Batteries-Basel
·
2023
·Vol. 9
·期 7
·352
·
IF 4
Xueqi Zhang,Ruilin Bian,Zhiyuan Sang,Shandong Tan,Ji Liang,Liqun Wang,Feng Hou
Aqueous zinc-ion batteries (ZIBs) have been regarded as a promising alternative to traditional lithium-based batteries due to their intrinsic advantages of safety, low cost, and abundance. However, the strong electrostatic interaction between Zn2+and the layer-structured cathodes is still a key issue that hinders the batteries from storing more Zn. Herein, we report partially nitrided and cation-doped vanadium oxide for improved Zn storage performance. Specifically, the defects and nitride species that are generated inside the material upon nitriding improve the conductivity of the material and introduce a new Zn storage mechanism. The intercalation of cations, in contrast, widens the interlayer spacing to store more Zn2+ions and enhances the cycling stability of the material. These merits synergistically lead to significantly enhanced electrochemical Zn2+ion storage performance, in terms of a high specific capacity of 418.5 mAh·g−1at a current density of 0.1 A·g−1and a capacity retention of 81.2% after 500 cycles at 2.0 A·g−1. The new modification strategy for V2O5suggested in this work could provide insight into the development of high-performance ZIBs.Keywords:aqueous zinc-ion batteries;cathode materials;vanadium oxide;partial nitridation;anion/cation co-doping
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CHROMATOGRAPHY A
·
2023
·
IF 4.1
Tianpei Cai,Xiaoyu Sun,Jia Chen,Hongdeng Qiu
In this work, tetraethylenepentamine (TEPA) was used as precursor and reaction medium to prepare tetraethylenepentamine-functionalized carbon dots (TEPACDs), the resultant mixture was subsequently silanized and then grafted on the surface of bare silica. The obtained tetraethylenepentamine-functionalized carbon dots and tetraethylenepentamine co-modified silica stationary phase (Sil-TEPA/CDs) was characterized by multiple ways, such as Fourier transformed infrared spectroscopy (FTIR), elemental analysis and transmission electron microscope, which revealed the successful preparation of the mixed stationary phase and higher density of functional groups on co-modified stationary phase than precursor single-modified stationary phase. The synergistic effect of TEPACDs and TEPA was proved by comparing the separation performance of Sil-TEPA/CDs and Sil-TEPA toward amino acids, nucleosides, and nucleobases, which distinctly enhanced the selectivity of Sil-TEPA/CDs. Thus, 12 nucleosides and nucleobases and 11 amino acids was nicely separated on Sil-TEPA/CDs. By study the influences of the changes of mobile phase composition, mobile phase buffer concentration and buffer pH on the retention behaviors of Sil-TEPA and Sil-TEPA/CDs, it was found that both hydrophilic partitioning and adsorption of analytes on Sil-TEPA/CDs were enhanced benefit from the co-existence of TEPA and TEPACDs, which provided the analytes better separation performance. By comparing the column quality of Sil-TEPA/CDs with four commercially available columns, Sil-TEPA/CDs exhibited the best peak asymmetry of 0.98, and second best column efficiency of 43895 m −1 using guanosine as analyte. The RSD ( n = 9) of the retention times of five selected analytes on Sil-TEPA/CDs were within 0.30–0.61% during 40 h of continuously elution, which implied excellent stability of prepared packing material.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Applied Nano Materials
·
2023
·
IF 5.9
Ning Chen,Shaohua Wei,Yongjun Feng,Shui Hu,Ying Tang,Wenqiang He,Yabin Zhang,Ding Cao,Zhifeng Fu
Electromagnetic absorbing materials (EMAs) are materials that irreversibly convert electromagnetic waves into another type of energy. With the development of communication technology, electromagnetic absorption materials have broad prospects in smart phones, wearable devices, and aerospace. MXenes have excellent dielectric loss properties, and the synthesis and application of MXene functional materials with magnetic properties will be one of the hotspots and focuses of future research. In this study, magnetic Co-Ti3C2Tx MXenes were prepared by molten salt etching, and Co-Ti3C2Tx/Fe2O3/polyacrylonitrile (PAN) hollow fiber composites with double-loss capability were prepared by coaxial electrospinning technology. The maximum reflection loss of the Co-Ti3C2Tx/Fe2O3/PAN hollow fiber can reach −54.62 dB at 9.86 GHz, and the effective absorption bandwidth is 6.39 GHz. The Co-Ti3C2Tx/Fe2O3/PAN hollow fibers with excellent electromagnetic absorption capability exhibit potential for efficient EMA materials due to their synergistic effect of impedance matching and magnetic/dielectric loss.
