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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Novel UiO-66/p-BN photocatalytic composites for efficient degradation of tetracycline under visible light

Xinyu Zhi,Jingjing Wang,Huayi Cai,Danyi Yang,Jinbo Jia,Tianliang Wang,Chengchun Tang,Yi Fang

Photocatalysis can directly convert solar energy into chemical energy, has shown unique advantages in solving environmental and energy problems. In this paper, novel UiO-66/p-BN (UBN) heterojunction photocatalysts were successfully prepared by a simple solvothermal method. UBN-6 achieved a degradation efficiency of up to 93.8 % for 30 mg/L tetracycline under 180 min of visible light irradiation, which was 2.46 and 3.25 times higher than that of pure UiO-66 and p-BN, respectively. The enhancement of UBN photocatalytic activity stemmed from the incorporation of p-BN, which increased the specific surface area to expose more active sites, broadened the visible light absorption range, and promoted the separation of photogenerated carriers through the formation of heterojunctions. Free radical trapping experiments showed that ·O 2 - , ·OH and h + played important roles in the photocatalytic degradation of tetracycline pollutants. In addition, the photocatalytic mechanism of UBN was revealed by analyzing the degradation intermediates of TC by LC-MS. This work provides an effective strategy for designing visible light responsive photocatalysts to degrade pollutants.

CAS / MDL: 10043-35-3 108-78-1
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LANGMUIR · 2025 · IF 3.9

Electroforming of Ni–P–PTFE Nanocomposites with Nanoscale Surface Roughness and Superior Self-Lubricating Properties

Zhigao Ma,Ziwen Wei,Bingyan Jiang,Lu Zhang

The electrodeposition of Ni–P–PTFE nanocomposites offers an effective approach to reduce mold–polymer interface adhesion and improve the replication of polymer micro features in injection molding. However, it is still challenging to fabricate Ni–P–PTFE nanocomposites with low internal stress and nanoscale surface roughness in electrolytes containing high PTFE concentrations. In this study, cetyltrimethylammonium bromide was introduced into the electrolytes to achieve a good dispersion of PTFE nanoparticles. Ni–P–PTFE nanocomposites with various compositions were successfully electrodeposited, and their tribological properties were analyzed. The electroformed Ni–P–PTFE nanocomposites with high PTFE and phosphorus contents showed a low surface roughness and surface energy compared to nickel electrodeposits. Ni–P–PTFE nanocomposites also exhibited a low coefficient of friction (COF) and wear loss when electroformed from an electrolyte containing 32 g/L phosphorus acid and 5 g/L PTFE nanoparticle. The COF of Ni–P–PTFE against stainless steel and poly(methyl methacrylate) was 0.2 and 0.12, respectively, representing a decrease of 80% and 85% compared to nickel electrodeposits. These enhancements in self-lubricating performances were primarily attributed to the low surface roughness and a shift in wear modes from adhesive wear to predominantly mild abrasive wear.

CAS / MDL: 128-44-9 57-09-0
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APPLIED SURFACE SCIENCE · 2025 · IF 6.9

P non-metal doping induced surface charge redistribution of VS2 for strengthening hydrogen evolution activity

Jingwei Wang,Yaoyong Dong,Xuejun Zheng,Bei long,Hui Ling,Long Xie,Zhenhua Xiang,Wenyuan He

This report reveals that the hydrogen evolution activity of VS 2 can be effectively strengthened by inducing the surface charge redistribution of VS 2 via P non-metal doping. The XRD, TEM, GPA, EDS and XPS characterizations confirm that the P atoms are successfully doped into the VS 2 /CC matrix by substituting S atoms, resulting in lattice tensile strain and charge redistribution. The optimal P-doped VS 2 on carbon cloth (P-VS 2 /CC) exhibits a low overpotential of 274 mV at − 50 mA cm −2 and a small Tafel slope of 65.4 mV dec -1 , much lower than those of VS 2 /CC counterpart (622 mV and 120.1 mV dec −1 , respectively). Moreover, the P-VS 2 /CC delivers a long-term stability for 55 h without decay at 10 mA cm −2 , outperforming the VS 2 /CC. Density functional theory calculations suggest that P doping can induce the charge transfer from S and V to nearby P atoms, resulting in the decrease of hydrogen adsorption free energy at the S and V sites and the increase of total density of states at the Fermi level, thus far super hydrogen evolution activity. This work provides a hopeful new route for strengthening the HER activity of VS 2 , and offers a new perspective for developing advanced transition-metal chalcogenides electrocatalysts.

