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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

Boosted lithium storage cycling stability of TiP2 by in-situ partial self-decomposition and nano-spatial confinement

Fengchen Zhou,Xu-Sheng Yang,Jiangwen Liu,Jun Liu,Renzong Hu,Liuzhang Ouyang,Min Zhu

Titanium phosphide (TiP 2 ) is particularly interesting due to its ability to form the stable Li–Ti–P ternary phase. However, TiP 2 faces the limitations in cyclic stability due to the volume change occurred by the destruction/recovery of the long-range cubic order Li–Ti–P phase, and unable to deliver high capacity. In this work, we propose the in-situ formation of electrochemically inactive TiP and phosphorus via partial decomposition of TiP 2 by ball milling process, achieving a multi-phase TiP 2 –TiP–P–C composite. On one hand, the decomposition-formed TiP effectively relieve the stress caused by the formation of Li x TiP 4 and LiP 3 . On the other hand, another decomposition-formed small-sized phosphorus significantly reduce its volume change during the lithiation/delithiation cycles for the overall capacity. Accordingly, the synthesized multi-phase TiP 2 –TiP–P–C with the above cooperative effects delivers a high capacity of 836.3 mAh g −1 at 0.2 A g −1 as high-performance Lithium-ion battery anode. In addition, a notable capacity retention of 81.4% is also achieved after 1000 cycles at 5 A g −1 . Furthermore, when paired with LiFePO 4 cathode in a full cell, the excellent specific capacity, cycling and rate performance can also be obtained. The rational design of TiP 2 –TiP–P–C will be beneficial towards the future development of metal-phosphide-phosphorous composite as LIB anode.

CAS / MDL: 7723-14-0 7440-32-6
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MACROMOLECULAR BIOSCIENCE · 2020 ·Vol. 21 ·期 1 ·2000194 · IF 3.416

Smart Titanium Coating Composed of Antibiotic Conjugated Peptides as an Infection-Responsive Antibacterial Agent

Yunfei Zhang,Kuan Hu,Xuan Xing,Jingshuang Zhang,Ming-Rong Zhang,Xiaohui Ma,Rui Shi,Liqun Zhang

Antibacterial coating is rapidly emerging as a pivotal strategy for mitigating spread of bacterial pathogens. However, many challenges still need to be overcome in order to develop a smart coating that can achieve on-demand antibacterial effects. In this study, a Staphylococcus aureus ( S. aureus ) sensitive peptide sequence is designed, and an antibiotic is then conjugated with this tailor-made peptide. The antibiotic-peptide conjugate is then linked to the surface of a titanium implant, where the peptide can be recognized and cleaved by an enzyme secreted by S. aureus . This allows for the release of antibiotics in the presence of S. aureus , thus achieving delivery of an antibacterial specifically when an infection occurs.

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Materials · 2020 ·Vol. 13 ·期 23 ·5356 · IF 3.057

Formation Mechanism of High-Purity Ti2AlN Powders under Microwave Sintering

Weihua Chen,Jiancheng Tang,Xinghao Lin,Yunlong Ai,Nan Ye

In the present study, high-purity ternary-phase nitride (Ti2AlN) powders were synthesized through microwave sintering using TiH2, Al, and TiN powders as raw materials. X-ray diffraction (XRD), differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) were adopted to characterize the as-prepared powders. It was found that the Ti2AlN powder prepared by the microwave sintering of the 1TiH2/1.15Al/1TiN mixture at 1250 °C for 30 min manifested great purity (96.68%) with uniform grain size distribution. The formation mechanism of Ti2AlN occurred in four stages. The solid-phase reaction of Ti/Al and Ti/TiN took place below the melting point of aluminum and formed Ti2Al and TiN0.5phases, which were the main intermediates in Ti2AlN formation. Therefore, the present work puts forward a favorable method for the preparation of high-purity Ti2AlN powders.Keywords:MAX-phase Ti2AlN;microwave;synthesis;high-purity powder

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RARE METALS · 2020 ·Vol. 40 ·期 7 ·1940-1948 · IF 2.161