✓ 已验证
产品关联
DOI
高影响因子
Journal of Materials Chemistry B
·
2023
·Vol. 11
·期 26
·6147-6158
·
IF 7
Xiaoxi Song,Chun Zhang,Mengyuan Xing,Chunyan He,Dongxu Wang,Lijuan Chong,Xiuli Zhang,Minghui Chen,Jingjing Li
Photothermal therapy (PTT) is an effective and well-documented approach to thermally ablate tumors. However, the side effect of distal metastasis and recurrence limit its further expansion. At the same time as PTT was developed, the employment of imaging to monitor the treatment of tumors also became meaningful. Herein, as a proof of concept, gadolinium-doped mesoporous carbon nanoparticles (Gd-MCNs) were prepared as nanocarriers, MRI contrast agents, and PTT agents by a one-step hard template method, which realized Gd doping and carbon filling simultaneously, while retaining enough pore space for drug loading. After loading the immune adjuvant, R837, and the coating of tumor extracellular vesicle, the obtained biomimetic nanoparticles (EV@Gd-MCNs-R837) not only allowed tumor MRI, but also inhibited the primary tumor and its metastasis with long-term immune memory in vivo. This study provides proof for the potential of Gd-MCNs-based biomimetic nanoparticles for targeted PTT/immune-enhanced synergistic theranostic of tumors.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY
·
2022
·
IF 5.062
Dickson Pius Wande,Yue Qiu,Shijie Chen,Lan Yao,Yanghui Xu,Jing Yao,Hui Xiong
Oxaliplatin (OXA) and rapamycin (RAPA) combination therapy have shown the advantages of synergistically inhibiting the growth of cancer cells by enhancing apoptosis in cancerous cell lines. However, drug resistance and the lack of an orally administered formulation which exhibited the best clinical dosing compliance limited the clinical application of this regimen. Here, we report a nanogel-polymersomes drug delivery system (i.e.TMOR-CDAN) based on modified chitosan, chitosan diacetate (CDA), methoxy-poly-(ethylene glycol)-b-poly (lactide) (MPP), and D-alpha-tocopheryl polyethylene glycol succinate (TPGS) with permeation-glycoprotein (P-gp) inhibition capability for enhancing the oral chemotherapy efficacy of erroneously soluble RAPA and its synergistic chemotherapy with OXA. Hydrophilic OXA and hydrophobic RAPA were co-loaded using MPP and TPGS-based polymer capsules (i.e. TMOR), which were further coated by chitosan-modified gel to form TMOR-CDAN. The TMOR-CDAN displayed higher stability in both acidic and basic pH than free OXA and RAPA and could withstand the harsh gastric environmental conditions, preventing the burst drugs release while releasing the co-loaded drugs in a sustained and controlled manner. The dual-drug-loaded TMOR-CDAN provides a bifunctional platform for synergistic tumor therapy. Compared with the single drug OXA, RAPA, or the OXA and RAPA mixtures (OR), the TMOR-CDAN showed more outstanding in vitro cytotoxicity and in vivo antitumor chemotherapeutic efficacy, endowing the TMOR-CDAN with a prodigious potential for futuristic cancer chemotherapy .
