ANALYTICA CHIMICA ACTA
·
2023
·
IF 6.2
Yuanyuan Zhang,Yuan Zhu,Tianjing Zeng,Lu Qiao,Mingjuan Zhang,Kexin Song,Nian Yin,Yani Tao,Yue Zhao,Chang Zhang,Yi Zhang
A highly sensitive photoelectrochemical aptasensor based on phosphorus-doped hollow tubular g-C 3 N 4 /Bi/BiVO 4 (PT-C 3 N 4 /Bi/BiVO 4 ) for tobramycin (TOB) detecting was developed. This aptasensor is a self-powered sensing system which could generate the electrical output under visible light irradiation with no external voltage supply. Based on the surface plasmon resonance (SPR) effect and unique hollow tubular structure of PT-C 3 N 4 /Bi/BiVO 4 , the PEC aptasensor exhibited an enhanced photocurrent and favorably specific response to TOB. Under the optimized conditions, the sensitive aptasensor presented a wider linearity to TOB in the range of 0.01–50 ng mL −1 with a low detection limit of 4.27 pg mL −1 . This sensor also displayed a satisfying photoelectrochemical performance with optimistic selectivity and stability. In addition, the proposed aptasensor was successfully applied to the detection of TOB in river water and milk samples.
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高影响因子
CHEMOSPHERE
·
2023
·
IF 8.8
Litao Jia,Chenjia Yang,Xiaoyong Jin,Dan Wang,Fanghua Li
A hot research topic in visible-light-driven photoelectrocatalytic (PEC) oxidation technology is the development of superior photoanode materials. The design of the photoanode system with a direct Z-scheme charge transfer mechanism is crucial to achieving effective charge separation for sustainable photoelectrocatalysis. Here, a novel Bi / Bi 2 S 3 /α-MoO 3 heterostructure was successfully assembled by a simple and feasible strategy. The direct Z-scheme heterogeneous formed between Bi 2 S 3 and α-MoO 3 has the advantages of low resistance, high optical response current and the surface plasmon resonance (SPR) effect of Bi nanoparticles (Bi NPs). Thus, the efficiency of photogenerated carrier separation and transfer is further enhanced, and the catalytic activity is significantly improved. It is impressive that the unique photoanode has achieved a maximum removal efficiency of 85.8% of tetracycline (TC) pollutants under visible light irradiation within 60 min and has excellent stability, which is expected to degrade antibiotics efficiently and environmentally in harsh environments. These characteristics give Bi / Bi 2 S 3 /α-MoO 3 promising candidates for practical applications in antibiotic degradation.
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Journal of Materials Chemistry B
·
2023
·Vol. 11
·期 6
·1240-1261
·
IF 7
Po Zhang,Jialin Chen,Yuzhi Sun,Zhicheng Cao,Yanan Zhang,Qingyun Mo,Qingqiang Yao,Wei Zhang
Osteochondral defect (OCD) regeneration remains a great challenge. Recently, multilayer scaffold simulating native osteochondral structures have aroused broad interest in osteochondral tissue engineering. Here, we developed a 3D multifunctional bi-layer scaffold composed of a kartogenin (KGN)-loaded GelMA hydrogel (GelMA/KGN) as an upper layer mimicking a cartilage-specific extracellular matrix and a hydroxyapatite (HA)-coated 3D printed polycaprolactone porous scaffold (PCL/HA) as a lower layer simulating subchondral bone. The bi-layer scaffolds were subsequently modified with tannic acid (TA) prime-coating and E7 peptide conjugation (PCL/HA-GelMA/KGN@TA/E7) to regulate endogenous stem cell behaviors and exert antioxidant activity for enhanced osteochondral regeneration. In vitro, the scaffolds could support cell attachment and proliferation, and enhance the chondrogenic and osteogenic differentiation capacity of bone marrow-derived mesenchymal stem cells (BMSCs) in a specific layer. Besides, the incorporation of TA/E7 significantly increased the biological activity of the bi-layer scaffolds including the pro-migratory effect, antioxidant activity, and the maintenance of cell viability against oxidative stress. In vivo, the developed bi-layer scaffolds enhanced the simultaneous regeneration of cartilage and subchondral bone when implanted into a rabbit OCD model through macroscopic, micro-CT, and histological evaluation. Taken together, these investigations demonstrated that the 3D multifunctional bi-layer scaffolds could provide a suitable microenvironment for endogenous stem cells, and promote in situ osteochondral regeneration, showing great potential for the clinical treatment of OCD.