CAS / MDL: 598-52-7 7803-55-6
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JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

β-Ga2O3 photodetectors with high-performance enhanced by field control via p-type NiO interlayer

Zeyulin Zhang,Dinghe Liu,Yiru Yan,Liru Zeng,Hao Chen,Qingwen Song,Dazheng Chen,Chunxiang Zhu,Chunfu Zhang,Yuming Zhang,Yue Hao

Gallium oxide (Ga 2 O 3 ) film exhibiting the solar-blind absorption cutoff characteristic holds considerable potential for application in UV photodetectors . The material defects in the device will introduce the recombination region for the photodetector, especially at the interface of the Ga₂O₃ heterojunction . The photogenerated carriers , generated within the Ga 2 O 3 film, will inevitably be influenced by these high recombination centers during their transportation. Avoiding or minimizing this region can improve the performance of the photodetector. The p-n junction, with its depletion region , generates an electric field that drives the carriers away from the recombination region. However, due to the Ga 2 O 3 p-type doping difficulty, our work focuses on the growth of single-crystal NiO/β-Ga₂O₃ films by Mist-CVD and the fabrication of field-controlled photodetectors. The hole concentration in the NiO film is adjusted by doping with different concentrations of Li⁺. Compared with a photodetector without the NiO interlayer, the performance of the photodetector with the structure of NiO (1 % Li⁺-doped)/β-Ga₂O₃ exhibits a significant improvement, which achieved the maximum responsivity of 1002.5 A/W, and a high peak detectivity of 3.31 × 10 15 Jones.

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LWT-FOOD SCIENCE AND TECHNOLOGY · 2025 · IF 6.6

Novel insights into p-cresol production in fermented bamboo shoots: Core microbiota and metabolic signatures

Xinyu Wang,Peilin Yu,Tao Wang,Chuanqi Chu,Zhijia Liu,Ming Du,Junjie Yi

p -Cresol has been identified as a key odorant that is responsible for the characteristic flavor of fermented bamboo shoots. Although it is known to play a significant role in bamboo shoot fermentation, the microbial sources and biosynthetic pathways of p -cresol is still poorly characterized. The relationship between the microbiota and flavor profiles in fermented bamboo shoots was systematically investigated in this study via metagenomics and gas chromatography–mass spectrometry (GC–MS). The results demonstrated that Lactobacillus and Kazachstania represented the dominant microbial genera, with Lactobacillus acetotolerans identified as the most abundant bacterial species. Phenols and acids were identified as the primary flavor components, and p -cresol was found to be the dominant flavor compound. Correlation analysis was further found to reveal significant positive associations between specific microorganisms (e.g., L. acetotolerans ) and key flavor compounds (including p- cresol). The formation of the main characteristic flavors in fermented bamboo shoots was closely associated with carbohydrate and amino acid metabolism pathways. Tyrosine was first converted to 4-hydroxyphenylacetate via transamination, followed by subsequent decarboxylation to p -cresol catalyzed by the enzyme 4-hydroxyphenylacetate decarboxylase. This study provides insights into the microbial mechanisms underlying the formation of the stinky flavor in fermented bamboo shoots.

