APPLIED CATALYSIS B-ENVIRONMENTAL
·
2017
·
IF 9.446
Jibo Liu,Huijie Shi,Qi Shen,Chenyan Guo,Guohua Zhao
Aiming at improving the efficiency of photoelectrocatalytic (PEC) CO 2 conversion to methanol, a heterogeneous photoelectrocatalyst was prepared by covalently binding a Ru(II) metal-organic complex (Ru-Py) containing exposed pyridyl on the periodic TiO 2 nanotube arrays (TNTAs). PEC characterization indicated that the Ru-Py/TNTAs photocathode exhibited excellent PEC CO 2 reduction activity in aqueous solution. The initial CO 2 reduction potential on Ru-Py/TNTAs photocathode reached −0.4 V (vs. NHE) under simulated solar irradiation. The cathodic photocurrent response of Ru-Py/TNTAs in CO 2 -satuarated aqueous solution was about 1.79 mAcm −2 , which was 2.4 times that of TNTAs . It may be caused by the enhanced light absorption in the visible region originated from Ru-Py. Meanwhile, Ru-Py played an important role in accelerating the separation of photoinduced electron-hole pairs evidenced by the photoluminescence spectra. PEC CO 2 reduction test showed that 84.8 μmol methanol was produced with 63.9% faraday efficiency, 62.6 turnover number (TON) and 45% selectivity at −0.9 V under 8 h irradiation. Furthermore, the non-covalent bonded system only produced 41.3 μmol methanol indicating that the carboxylic covalent linking displayed excellent electron transfer efficiency and methanolization performance. The mechanism investigation revealed that the exposed pyridyl provided the active sites in forming pyridiniumformate intermediates confirmed by the differential UV–vis absorption ( ΔA ) spectrum, which was of great significance in the efficient CO 2 methanolization. The probable reaction pathway for catalytic CO 2 reduction to methanol was also proposed combining the possible intermediates detected by gas chromatography mass spectrometry (GCMS).
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JOURNAL OF HAZARDOUS MATERIALS
·
2025
·
IF 11.3
Xinru Li,Jiale Li,Zhichao Liu,Can Liu,Yafei Guo,Tianlong Deng
The effective removal of strontium (Sr) from radioactive wastewater is essential for human health and ecological sustainability. However, due to the existence of a large number of coexisting ions, the selective removal of Sr 2+ from it remains a significant challenge. Herein, three novel metal-doped sodium vanadosilicates were developed by structural regulation. It was found that Co-doping can not only significantly reduce the dissolution loss of vanadosilicate (NaVOSi) from the adsorbent in extreme environments by adjusting the orbital energy distribution, energy band structure, bond length, and bond energy of sodium vanadosilicate crystals, but also further enhance the adsorption performance by reducing its zeta potentials and agglomeration phenomenon. The maximum adsorption capacity of the developed adsorbent (Co-NaVOSi) was up to 319.10 mg·g −1 within 5 min. When applied to Sr 2+ removal from simulated wastewater, the distribution coefficients of Sr 2+ reached 2943.15 mL·g −1 , and the separation coefficients between Sr 2+ and coexisting ions were above 64. DFT calculations further revealed the highly selective removal mechanism of Sr 2+ from wastewater. In addition, NaNO 3 was proved to be an efficient eluent. The excellent properties above make NaVOSi an excellent candidate for effectively removing Sr 2+ from wastewater.