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高影响因子
Advanced Electronic Materials
·
2023
·Vol. 10
·期 3
·2300651
·
IF 6.2
Tianpeng Yu,Shuyi Hou,Zhenliang Liu,Yiru Wang,Jiang Yin,Xu Gao,Nannan Liu,Guoliang Yuan,Lei Wu,Yidong Xia,Zhiguo Liu
Organic field-effect transistors (OFETs) hold great promise for applications in non-volatile memories, detectors, and artificial synapses due to the good flexibility and biocompatibility. However, certain drawbacks such as high operating voltages and significant degradation in endurance characteristics have hindered their practical implementations. Herein, a novel approach is proposed to enhance the performance of OFETs by incorporating a bi-functional n-type polymer semiconductor interlayer, Poly-{[N,N'-bis(2-octyldodecyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)} (N2200), into a pentacene OFET structure. The device exhibits remarkable improvements, with reliable P/E operation cycles of over than 10 4 and a retention time of more than 10 years. On one hand, the inclusion of N2200 as an n-type semiconductor effectively reduces the height of hole-injection barrier for trapping and thus reducing the working voltage based on the electrostatic induction theory. On the other hand, n-type semiconductor N2200 serves as a native hole-consumption (or hole-trapping) dielectric, and its narrower bandgap restrains the formation of deep hole-traps, thus favoring the endurance characteristics of the OFET.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2023
·
IF 9.9
Jiahao Chen,Miao He,Anjun Hu,Mengjiao Liu,Chuan Zhao,Bo Zhou,Runjing Li,Zhongfu Yan,Yu Pan,Yining Fan,Jing Liu,Liujun Cao,Jianping Long
Rechargeable aqueous zinc-ion hybrid supercapacitors (ZHSs) are drawing extensive attention because of their cost-effectiveness and diminished safety hazards. Nevertheless, large-scale application of ZHSs has been hindered by the severe side reactions and rampant dendrites growth on the surface of Zn metal anodes. Herein, we propose a three-dimensional organic–inorganic composite frame material as an artificial bi-functional layer coated on the zinc foil, featuring nitrogenous functional groups with zincophilicity (abbreviated as NCFM@Zn). The nitrogen (N) site's strong adsorption capacity and synergistic effect of the sub-nanopore size promote rapid desolvation of zinc ions and reduce side reactions, while also prolonging galvanized nucleation's Sand's time and allowing for even nucleation. Moreover, the uniform distribution of N on the layer results in homogeneous zinc ions flux and supports consistent zinc plating while inhibiting dendrites generation. As a result of this unique artificial bi-functional layer, symmetric Zn cells can survive 2500 h at 2.5 mA cm −2 . High-areal-capacity zinc||activated carbon hybrid supercapacitors also demonstrate 20,000 cycles at high Coulombic efficiency, thus highlighting the utter convenience and potential of this strategy for modifying rechargeable metal hybrid supercapacitor surfaces.
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APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Hongjing Tian,Jin Du,Peng Lu,Shengnan Xu,Yanxia Guo,Jixing Tang,Man Wu,Qingjie Guo
A novel solid bi-amine adsorbent was synthesized by simultaneously impregnating pentaethylenehexamine (PEHA) and aminoethylethanolamine (AEEA) on the surfaces of mesoporous MCM–41 nanospheres. AEEA and PEHA had a synergistic effect during the CO 2 adsorption of the bi-amine adsorbent and the highest CO 2 adsorption capacity was 4.03 mmol·g −1 . The bi-amine adsorbent exhibited the favorable recyclability because its saturated CO 2 adsorption capacity decreased by 6.20 % after the initial eight adsorption/desorption cycles while by only 2.23 % in the following seven cycles. The adsorption activation energy and the desorption activation energy were determined to be 12.53 and 16.81 kJ·mol −1 , respectively. The low value of the desorption activation energy suggested an inconsiderable energy requirement in the multicycles of the adsorbent. The characterization results indicated that hydrogen bonds were formed between the hydrogen atom in hydroxyl groups of AEEA and the oxygen atom in carbonyl groups of the carbamate. The synergistic effect between AEEA and PEHA was unveiled on the CO 2 adsorption of the bi-amine adsorbent. The formed hydrogen bonds facilitated the release of protons from carbamic acids, enhanced the stability of the produced carbamate anions, and thus boosted the CO 2 adsorption performance.