✓ 已验证
产品关联
DOI
高影响因子
APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Zhuozheng Hong,Zili Xu,Zhengtao Wu,Hao Zhang,Ping Li,Xun Xu,Shuwang Duo
Tungsten-based nitrides are ideal hydrogen evolution reaction (HER) electrocatalysts owing to their Pt-like electronic structures, high electrical conductivity, and good corrosion resistance. However, the conventional preparation of tungsten-based nitride electrocatalysts suffers from environmentally hazardous sources and high-temperature nitridation processes, which usually restrict HER activity. Herein, we report the direct synthesis of W 2 N on metal–organic framework (MOF)-derived Co-NC microarrays using magnetron sputtering. Co-NC microarray support increased the number of surface activity sites that were exposed to W 2 N. Moreover, the formation of Co-NC@W 2 N Schottky heterojunctions significantly facilitated charge transfer between Co-NC and W 2 N. The Co-NC@W 2 N heterojunctions showed outstanding HER activity with an overpotential of 55 mV in reaching a current density of 10 mA cm −2 . Notably, Co-NC@W 2 N exhibited superior HER performance to Pt/C catalyst at high current densities. This study provides a simple and environmentally friendly approach for fabricating high-performance metal-nitride catalysts for water splitting.
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL RESEARCH IN CHINESE UNIVERSITIES
·
2022
·Vol. 38
·期 5
·1251-1257
·
IF 2.726
Li Yang,Wang Xian,Liu Jie,Jin Zhao,Liu Changpeng,Ge Junjie,Xing Wei
In this work, the effect of Nafion ionomer content on the structure and catalytic performance of direct CO polymer electrolyte membrane fuel cell(CO-PEMFC) by using Rh-N-C single-atom catalyst as the anode catalyst layers was studied. The ionic plaque and roughness of the anode catalyst layers increase with the increase of Nafion ionomer content. Furthermore, the contact angle measurement results show that the hydrophilicity of the anode catalyst layers also increases with the increase of Nafion ionomer content. However, when the Nafion ionomer content is too low, the binding between microporous layers, catalyst layers and membrane cannot meet the requirement for either electric conductivity or mass transfer. While Nafion ionomer content increased above 30%, the content of water in anode is difficult to control. Therefore, it was found that AN 30(30% Nafion ionomer content of anode) is the best level to effectively extend the three-phase boundary and improve CO-PEMFCs performance.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MEMBRANE SCIENCE
·
2022
·
IF 10.53
Yirong Sun,Jundong Zhong,Ziyu Lin,Ruiyin Sun,Liyuan Chen,Zhenhua Jiang,Jinhui Pang
Interfacial polymerization has always been a research hotspot for the preparation of polyamide (PA) membranes for molecular sieving. In previous reports, water-soluble amines (such as piperazine (PIP), m-phenylenediamine (MPD), etc.) were mostly used as monomers containing amino functional groups in the aqueous phase to conduct interfacial polymerization with 1,3,5-mesotribenzoyl chloride (TMC) in hexane , resulting in a dense PA film. However, this approach limits the diversity of polymer structures in PA films. To introduce water-insoluble 9,9-Bis(4-aminophenyl)fluorene (BAF) with a rigid twisted structure into interfacial polymerization, this study reports the interfacial polymerization of BAF in DMF/water solution with TMC in n-hexane. BAF-PA films with a larger free volume compared with MPD-PA were successfully prepared. The anomalous interfacial diffusion phenomenon was explained by the interfacial properties and molecular diffusion mechanism of the two-phase solvent and was confirmed by observing the microscopic morphology of the film. Since the structure of BAF-PA has a larger free volume, the BAF-PA film prepared by co-solvent interfacial polymerization has higher permeance to methanol (23.88 L m −2 h −1 bar −1 ). Meanwhile, it has more than 90% rejection of dyes with molecular weights of 585 Da and above. The large free volume PA film prepared with DMF/water mixed solvent exhibited excellent performance in organic solvent nanofiltration . This method also offers the possibility of introducing other water-insoluble amines into the interfacial polymerization to prepare PA films.