CAS / MDL: 7452-79-1
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Biomaterials Science · 2022 ·Vol. 10 ·期 16 ·4576-4587 · IF 7.59

The osteogenic response to chirality-patterned surface potential distribution of CFO/P(VDF-TrFE) membranes

Jiamin Zhang,Xuzhao He,Zhiyuan Zhou,Xiaoyi Chen,Jiaqi Shao,Donghua Huang,Lingqing Dong,Jun Lin,Huiming Wang,Wenjian Weng,Kui Cheng

Piezoelectric poly(vinylidene fluoride-trifluoroethylene) has demonstrated an ability to promote osteogenesis, and biomaterials with a chirality-patterned topological surface could enhance cellular osteogenic differentiation. In this work, we created a chirality-patterned surface potential distribution of CoFe2O4/poly(vinylidene fluoride-trifluoroethylene (CFO/P(VDF-TrFE)) membranes to explore their osteogenic response under no change in surface chemical and topology, attempting to further strengthen the ability of the membranes to promote osteogenesis. The chirality-patterned surface potential distribution was established by microdomain contact polarization with the help of sinistral/dextral-patterned ITO interdigital microelectrodes. In the in vitro evaluations, the mesenchymal stem cells showed a positive response in osteogenic differentiation to CFO/P(VDF-TrFE) membranes with both sinistral- and dextral-patterned surface potential distributions, however, the dextral-patterned distribution gave a stronger response than the sinistral-patterned one. And the in vivo evaluation showed a response tend in new bone tissue formation similar to the in vitro evaluations. The stronger response in osteogenic differentiation and osteogenesis for the CFO/P(VDF-TrFE) membrane with the dextral-patterned distributions may be attributed to that the intense interaction of the cells with the electrophysiological microenvironment appears due to a correspondingly higher expression of integrin α5β1, which significantly up-regulates the Arp2/3 complex expression, a crucial factor for cytoskeleton reorganization, possibly increases cytoskeleton contractility, and strengthens the transduction of the osteogenesis-related signaling cascade. This work proves that the chirality-patterns in surface potential distributions could provide an osteogenic response similar to a chirality-patterned topological surface.

✓ 已验证 DOI PubMed 高影响因子
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Biomolecules · 2022 ·Vol. 12 ·期 7 ·997 · IF 6.064

Programmable Polyproteams of Tyrosine Ammonia Lyases as Cross-Linked Enzymes for Synthesizing p-Coumaric Acid

Mingyu Jia,Zhiyuan Luo,Haomin Chen,Bianqin Ma,Li Qiao,Qinjie Xiao,Pengfei Zhang,Anming Wang

Ideal immobilization with enhanced biocatalyst activity and thermostability enables natural enzymes to serve as a powerful tool to yield synthetically useful chemicals in industry. Such an enzymatic method strategy becomes easier and more convenient with the use of genetic and protein engineering. Here, we developed a covalent programmable polyproteam of tyrosine ammonia lyases (TAL-CLEs) by fusing SpyTag and SpyCatcher peptides into theN-terminal andC-terminal of the TAL, respectively. The resulting circular enzymes were clear after the spontaneous isopeptide bonds formed between the SpyTag and SpyCatcher. Furthermore, the catalytic performance of theTAL-CLEswas measured via a synthesis sample ofp-Coumaric acid. OurTAL-CLEsshowed excellent catalytic efficiency, with 98.31 ± 1.14% yield of the target product—which is 4.15 ± 0.08 times higher than that of traditional glutaraldehyde-mediated enzyme aggregates. They also showed over four times as much enzyme-activity as wild-type TAL does and demonstrated good reusability, and so may become a good candidate for industrial enzymes.Keywords:SpyTag/SpyCatcher;carrier-free immobilized enzyme;crosslinked enzyme protein;cell lysate;tyrosine ammonia lyase;bio-orthogonal system

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BIOMATERIALS · 2022 · IF 15.304

Programmed prodrug breaking the feedback regulation of P-selectin in plaque inflammation for atherosclerotic therapy

Quan Wang,Hongshu Jing,Jun Lin,Zhihua Wu,Yu Tian,Ke Gong,Qianqian Guo,Xupeng Yang,Liting Wang,Zhaojun Li,Yourong Duan