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MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING
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2025
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IF 7
Yu He,Shengwei Xin,Baoru Sun,Xuecheng Cai,Yapeng Lin,Lingwei Kong,Xun Shen,Congcong Du,Xiaoyuan Yuan,Kangkang Wen,Tongde Shen
Metals are often soft while ceramics are often hard. To make metals as hard as ceramics has been long-awaited in metals and ceramics communities. In this study, bulk nanocrystalline (NC) tungsten-1 wt% yttrium-0.7 wt% titanium (WYT) was fabricated via mechanical alloying followed by high-temperature/high-pressure sintering. The high pressure directly inhibits grain growth by suppressing atomic diffusion and indirectly inhibits grain growth by lowering sintering temperature, enabling the synthesis of dense NC WYT bulks with an average grain size of ∼ 9.0 nm. The high temperature causes annealing- and segregation-induced structural relaxation of grain boundaries (GBs) in sintered bulk NC WYT, resulting in GBs with a small excess volume of only ∼ 0.005 nm, one fifth that of bulk NC tungsten. The small grain size and the relaxed GBs in the bulk NC WYT make it hard for GBs to emit dislocations, resulting in extremely high hardness of 23.2 ± 0.3 GPa, yield strength of 9.4 ± 0.3 GPa, and ultimate compressive strength of 13.1 ± 1.1 GPa. The hardness of metallic bulk NC WYT is comparable to that of ceramic tungsten carbide (WC) whereas the wear rate of bulk NC WYT is even lower than that of WC. The structure-relaxed GBs lower the thermodynamic driving force for grain growth and result in an extremely high thermal stability - no grain growth occurs in bulk NC WYT annealed at a high temperature of 1500 °C, which is above the recrystallization temperature of tungsten. The present strategy - multifunctional treatments of NC alloy powders by high-temperature/high-pressure - provides a huge potential to manufacture dense bulk NC materials with exceptional mechanical property and thermal stability for practical applications.
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Inorganics
·
2025
·Vol. 13
·期 3
·74
·
IF 3
Yan Chu,Shiwei Fang,Yingjue Chen,Xiaoqi Zhang,Jie Zheng,Zhenglong Li,Wubin Du,Wengang Cui,Jian Miao,Yaxiong Yang,Yongfeng Liu,Mingxia Gao,Hongge Pan
LiAlH4, characterized by high hydrogen capacity and metastable properties, is regarded as a promising hydrogen source under mild conditions. However, its reversible regeneration from dehydrogenated production is hindered thermodynamically and kinetically. Herein, we demonstrate an active Li–Al–Ti nanocrystalline alloy prepared by melt spinning and cryomilling to enable directly synthesizing nano-LiAlH4. Due to the non-equilibrium preparation methods, the grain/particle size of the alloy was reduced, stress defects were introduced, and the dispersion of the Ti catalyst was promoted. The refined Li–Al–Ti nanocrystalline alloy with abundant defects and uniform catalytic sites demonstrated a high reactivity of the particle surface, thereby enhancing hydrogen absorption and desorption kinetics. Nano-LiAlH4was directly obtained by ball milling a 5% Ti containing Li–Al–Ti nanocrystalline alloy with a grain size of 17.4 nm and Al3Ti catalytic phase distributed under 20 bar hydrogen pressure for 16 h. The obtained LiAlH4exhibited room temperature dehydrogenation performance and good reversibility. This finding provides a potential strategy for the non-solvent synthesis and direct hydrogenation of metastable LiAlH4hydrogen storage materials.
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RSC Advances
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2025
·Vol. 15
·期 7
·5042-5059
·
IF 4.6
Irfan Ijaz,Aysha Bukhari,Ammara Nazir,Ezaz Gilani,Hina Zain,Attia Shaheen,Mohammed Rafi Shaik,Mujeeb Khan,Jilani P. Shaik
The simultaneous removal of antibiotics and heavy metal ions is of utmost importance because of their hazardous effects on the environment and humans. For the adsorption of sulfamethoxazole (SMX) and neodymium (Nd3+) in mono- and binary contaminant systems (SMX–Nd3+ and Nd3+–SMX), a novel composite was designed using sulfated fucan (FuS), MXenes, and α-aminophosphonates (AMPs) in this study. As far as we know, the concurrent adsorption of SMX and Nd3+ employing materials made of MXenes, FuS, and AMPs with this specific structure has not yet been reported. At 318 K, the FuS@MXene@AMP adsorbent demonstrated excellent adsorption capacities of 448.91 and 255.78 mg g−1 for SMX and Nd3+, respectively. The pseudo-first-order (PSO) kinetic model was the most appropriate for depicting the adsorption of SMX and Nd3+ among all the tested kinetic models. The adsorption of SMX and Nd3+ is better described by the Langmuir isotherm model with a higher value of adsorption capacity and R2. The simultaneous presence of Nd3+ and SMX promoted mutual sorption between the antibiotic and metal ions in the binary systems. The results of FTIR and XPS studies indicated that the removal mechanisms were primarily due to hydrogen bonding, complexation, electrostatic interaction, and π–π interaction.