Oxidation behavior of multi-component Ta–W–Al–Ti alloy at 1173 K

Li Jia-Xin,Chen Yu-Hong,Bai Zhang-Jun,Zhao Bao-Jun,Jiang Liang,Wu Lan-Er

Ta–W alloys have unique properties but their applications at high temperatures are restricted due to their poor oxidation resistances. The addition of Al and Ti decreases the oxidation rate of the alloy, as Al-contained protective oxide layer could be formed. In this study, ternary and quaternary Ta–W alloys containing Al and Ti were prepared by hot press sintering. The microstructures and oxidation behaviors of the alloys were studied at 1173 K. The results show that the oxidation kinetics of all alloys follows a parabolic law at short oxidation periods. After cyclic oxidation, the kinetics of quaternary alloys still obeys the parabolic law but that of ternary alloy has been changed into linear law kinetics after 8-h oxidation. For ternary alloy, an outer layer with dense and continuous alumina was formed during the initial stage, and phase transformation caused the oxides to peel off. By comparison, the quaternary alloys depicted continuously solid solution of the oxides layer. Overall, Al and Ti played key roles in oxidation degree and affected the oxidation kinetics of ternary and quaternary alloys.

CAS / MDL: 7440-32-6
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Journal of Advanced Dielectrics · 2020 · IF 0

Macroporous 3D MXene architecture for solar-driven interfacial water evaporation

Maomao Ju,Yawei Yang,Jianqiu Zhao,Xingtian Yin,Yutao Wu,Wenxiu Que

Interfacial water evaporation through solar heating with photothermal materials is a promising strategy for seawater desalination and wastewater purification. Tightly packed 2D membranes with high reflection losses and limited vapor escape channels result in a low evaporation rate. In this work, 3D MXene architecture was fabricated by dropping the delaminated Ti 3 C 2 ( d d -Ti 3 C 2 ) nanosheets onto the carbonized melamine foam (CMF) framework. Owing to the macroporous 3D architecture, more effective broadband solar absorption and vapor escaping were achieved. As a result, the 3D CMF@ d d -Ti 3 C 2 -based evaporator delivers a water evaporation rate of 1.60 kg/m 2 ⋅ ⋅ h with a solar-to-vapor conversion efficiency of up to 84.6%.

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Nature Communications · 2020 ·Vol. 11 ·期 1 ·1-10 · IF 12.121

Irreversible accumulated SERS behavior of the molecule-linked silver and silver-doped titanium dioxide hybrid system

Zhou Lu,Zhou Jun,Lai Wei,Yang Xudong,Meng Jie,Su Liangbi,Gu Chenjie,Jiang Tao,Pun Edwin Yue Bun,Shao Liyang,Petti Lucia,Sun Xiao Wei,Jia Zhenghong,Li Qunxiang,Han Jiaguang,Mormile Pasquale

In recent years, surface-enhanced Raman scattering (SERS) of a molecule/metal–semiconductor hybrid system has attracted considerable interest and regarded as the synergetic contribution of the electromagnetic and chemical enhancements from the incorporation of noble metal into semiconductor nanomaterials. However, the underlying mechanism is still to be revealed in detail. Herein, we report an irreversible accumulated SERS behavior induced by near-infrared (NIR) light irradiating on a 4-mercaptobenzoic acid linked with silver and silver-doped titanium dioxide (4MBA/Ag/Ag-doped TiO 2 ) hybrid system. With increasing irradiation time, the SERS intensity of 4MBA shows an irreversible exponential increase, and the Raman signal of the Ag/Ag-doped TiO 2 substrate displays an exponential decrease. A microscopic understanding of the time-dependent SERS behavior is derived based on the microanalysis of the Ag/Ag-doped TiO 2 nanostructure and the molecular dynamics, which is attributed to three factors: (1) higher crystallinity of Ag/Ag-doped TiO 2 substrate; (2) photo-induced charge transfer; (3) charge-induced molecular reorientation.