✓ 已验证
产品关联
DOI
高影响因子
Nature Communications
·
2022
·Vol. 13
·期 1
·1-10
·
IF 17.694
Wang Qiyou,Liu Kang,Hu Kangman,Cai Chao,Li Huangjingwei,Li Hongmei,Herran Matias,Lu Ying-Rui,Chan Ting-Shan,Ma Chao,Fu Junwei,Zhang Shiguo,Liang Ying,Cortés Emiliano,Liu Min
Atomically dispersed transition metals on carbon-based aromatic substrates are an emerging class of electrocatalysts for the electroreduction of CO 2 . However, electron delocalization of the metal site with the carbon support via d-π conjugation strongly hinders CO 2 activation at the active metal centers. Herein, we introduce a strategy to attenuate the d-π conjugation at single Ni atomic sites by functionalizing the support with cyano moieties. In situ attenuated total reflection infrared spectroscopy and theoretical calculations demonstrate that this strategy increases the electron density around the metal centers and facilitates CO 2 activation. As a result, for the electroreduction of CO 2 to CO in aqueous KHCO 3 electrolyte, the cyano-modified catalyst exhibits a turnover frequency of ~22,000 per hour at −1.178 V versus the reversible hydrogen electrode (RHE) and maintains a Faradaic efficiency (FE) above 90% even with a CO 2 concentration of only 30% in an H-type cell. In a flow cell under pure CO 2 at −0.93 V versus RHE the cyano-modified catalyst enables a current density of −300 mA/cm 2 with a FE above 90%.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ENVIRONMENTAL RESEARCH
·
2022
·
IF 8.431
Bin Wang,Qianyuan Mo,Bo Qin,Lei Song,Jiang Li,Guishang Sheng,Dezhi Shi,Xiaoyi Xu,Li'an Hou
The residual antibiotics detected frequently in aquatic environment may pose a potential threat to human health and ecosystem. Exploring a possible way to remove them from antibiotic polluted-water is a key problem demanding prompt solution. To investigate their adsorption characteristics, three antibiotics including tetracycline (TC), ciprofloxacin (CIP), and sulfadiazine (SDZ) have been removed using sucrose-based mesoporous carbon (SMC) in single and co-existing systems. Characterization revealed that the SMC had a high Brunauer-Emmett-Teller (BET) surface area (1215.48 m 2 /g), large mesoporous pore size (6.36 nm), and abundant oxygen-containing functional groups, which might offer sufficient adsorption sites for antibiotics. The process of antibiotics adsorption was described well using pseudo-second-order model. The rate constant K 2 at various temperatures followed the order 308 K > 298 K > 288 K. This finding suggesting the increase in temperature could promote the removal of antibiotics. The maximum adsorption capacities for TC (232.10 mg/g), CIP (257.30 mg/g), and SDZ (204.28 mg/g) of SMC were obtained using Langmuir isotherm (pH = 4–6, T = 308K, SMC dosage = 10 mg, C 0 = 30–40 mg/L). These data implied SMC had the excellent adsorptive property and affinity to antibiotics. In binary systems, SMC offers efficient removal percentages (>90%) for each of the target antibiotic. While the removal efficiencies of TC, CIP, and SDZ by SMC in the ternary system were 90.40, 72.99, and 80.46%, respectively. These results suggested the competition on active sites of SMC happened among the three antibiotics. The affinities of SMC to three antibiotics followed the order TC > SDZ > CIP. The removal of antibiotics by SMC were mainly attributed to the mechanisms including electrostatic interactions, hydrophobic interactions, hydrogen bonding and so on. This study will provide a technical support for antibiotic wastewater treatment .