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CHEMICAL ENGINEERING JOURNAL
·
2025
·
IF 13.2
Jiahao Yang,Zhaoping Shi,Yibo Wang,Hongxiang Wu,Jing Ni,Pengbo Wang,Meiling Xiao,Changpeng Liu,Wei Xing
Despite proton exchange membrane water electrolysis (PEMWE) being a commercially viable method for high-purity hydrogen production, the development of active and robust anode electrocatalysts with reduced iridium loading under high current density conditions remains highly challenging. Here, we report a core-shell nanostructured catalyst with a metallic titanium core uniformly covered by Ir nanoparticles (Ti@Ir). The spontaneously formed TiO x layer can effectively disperse Ir nanoparticles via interfacial Ti-O-Ir bonds, which in turn increases the oxidation state of Ir towards activated lattice oxygen reactivity, as confirmed by in-situ differential electrochemical mass spectrometry (DEMS). As a result, the Ti@Ir exhibits an overpotential of only 272 mV to reach 10 mA cm −2 , 17 mV lower than non-supported Ir nanoparticles, and a 3.82-fold higher mass activity at 1.53 V. Moreover, the Ti@Ir catalyst demonstrates strong stability during a 100-hour test at 10 mA cm −2 . Detailed analysis reveals that the oxidation of iridium close to the titanium core is suppressed. The huge potential for practical application is further confirmed in a PEMWE prototype, with a low iridium loading of 0.5 mg Ir cm −2 , significantly lower than the typical 2 ∼ 4 mg Ir cm −2 required for traditional catalysts. This Ti@Ir catalyst achieves a cell voltage of 1.858 V at an industrial-level current density of 2 A cm −2 and maintains stable operation for 1800 h with an exceptionally low voltage degradation rate of only 1.252 μV h −1 .
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Nature Communications
·
2025
·Vol. 16
·期 1
·1-13
·
IF 15.7
Liu Shaojia,Deng Jingjing,Zhao Hewei,Wang Tianbai,Lu Junfeng,Ding Baosen,Guo Tianqi,Ritchie Robert O.,Guo Lin
Stiffness-damping balance, high specific mechanical performance, and corrosion resistance are demanded for metals. Here, we developed an enamel-inspired ceramic (EIC) coating strategy involving hydrothermal growth of a tooth enamel-like ZrO₂ nanorods on Zr foil and amorphous ZrO₂ intergranular phase formation via controlled hydrolysis. The EIC coated Zr foil (Zr-EIC) achieved a high viscoelastic figure of merit (4.6 GPa); as well as excellent specific stiffness and hardness owing to the lightweight of ceramics, surpassing the values of Zr and previously reported Zr-based alloys or Zr-based composites. This was due to the vertically oriented stiff nanorods and unique energy dissipation derived from deformation at the crystalline/amorphous interfaces. It demonstrated exceptional NaCl corrosion resistance. This approach showed universality across Ti, Zn, and Cu substrates, enhancing both mechanical properties and corrosion resistance. By constructing an enamel-like hierarchical structure on the metal surface, the strategy overcomes traditional metal limitations without causing an increase in density.
