separation performance. In this work, an ionic strength directed self-assembly procedure is described for the preparation of nanofiltration membranes consisting of only a single bilayer of poly(diallyldimethylammoniumchloride) and poly(sodium-4-styrenesulfoate). The influence of background ionic strength as well as membrane substrate properties on the formation of single-bilayer membranes are systematically evaluated. Such a simplified polyelectrolyte deposition procedure results in membranes having outstanding separation performance with permeating flux of 14.2 ± 1.5 L∙m–2∙h–1∙bar–1 and Na2SO4 rejection of 97.1% ± 0.8% under a low applied pressure of 1 bar. These results surpass the ones for conventional multilayered polyelectrolyte membranes. This work encompasses an investigation of ionic strength induced coiling of the polyelectrolyte chains and emphasizes the interplay between-polyelectrolyte chain configuration and substrate pore profile. It thus introduces a new concept on the control of membrane fabrication process toward high performance nanofiltration. 相似文献
417.
Lifeng Sang Xingze Chen Jin Fang Peng Xu Wenming Tian Ke Shui Yunfei Han Hao Wang Rong Huang Qing Zhang Qun Luo Chang-Qi Ma 《Advanced functional materials》2023,33(45):2304824
Inkjet printing (IJP) is a roll-to-roll (R2R) compatible fabrication method for large-area organic solar cells (OSCs). Unlike the coating process, the films are formed through droplet leveling and merging during IJP, and the pre-deposited droplets are partly dissolved by the subsequent droplets. Such a process yields undesired printing pattern lines, especially in large-area printed films. This study reveals that such a temperature-dependent “drying lines-related” phase separation morphology has caused component variation in the organic blend films, which leads to an obvious inhomogeneity of photocurrent in the printed OSCs. Such a phenomenon is attributed to the solubility difference between organic donor and acceptor molecules in the main printing solvent. A composite solvent strategy of ortho-dichlorobenzene (oDCB)/trimethylbenzene (TMB) and tetralin (THN) is developed to solve this problem. The introduction of THN suppresses the formation of printing drying lines during high-temperature printing due to the preferential miscibility of acceptor in THN, leading to the efficiency improvement to 13.96% and 15.78% for the binary and ternary devices. In addition, the 1 cm2 device with a disruptive pattern gives an efficiency of 12.80% and a certificated efficiency of 12.18%. 相似文献
418.
Ying Zhang Shuanghao Zheng Caixia Meng Hanqing Liu Cong Dong Xiaoyu Shi Pratteek Das Rong Huang Yan Yu Zhong-Shuai Wu 《Advanced functional materials》2023,33(30):2300987
Lithium-rich layered oxides (LROs) are one class of the most competitive high-capacity cathode materials due to their anion/cation synergistic redox activity. However, excessive oxidation of the oxygen sublattices can induce serious oxygen loss and structural imbalance. Hence, a near-surface reconfiguration strategy by fluorinating graphene is proposed to precisely regulate Mn3+/Mn4+ and O2−/(O2)n− redox couples for remarkably stabilizing high-capacity LROs and realizing the simultaneous reduction of the lattice stress, regulation of the Mn metal at a lower charge state, and construction of 3D Li+ diffusion channels. Combining with a highly conductive graphene-coating layer, the surface oxygen loss, transition metal dissolution, and electrolyte catalytic decomposition are suppressed. Benefiting from this synergy, the modified LROs disclose higher initial Coulombic efficiency and discharge-specific capacity and improve cyclability compared with pristine LROs. Further, it is revealed that the F− impact becomes easier for the O sites at the lattice interface of C2/m and Rm to sufficiently buffer lattice stress. Moreover, lithium ions coupled to the doped F atoms at the lattice interface migrate to the Ni-rich Rm lattice sites with lower migration energies. This consolidated understanding will open new avenues to regulate reversible oxygen redox of LROs for high-energy-density lithium-ion batteries. 相似文献
419.
Rui Pan Fuhan Cui Anqi Zheng Guoju Zhang Zhenjing Jiang Yuwei Xiong Lei Wei Qichong Zhang Litao Sun Kuibo Yin 《Advanced functional materials》2023,33(33):2300619
Flexible aqueous zinc-ion batteries (AZIBs) with high safety and low cost hold great promise for potential applications in wearable electronics, but the strong electrostatic interaction between Zn2+ and crystalline structures, and the traditional cathodes with single cationic redox center remain stumbling blocks to developing high-performance AZIBs. Herein, freestanding amorphous vanadium oxysulfide (AVSO) cathodes with abundant defects and auxiliary anionic redox centers are developed via in situ anodic oxidation strategy. The well-designed amorphous AVSO cathodes demonstrate numerous Zn2+ isotropic pathways and rapid reaction kinetics, performing a high reversible capacity of 538.7 mAhg-1 and high-rate capability (237.8 mAhg-1@40Ag-1). Experimental results and theoretical simulations reveal that vanadium cations serve as the main redox centers while sulfur anions in AVSO cathode as the supporting redox centers to compensate local electron-transfer ability of active sites. Significantly, the amorphous structure with sulfur chemistry can tolerate volumetric change upon Zn2+/H+ insertion and weaken electrostatic interaction between Zn2+ and host materials. Consequently, the AVSO composites display alleviated structural degradation and exceptional long-term cyclability (89.8% retention after 20 000 cycles at 40 Ag-1). This work can be generally extended to various freestanding amorphous cathode materials of multiple redox reactions, inspiring development of designing ultrafast and long-life wearable AZIBs. 相似文献
420.
Time temperature indicators (TTIs) based on a dye sublimation process have been developed for full time monitoring of heat sensitive vaccines with shorter shelf-life during cold chain transportation and storage. The structure of TTI and the methods to make the TTI are introduced. TTI 1 and TTI 2 introduced in the article were made with methyl azulene-1-carboxylate and methyl 3-methylazulene-1-carboxylate as the functional dyes, respectively. The kinetic parameters of TTI 1 and TTI 2 were studied. To achieve a change of 30 in ∆E*ab, it takes 9.1 h at 37°C, 39.7 h at 25°C, 5.61 days at 15°C and 23.3 days at 5°C for TTI 1 and 37.2 h at 37°C, 128.8 h at 25°C, 37.5 days at 15°C and 102.5 days at 5°C for TTI 2. The activation energies (Ea) are calculated to be 91.87 kJ mol−1 and 97.99 kJ mol−1 for TTI 1 and TTI 2, respectively. A field simulation study was conducted on TTI 2 associated with bivalent oral polio vaccine (bOPV), yielding excellent correlation between the reaction rate of TTI 2 and the titre change of bOPV. 相似文献