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
·
2022
·
IF 7.129
Junjie Zhao,Yehui Luan,Yanan Chen,Linli Cheng,Qianxi Qin
Antibiotic residue has become an emerging environmental contaminant, while the toxicological effects and underlying mechanisms caused by the co-exposure to multiple veterinary antibiotics were rarely studied. In this study, male Sprague Dawley rats were exposed to monensin (M) (1, 2, 10 mg/(kg·body weight (BW)) combined with sulfamethazine (S) (60, 120, 600 mg/(kg·BW)) or single drugs for 28 consecutive days. The body weight, hematological and blood biochemical parameters, organ coefficients, and histopathology were analyzed to discover their combined toxicity effect. Transcriptomic analysis was used to reveal the possible mechanisms of their joint toxicity. Compared with the control group, the weight gain rate was significantly reduced in the H-M+S and H-S, and alkaline phosphatase in H-M+S was significantly increased. Furthermore, relative liver and kidneys weight was significantly increased, and the liver of H-M+S showed more severe lesions in histopathological analysis. For H-M+S, H-M and H-S, transcriptomic results showed that 344, 246, and 99 genes were differentially expressed, respectively. The Gene Ontology terms mainly differ in sterol biosynthetic process and steroid hydroxylase activity. The Kyoto Encyclopedia of Genes and Genome pathways showed abnormal retinol metabolism, metabolism of xenobiotics by cytochrome P450, and drug metabolism-cytochrome 450; the common 30 genes were screened from the network of protein-protein interaction. The results showed that mixed contamination of M and S produces hepatotoxicity by interfering with linoleic acid metabolism, retinol metabolism and CYP450 enzyme-dominated drug metabolism. Further analysis showed that Cyp1a2, Cyp2c61, Ugt1a3, and Ugt1a5 might be the key genes. These findings could provide more evidence for investigating the toxic effects and metabolism of mixed antibiotics contamination in mammals.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
MATERIALS CHEMISTRY AND PHYSICS
·
2022
·
IF 4.778
Xijun Li,Sifan Zhang,Lihua Zhu,Jun Liu,Huan Zhang,Ning Zhao,Bing Hui Chen
Herein, a series of the Pt-based bimetallic catalysts (PtM x /SBA-15) are gained by using ultrasonic incipient wetness impregnation method (M = Co, Cu, Ni or Zn). The experimental results show that the catalytic performance (including catalytic activity (turnover frequency-TOF), selectivity to crotyl alcohol) of PtCo x /SBA-15 for catalyzing crotonaldehyde selective hydrogenation is the best among PtM x /SBA-15. Additionally, the ratio of Pt/Co in the PtCo x /SBA-15 catalysts is changed to successfully synthesize PtCo/SBA-15, PtCo 2 /SBA-15, PtCo 5 /SBA-15. It demonstrates that the selectivity of the PtCo x /SBA-15 catalysts for crotonaldehyde selective hydrogenation to crotyl alcohol is significantly improved with the increase of the Co content. The PtCo 5 /SBA-15 catalyst provides 83.8% conversion of crotonaldehyde, 94.3% selectivity to crotyl alcohol and TOF of 910.5 h −1 under mild reaction conditions (3.0 MPa H 2 , 80 °C and 2.0 h). And PtCo 5 /SBA-15 has much better catalytic performance (higher catalytic activity and selectivity to crotyl alcohol) than PtCu 5 /SBA-15, PtNi 5 /SBA-15 and PtZn 5 /SBA-15. The reasons are as follows: (1) PtCo alloy forms, which is conducive to crotonaldehyde adsorption and activation; (2) there is an appropriate synergy effect between Pt and Co, greatly improving the capacity of the catalyst activating hydrogen under mild conditions; (3) the electron transfers from Co to Pt, resulting in the increase of Pt electron density and decrease of Co electron density, then the Co sites are advantageous to C O group adsorption and activation and Pt sites for H 2 adsorbing and activating; (4) with the increase of the Co proportion in PtCo x /SBA-15, the synergy effect between Pt and Co in PtCo alloy strengthens and thus increases the selectivity of C O group hydrogenation.
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）