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POLYMERS FOR ADVANCED TECHNOLOGIES
·
2025
·Vol. 36
·期 2
·e70128
·
IF 3.4
Yang Zhang,Qingsong Li,Xi Xie,Guoxin Sui
Most polymers and composites suffer from high friction and wear due to their inherent lack of self-lubrication under dry sliding friction. Herein, the lamellar Ti 3 SiC 2 MAX material is prepared via vacuum sintering of a powder mixture containing Ti, Si, and TiC in the molar ratio of 1:1.1:1.8 at 1500°C under a pressure of 30 MPa for 2 h. Combined with a soft graphite phase (5 wt%), self-lubricating PEEK/Graphite/Ti 3 SiC 2 (PG-T) composites are successfully prepared, dependent on Ti 3 SiC 2 (5 and 15 wt%) as a hard reinforced phase and lubrication additive. PG-T composites are fabricated via a multistep compounding approach using a twin-screw extruder. The incorporation of Ti 3 SiC 2 and graphite within the PEEK matrix manifests a highly pronounced synergistic effect, which not only facilitates effective lubrication but also significantly enhances the load-bearing capability, thereby effectively circumventing direct contact between the counterface and the polymeric matrix. The sliding tests are conducted on the pins (diameter: 6.0 mm, height: 17.0 mm) and friction pair (45#steel, roughness Ra: 148 nm) under dry friction. In terms of PV-condition (up to 6 MPa and 3 m/s) (PV is a parameter that reflects the load-bearing capacity of polymer materials, which is defined by multi-plying the pressure P by the sliding speed V), PG5-T15 exhibits self-lubricating properties, featured by an average coefficient of friction (ACOF) as low as 0.119 for the pin-plate test and a specific wear rate (SWR) of only 0.58 × 10 −6 mm 3 /Nm. Meanwhile, PG-T composites present excellent thermal properties based on the thermal expansion coefficients (CTEs) and storage moduli (G′) during friction and wear. Considering the practical applications of tribo-composites, these findings highlight the potential of PG-T composite as a candidate for demanding tribological applications.
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Materials Today Bio
·
2025
·
IF 10.2
Rui Chen,Zhiqi Yang,Yining Chen,Jinjie Wang,Yuhang Wang,Liqi Wei,Pengcheng Yu,Mengyuan Zhang,Yan Yan,Shuo Yang,Lili Wang,Yan Cheng
Hypoxia and electron-hole recombination are two obstacles limiting sonodynamic therapeutic efficacy against cancer. Herein, bismuth sulfide (Bi 2 S 3 )-titania (TiO 2 ) heterostructure is designed based on the excellent photothermal property of Bi 2 S 3 , which could improve intratumor oxygen content through increasing blood flow with the help of near infrared light. Bi 2 S 3 -TiO 2 heterostructure nanoparticles (NPs) present similar photothermal performance to Bi 2 S 3 NPs, while Bi 2 S 3 -TiO 2 NPs show higher reactive oxygen species (ROS) generating ability than Bi 2 S 3 NPs under ultrasonic irradiation. In vitro assessments proved that Bi 2 S 3 -TiO 2 NPs could produce heat and ROS to damage mitochondrial, leading to cell death due to their synergetic photothermal and sonodynamic performances. After being administrated into tumor, Bi 2 S 3 -TiO 2 NPs can effectively improve oxygen content at 8 h post 808 nm laser irradiation. The tumor growth inhibition rate of Bi 2 S 3 -TiO 2 NPs with 808 nm laser or ultrasound irradiation is 77.49 ± 3.96 % and 63.64 ± 2.2.7 %, respectively, while it reaches up 88.82 ± 3.98 % when 808 nm laser and ultrasound are applied in sequence, proving the photothermal amplified sonodynamic therapeutic efficacy against hypoxic tumor. As a result, the design of Bi 2 S 3 -TiO 2 heterostructure NPs realizes photothermal amplified sonodynamic therapy, providing a potential strategy for treating hypoxic tumors.