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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Ti3C2Tx//AC dual-ions hybrid aqueous supercapacitors with high volumetric energy density

Yapeng Tian,Chenhui Yang,Yi Tang,Yangyang Luo,Xiaojie Lou,Wenxiu Que

Supercapacitors with an advanced high volumetric energy density require a match of both electrodes materials and suitable electrolyte. Here, aqueous asymmetric supercapacitors are designed by employing layered Ti 3 C 2 T x as negative electrodes and highly compact activated carbon (AC) as positive electrodes. Ti 3 C 2 T x //AC asymmetric supercapacitors (Ti 3 C 2 T x //AC ASCs) with 1.7 V voltage window are designed by regulating the mass ratio of both electrodes, which results from the shift of the open circuit potential with different applied voltages. Then, dual-ion hybrid supercapacitors (Ti 3 C 2 T x //AC-KBr HSCs) are also constructed by introducing redox active (KBr) into traditional electrolyte (H 2 SO 4 ) for Ti 3 C 2 T x //AC ASCs to achieve a high volumetric energy density, in which fast hydronium ion intercalated pseudocapacitance happens at the Ti 3 C 2 T x negative electrode, while redox reaction of Br − /Br 3 − within the highly compact AC happens at the positive electrode. As a result, the Ti 3 C 2 T x //AC-KBr HSC achieves a high volumetric capacitance of 250 F cm −3 at 2 mV s −1 , a volumetric energy density of as high as 102.8 Wh L −1 at 424 W L −1 and an outstanding cycling stability with 122% capacitance retention after 6000 cycles. Furthermore, the self-discharge performance for the Ti 3 C 2 T x //AC-KBr HSC is obviously improved, which is mainly ascribed to the adsorption of oxidized species at the AC surface.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2020 · IF 4.65

Size-dependent effects of Ti powders in the pure aluminum matrix composites reinforced by carbon nanotubes

X.Q. Liu,C.J. Li,X. You,Z.Y. Xu,X. Li,R. Bao,J.M. Tao,J.H. Yi

Carbon nanotube reinforced aluminum matrix (CNT/Al) composites with various microstructures were fabricated by powder metallurgy via introducing nano-sized and micron-sized Ti powders into the CNT-Al system. The size-dependent effects of Ti powders on the microstructure evolution and mechanical properties were further investigated. The results reveal that the best enhancement (∼51% of UTS) was obtained by adding 80 nm sized Ti powders into the CNT/Al composite compared with the composite without Ti addition, which mainly derives from the synergistic strengthening of the homogenously dispersed CNTs, a large quantity of in-situ formed nano-sized TiAl 3 particles and fine grains. Meanwhile, it is also noted that the addition of micron-sized Ti powders can help the CNT dispersion in powder fabrication stage, and subsequently in-situ formed core-shell structured particles with different interface reaction degree in the Al matrix. Among them, 1 μm was determined to be the optimal size of Ti for the maximum formation of core-shell structured particles, which best exploits the load transfer ability of TiAl 3 shell layers at their interfaces, and finally attributes to significant strength enhancement (∼35% of UTS). This research provides a valuable reference concerning the size effects of addition metal in future fabrication of CNTs reinforced metal matrix composites with alternative microstructure.

CAS / MDL: 7440-32-6
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INTERNATIONAL JOURNAL OF REFRACTORY METALS & HARD MATERIALS · 2020 · IF 3.407

Annealing induced shrinkage-fill effect of tungsten‑potassium alloys with trace titanium doping

Longqing Chen,Wenbin Qiu,Hao Deng,Xiaoliang Yang,Yangyipeng Song,Jun Zhu,Jun Tang

The shrinkages presented in sintering process of tungsten alloys are extremely detrimental to their practical applications in fusion reactors. Positively in this work, we effectively reduced the shrinkages via synergistically applying Ti-doping and annealing process on tungsten‑potassium (WK) alloys. This shrinkage-fill effect only works in the one with trace amount of titanium doping, such as 0.05 wt%Ti or 0.5 wt%Ti. Due to such effect, the compressive strength was improved by ~18%. Based on morphological and elementary analyses, we speculated that the Ti-rich particles along the grain boundaries of WK alloys were activated and migrated into shrinkages during annealing. Further Ti doping (e.g. 1wt.%Ti) led to nanoscale grain refinement in WK alloys, which almost doubled the compressive strength. In this case, an unconventional grain-refinement model was proposed. Furthermore, anomalous grain growth was observed in WK-3wt.%Ti, which was attributed to the formation of Ti-rich regions and the corresponding raise of energy in grain boundaries. The fabricating strategies in this work may benefit the design of refractory tungsten alloys with less shrinkages and ultra-fine grains.