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ChemNanoMat
·
2022
·Vol. 9
·期 1
·e202200400
·
IF 3.82
Bo Zhu,Xu Lu,Jiadang Li,Wenhao Xie,Lifei Wang,Qiang Zhang,Jianfeng Fan,Yun Zheng
Graphical The substitution of iso-valent Bi for Sb is adopted to adjust the thermoelectric transport properties of the undoped Mg 3 Sb 2 compound. The improved power factor and figure of merit are obtained accordingly. Bismuth is the most common alloying element for high-performance Mg 3 Sb 2 -based thermoelectric compounds. However, the electrical and thermal transport data is lacking for undoped Mg 3 (Sb, Bi) 2 solid solutions. In this study, theoretical calculation results show that Bi alloying can reduce the band gap of Mg 3 Sb 2 , favoring the regulation of carrier concentration. Both Mg 3 Sb 2 and Mg 3 SbBi compounds present a single band structure on the valence band maximum at Γ of the Brillouin zone. Incorporating the Bi element can slightly increase the density of states (DOS) on the valence band maximum, which is beneficial for the Seebeck coefficient. Mg 3 Sb 2-x Bi x (0≤x≤0.8) compounds were experimentally prepared via ball milling (BM) combined with the spark plasma sintering (SPS) technique. The carrier concentration, electrical conductivity, and power factor of the samples tend to increase with the increasing Bi content. Bismuth alloying significantly reduces the total thermal conductivity in the low-temperature range, with the lowest value of 0.65 Wm −1 K −1 obtained at ∼400 K for the x=0.2 sample. The peak ZT value of 0.077 at 800 K and the average ZT of 0.051 in the temperature range of 450–800 K are obtained for the x=0.2 sample, which is 93% and 219% higher than those of the unalloyed sample, respectively. This work reveals the Bi-alloying induced transport mechanism and provides fundamental thermoelectric data regarding the undoped Mg 3 Sb 2-x Bi x (0≤x≤0.8) solid solutions.
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JOURNAL OF MEMBRANE SCIENCE
·
2022
·
IF 10.53
Jian Lu,Bingang Xu
In recent years, molecularly imprinted membrane (MIM) has exhibited superiority in industrial separation, drug purification, solid-phase extraction and even medical detection owing to its remarkable selectivity. For catechins, however, the reactivity with free radicals limits the traditional construction of MIM towards such molecules. Here in this work, we have developed a bio-inspired MIM towards Epigallocatechin gallate (EGCG, a representative catechin) by the anchoring/imprinting strategy. The covalent interactions based on boronate-affinity supplied an oriented anchoring effect, while the non-covalent interactions from l -cysteine promoted the formation of imprinted sites that are highly matched with template. Mild and efficient imprinting was carried out by self-polymerization of dopamine to avoid the destruction of templates. As a result, remarkable selectivity coefficients (2.70 and 4.58), permselectivity coefficients (more than 3.19 and 3.41) and separation factors (5.18 and 7.00) were achieved on the EGCG-imprinted membrane (EIM), accompanied by the impressive imprinting factor (10.14) and superior regeneration performance (only 4.4% of the decline in five cycles). For deep insight into selective recognition and separation, microscopic and visualized mechanisms of site formation and specific rebinding was proposed by molecular dynamics simulations. Approaches with such an anchoring/imprinting strategy will enrich the avant-garde molecular imprinting strategies, and also expand membrane-based applications.
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CARBOHYDRATE POLYMERS
·
2022
·
IF 10.723
Weifeng Xu,Xiang Liu,Kewen Tang
A novel bi-functional β-cyclodextrin polymer (CD@TCT@PEI) was synthesized for the removal of hydroquinone and Pb(II) from wastewater. The structure and adsorption performance of CD@TCT@PEI towards hydroquinone and Pb(II) were studied comprehensively. Both of the adsorption processes fit the pseudo-second-order kinetic model well. The adsorption isotherms of hydroquinone and Pb(II) could be described well by Langmuir isotherm model, and the maximum adsorption capacities of hydroquinone and Pb(II) are 364.86 and 113.52 mg g −1 , respectively. The adsorption of hydroquinone and Pb(II) on CD@TCT@PEI is an exothermic and spontaneous process. The adsorbed CD@TCT@PEI could be regenerated easily, and can still maintain high adsorption performance after 5 cycles. The electrostatic interaction and coordination interaction account for the adsorption of Pb(II), and inclusion of cyclodextrin and hydrogen-bond interaction are responsible for hydroquinone adsorption. This study provides some insights to design an adsorbent that can simultaneously remove heavy metal ions and organic micropollutants from wastewater.