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LANGMUIR
·
2025
·
IF 3.9
Xi Zhang,Xixun Shen,Qian Chen,Jianping Tao,Wang Tang,Qunjie Xu
Surface icing poses a great challenge to the safe operation and energy output of wind turbines in low-temperature freezing rain environments. To address the problem of ice cover, we designed a durable superhydrophobic MWCNTs@[F-SiO2/TiN] composite anti-icing coating with a double-layer structure, where carbon nanotubes serve as the bottom layer and titanium nitride and fluorinated silica particles serve as the top layer. The introduction of TiN nanoparticles enhances the solidification rheological uniformity of the dispersion system of silica, resulting in the formation of a dense surface with a uniform micro/nanostructure. Such a micro/nanostructure not only endows the coating with excellent superhydrophobicity, with a large contact angle of about 171° and a small rolling angle of less than 1°, but also significant anti-icing performance. The freezing time of the water droplet on this composite coating was significantly delayed to 730 s at −20 °C in the static anti-icing experiment, which is about twice that of the pure silica coating. The simulated dynamic freezing rain experiments also show that this superhydrophobic coating can effectively prevent ice formation on the surfaces of fan blades. This composite coating also exhibits excellent electrical and photothermal effects, derived from its special double-layer structure and the ability of the titanium nitride external filler to reduce heat dissipation. Under the combined action of photothermal and electrothermal effects, this composite coating demonstrates excellent deicing ability, achieving rapid deicing within 206 s, about 25.2% improvement in deicing efficiency compared to coatings without TiN. In addition, this composite coating also exhibits superior structural and performance stability, even after thermal cycling, sand and water impact, and prolonged immersion in acid/alkali corrosion. The current results suggest that the designed superhydrophobic coating with a double-layer structure is a very promising candidate for practical anti-icing and deicing applications.
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INTERMETALLICS
·
2025
·
IF 4.8
Liangcai Du,Xiaoqing Liu,Qianqian Kong,Lichao Gong,Zhenhua Yao
Understanding the intricate phase transformations and their impact on the mechanical properties holds paramount importance in developing high entropy alloys (HEAs) with ideal properties, yet it remains challenging and underexplored. In this study, a series of novel CrFeMnNi (2-x) Ti x (x = 0, 0.5, 1, and 1.5 at.%) HEAs were meticulously designed based on the established Valence Electron Concentration (VEC) rule, with the VEC values systematically varied as the atomic composition (Ni, Ti) changed. The microstructure, phase transformation behavior, mechanical properties, and strengthening mechanisms were systematically investigated. We found that the HEA powders exhibited phase behavior consistent with the VEC rules. The spark plasma sintered (SPSed) HEA bulk samples exhibited a phase transformation attributed to the precipitation of Cr and Mn within the matrix, resulting in the formation of the σ phase. Quantitative calculation of the strengthening mechanisms revealed that grain boundary strengthening and precipitation strengthening were the primary contributors to the high strength of the HEA bulk samples. These findings not only advance the utilization of the VEC rules in HEA material design but also contribute to the understanding of the phase behavior and mechanical properties of HEAs, facilitating the design of high performance HEAs.
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EUROPEAN POLYMER JOURNAL
·
2025
·
IF 6.3
Yifei Ding,Wenxun Sun,Hongwei Gao,Ruiyu Zhang,Xiaobin Yang,Yongping Bai,Shuai Sun
High-transmittance polyester films are critical for advanced display technologies, yet the relationship between catalyst design and optical performance remains poorly understood. This work investigates seven metal-based catalysts and develops an economical and efficient composite catalyst accordingly. The highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energies of these catalysts are calculated using density functional theory (DFT) method. Results demonstrate that catalysts with lower LUMO energy levels can significantly promote nucleophilic attack during polycondensation, consequently exhibiting superior catalytic efficiency. Subsequently, we prepare a composite catalyst composed of cobalt(II) acetate tetrahydrate and germanium(IV) oxide. By employing the composite catalyst, the synthesized PET films achieved promising transmittance of 91.43 % and luminosity of 92.82 %. This study provides a DFT-driven strategy for designing optical polyesters, offering a scalable approach for advanced display applications.
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