Inflammation is the main driver of the aggravation of arteriosclerosis, and the complex inflammatory response in plaque is usually the result of the interaction of various cells and cytokines. Therefore, it is difficult to comprehensively regulate the inflammatory process of arteriosclerosis by intervening a single target, resulting in the poor effect of existing treatment method. Based on our clinical findings that P-selectin stably and highly expressed in patients’ plaque endothelial cells, the programmed prodrug, low molecular weight heparin-indomethacin nanoparticles (LI NPs), were established as anti-inflammatory agent to multiphase inhibit arteriosclerosis by cascade interference of P-selectin. Structurally, LI NPs was obtained by simple esterification of low molecular weight heparin and indomethacin without any additives, guaranteeing the biocompatibility and applicability of LI NPs. Functionally, LI NPs could interfere with P-selectin in the inflammatory process, such as inhibiting macrophage adhesion, reducing the secretion of inflammatory factors, and inducing macrophage apoptosis. In the arteriosclerosis mice model, LI NPs significantly reduced the plaque area and showed satisfactory curative effect, which is related to the intervention of the multiphase inflammation between endothelial cells and macrophages. In conclusion, the programmed prodrug LI NPs offered a promising approach for the clinical therapy of arteriosclerosis.

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APPLIED MICROBIOLOGY AND BIOTECHNOLOGY · 2015 ·Vol. 99 ·期 10 ·4485-4494 · IF 3.337

The relief of microtherm inhibition for p-fluoronitrobenzene mineralization using electrical stimulation at low temperatures

Zhang Xueqin,Feng Huajun,Liang Yuxiang,Zhao Zhiqing,Long Yuyang,Fang Yuan,Wang Meizhen,Yin Jun,Shen Dongsheng

Low temperature aggravates biological treatment of refractory p -fluoronitrobenzene ( p -FNB) because of microtherm inhibition of microbial activity. Considering the potential characterization of energy supply for microbial metabolism and spurring microbial activity by electrical stimulation, a bioelectrochemical system (BES) was established to provide sustaining electrical stimulation for p -FNB mineralization at a low temperature. Electrical stimulation facilitated p -FNB treatment and bioelectrochemical reaction rate constants for the removal and defluorination of p -FNB at 10 °C were 0.0931 and 0.0054 h −1 , which were higher than the sums of the rates found using a biological system and an electrocatalytic system by 62.8 and 64.8 %, respectively. At a low temperature, microbial activity in terms of dehydrogenase and ATPase was found to be higher with electrical stimulation, being 121.1 and 100.1 % more active than that in the biological system. Moreover, stronger antioxidant ability was observed in the BES, which implied a better cold-resistance and relief of microtherm inhibition by electrical stimulation. Bacterial diversity analysis revealed a significant evolution of microbial community by electrical stimulation, and Clostridia was uniquely enriched. One bacterial sequence close to Pseudomonas became uniquely predominant, which appeared to be crucial for excellent p -FNB treatment performance in the BES at a low temperature. Economic evaluation revealed that the energy required to mineralize an extra mole of p -FNB was found to be 247 times higher by heating the system than by application of electrical stimulation. These results indicated that application of electrical stimulation is extremely promising for treating refractory waste at low temperatures.

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RSC Advances · 2021 ·Vol. 11 ·期 44 ·27207-27214 · IF 3.361

Design, synthesis, and herbicidal activity of sec-p-menthane-7-amine derivatives as botanical herbicides

Hongmei Zhang,Yuxiang Chen,Shichao Xu,Jing Wang,Huanhuan Dong,Zhendong Zhao,Jianxin Jiang

In this study, a series of novel p-menthane type secondary amines (sec-p-menthane-7-amine derivatives 3a–3y) were synthesized and then characterized by FTIR, 1H NMR, 13C NMR, and HRMS. The post-emergence herbicidal activities of these amines against barnyard grass and rape were evaluated by the culture dish method. Most of the sec-p-menthane-7-amine derivatives showed excellent herbicidal activities equivalent to or even higher than either diuron or glyphosate. The alkyl-substituted derivatives were more active than the phenyl-substituted derivatives. The herbicidal activities of compounds 3p, 3r, 3u, and 3w against the root growth of barnyard grass were 404% higher, respectively, than those of glyphosate. The herbicidal activities of compounds 3q, 3v, 3w, and 3x against the root growth of rape were 561%, 494%, 491%, and 544% higher, respectively, than those of diuron, and 484%, 760%, 423%, and 665% higher respectively, than those of diuron against shoot growth of rape. In addition, compounds 3p, 3u, and 3v are almost harmless to rice, wheat, sorghum, maize, and peanuts at a concentration of 100 mg L−1. Most of the compounds are nontoxic to HUVEC-C and BALB/c 3T3 cells. It is indicated that the title compounds could be utilized as botanical herbicides for future weed control.