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高影响因子
INORGANICA CHIMICA ACTA
·
2022
·
IF 3.118
Huimin Huang,Yuandong Wu,Shuangsheng Cheng,Shaoguo Wen,Yi Qu,Thomas Doert,Dajiang Mei
A new bismuth(III) complex [(1,10-phen)Bi(C 2 O 4 ) 1.5 ], 1,10-phen = 1,10-phenanthroline, was synthesized with oxalate and phen ligands without by-products. The title complex was characterized by single crystal X-ray diffraction, FT-infrared Spectrum, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). 2D bismuth - oxalate - bridged layers are formed by oxalate ligands. Phen ligands are embedded in it which further stabilize the structure. The luminescence properties show that [(1,10-phen)Bi(C 2 O 4 ) 1.5 ] can emit blue-green fluorescence, and π - π stacking and ligand-to-metal-charge transfer (LMCT) are predominant in it, which may have potential applications in the fields of crystal luminescent materials.
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY
·
2022
·
IF 6.76
Junfeng Yang,Yuyang Wu,Yanhui Dong,Hao Cui,Chenyang Shi,Hang Sun,Shengyan Yin
Herein, a ternary Bi@H-TiO 2 /B-C 3 N 4 type II heterostructure is successfully designed and prepared via metal Bi as cocatalyst for photocatalytic H 2 generation. As expected, under λ > 300 nm light, the highest photocatalytic hydrogen production rate (HPR) of Bi@H-TiO 2 /B-C 3 N 4 is up to 223.08 μmol g −1 h −1 . Excitingly, under visible light (λ > 400 nm), the highest HPR of Bi@H-TiO 2 /B-C 3 N 4 is increased to 18.84 μmol g −1 h −1 , which is about 67.3 times, 37.7 times and 6.8 times as high as that of H-TiO 2 , B-C 3 N 4 and H-TiO 2 /B-C 3 N 4 under the same conditions, respectively. Moreover, the electrochemical impedance spectroscopy and transient photocurrent tests manifest that the interface resistance of Bi@H-TiO 2 /B-C 3 N 4 composite decreases and the photocurrent density increases after loading metal Bi. These results indicate that loading metal Bi as cocatalyst (providing more electron trapping sites) is beneficial to improve photocatalytic activity in the type II heterostructure composite. And the electron transfer directions (B-C 3 N 4 → H-TiO 2 → Bi or B-C 3 N 4 → Bi) are proved by ultraviolet photoelectron spectroscopy test. Therefore, the Bi@H-TiO 2 /B-C 3 N 4 photocatalyst with strong visible light absorption is expected to be a promising candidate in photocatalytic fields under visible light.
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E-POLYMERS
·
2022
·Vol. 22
·期 1
·468-477
·
IF 3.074
Lin Chen,Ye Sun,Jiawen Wang,Chao Ma,Shuyi Peng,Xingyu Cao,Lang Yang,Chunxin Ma,Gaigai Duan,Zhenzhong Liu,Hui Wang,Yihui Yuan,Ning Wang
Although diverse uranium (U) adsorbents have been explored, it is still a great challenge for high-efficient uranium extraction form seawater. Herein a wood-mimetic oriented porous Ti 3 C 2 T
x
-MXene/gelatin hydrogel (MGH) has been explored through growing directional ice crystals cooled by liquid nitrogen and subsequently forming pores by freeze-dry (Ice-template) method, for ultrafast and high-efficient U-adsorption from seawater with great enhancement by both electric field and sunlight. Different from disperse Ti 3 C 2 T
x
-MXene powder, this MGH not only can be easily utilized but also can own ultrahigh specific surface area for high-efficient U-adsorption. The U-adsorbing capacity of this MGH (10 mg) can reach 4.17 mg·g −1 after only 1 week in 100 kg of seawater, which is outstanding in existing adsorbents. Furthermore, on the positive pole of 0.4 V direct current source or under 1-sun irradiation, the U-adsorbing capacity of the MGH can increase by 57.11% and 13.57%, respectively. Most importantly, the U-adsorption of this hydrogel can be greatly enhanced by simultaneously using the above two methods, which can increase the U-adsorbing capacity by 79.95% reaching 7.51 mg·g −1 . This work provides a new biomimetic porous MXene-based hydrogel for electric field/sunlight bi-enhanced high-efficient U-extraction from seawater, which will inspire new strategy to design novel U-adsorbents and systems.
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危险品化学品经营许可证（带存储）