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MICROPOROUS AND MESOPOROUS MATERIALS · 2023 · IF 5.2

Phosphorus promotion on hydrothermal stability of ZSM-5 by P precursors with different molecular sizes

Ne Ni,Xiuzhi Gao,Enhui Xing,Yuan Zhu,Jianqiang Liu,Mudi Xin,Ying Ouyang,Yibin Luo,Xingtian Shu

The promotional effects of phosphorous modification on ZSM-5 zeolites by phosphorus oxyacids (H 4 P 2 O 7 , H 3 PO 4 , H 3 PO 3 , and H 3 PO 2 ) with different molecular sizes were investigated with catalytic cracking of n -tetradecane as the probe reaction. It was verified that the diffusion of P precursor molecules into ZSM-5 channels was important to prevent aggregation of P species for better stabilization on tetra-coordinated framework aluminum . Meanwhile, the P–Al interaction was proposed based on results of 27 Al, 31 P, and 29 Si MAS NMR. With H 3 PO 2 as the P precursor, easy diffusion into ZSM-5 channels contributed to less formation of polyphosphates, homogeneous distribution of P species, better reserved crystallinity, microporous area and acidic sites for improving cracking performance of n -tetradecane.

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Polymers · 2020 ·Vol. 12 ·期 11 ·2482 · IF 3.426

Novel Temperature/Reduction Dual-Stimulus Responsive Triblock Copolymer [P(MEO2MA-co- OEGMA)-b-PLLA-SS-PLLA-b-P(MEO2MA-co-OEGMA)] via a Combination of ROP and ATRP: Synthesis, Characterization and Application of Self-Assembled Micelles

Fei Song,Zhidan Wang,Wenli Gao,Yu Fu,Qingrong Wu,Shouxin Liu

Novel temperature/reduction dual stimulus-responsive triblock copolymers, poly [2-(2-methoxyethoxy) ethyl methacrylate-co-oligo (ethylene glycol) methacrylate]-b-(L-polylactic acid)-SS-b-(L-polylactic acid)-b-poly[2-(2-methoxyethoxy) ethyl methacrylate-co-oligo(ethylene glycol)methacrylate] [P(MEO2MA-co-OEGMA)-b-PLLA-SS-PLLA-b-P(MEO2MA-co-OEGMA)] (SPMO), were synthesized by ring opening polymerization (ROP) of L-lactide and 2,2’-dithio diethanol (SS-DOH), and random copolymerization of MEO2MA and OEGMA monomers via atom transfer radical polymerization (ATRP) technology. The chemical structures and compositions of the novel copolymers were demonstrated by proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared spectroscopy (FTIR). The molecular weights of the novel copolymers were measured by size exclusive chromatography (SEC) and proved to have a relatively narrow molecular weight distribution coefficient (ÐM ≤ 1.50). The water solubility and transmittance of the novel copolymers were tested via visual observation and UV–Vis spectroscopy, which proved the SPMO had a good hydrophilicity and suitable low critical solution temperature (LCST). The critical micelle concentration (CMC) of the novel polymeric micelles were determined using surface tension method and fluorescent probe technology. The particle size and morphology of the novel polymeric micelles were characterized by dynamic light scattering (DLS) and transmission electron microscopy (TEM). The sol–gel transition behavior of the novel copolymers was studied via vial flip experiments. Finally, the hydrophobic anticancer drug doxorubicin (DOX) was used to study the in vitro release behavior of the novel drug-loaded micelles. The results show that the novel polymeric micelles are expected to become a favorable drug carrier. In addition, they exhibit reductive responsiveness to the small molecule reducing agent dithiothreitol (DTT) and temperature responsiveness with temperature changes.Keywords:temperature/reductive dual-stimulus responsiveness;block copolymers;amphiphilic;ring-opening polymerization;atom transfer radical polymerization

CAS / MDL: 26915-72-0 4511-42-6
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