CAS / MDL: 7440-32-6
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JOURNAL OF POWER SOURCES · 2020 · IF 8.247

A long cycle life asymmetric supercapacitor based on advanced nickel-sulfide/titanium carbide (MXene) nanohybrid and MXene electrodes

Yangyang Luo,Chenhui Yang,Yapeng Tian,Yi Tang,Xingtian Yin,Wenxiu Que

To enhance rate and cycle performances of nickel sulfide, the two-dimensional (2D) titanium carbide (Ti 3 C 2 , MXene) with good electrical conductivity and electrochemical stability is chosen as 2D supporting matrix for synthesizing nickel sulfide/delaminated Ti 3 C 2 (Ni–S/d-Ti 3 C 2 ) nanohybrids by a solvothermal method . The Ni–S/d-Ti 3 C 2 nanohybrids show a coexistence of Ni 3 S 2 and NiS with the characteristic peak of d-Ti 3 C 2 nanosheets , and have electroactive species-on-sheet structures. The optimal Ni–S/1d-Ti 3 C 2 nanohybrid delivers a high specific capacity of 840.4 C g −1 at 1 A g −1 with enhanced capacity retention of 64.3% at 30 A g −1 and an outstanding cycle performance, which are ascribed to an integration of d-Ti 3 C 2 nanosheets that can act as electric channels to accelerate electrons transport at interface of the nanohybrid during charge-discharge processes. An increased Ni 2+ content and BET surface area also contribute to redox reactions of Ni–S/1d-Ti 3 C 2 nanohybrid electrode. An asymmetric supercapacitor (ASC) fabricated by using the Ni–S/1d-Ti 3 C 2 nanohybrid as positive electrode and d-Ti 3 C 2 film as negative electrode exhibits an energy density of 20.0 Wh kg −1 at 0.5 kW kg −1 and a good cycling stability. Our work provides a favorable ingenuity for synthesizing advanced nickel sulfide-based nanohybrids and an alternative strategy of using 2D MXene as capacitive electrode for high-performance supercapacitors .

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ANALYTICA CHIMICA ACTA · 2020 · IF 5.977

Enhancement anti-interference ability of photoelectrochemical sensor via differential molecularly imprinting technique demonstrated by dopamine determination

Qi Kang,Qiao Zhang,Lixin Zang,Mengru Zhao,Xiaolan Chen,Dazhong Shen

Molecularly imprinting polymers (MIPs), as artificial antibodies with high recognition selectivity to template molecules, are widely used in various biosensors . To improve further the selectivity of MIPs-based photoelectrochemical (PEC) biosensors, we report a differential strategy using non-imprinted polymers (NIPs) as the reference. In a proof-to-concept example for the determination of dopamine (DA), MIPs and NIPs membranes were fabricated by electrochemical polymerization of polypyrrole membranes on the surface of graphene quantum dots (GQDs)/TiO 2 nanotubes (NTs). The photocurrent difference between the two PEC cells , MIPs@GQDs/TiO 2 NTs−Pt and NIPs@GQDs/TiO 2 NTs−Pt, was measured as the signal. As the non-specific adsorption of non-template molecules on the outside surface of MIPs and NIPs membranes is similar, the anti-interference ability for the determination of DA is much improved by using differential strategy. In the normal and differential PEC measurement models, 10.0 μM ascorbic acid is equivalent to 3.12 and 0.40 μM DA, respectively. Further, the smaller specific surface area in NIPs membrane was compensated by using a weight factor to correct the residual interference in a modified differential model. By using 10.0 μM ascorbic acid as the balance point, the presence of 10.0 μM H 2 O 2 , glutathione , uric acid or glucose is equivalent only to 0.090, 0.061,0.11 or 0.041 μM of DA, respectively, which are about 3–7% of their interference levels in the normal photocurrent model. The differential PEC method was applied in the determination of DA in serum samples in the linear range of 0.05–12.5 μM, with the detection limit of 0.018 μM.

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Journal of Oceanology and Limnology · 2020 ·Vol. 38 ·期 5 ·1517-1531 · IF 0.617

Photoelectrochemical cathodic protection of Cu2O/TiO2 p-n heterojunction under visible light

Tian Jing,Chen Zhuoyuan,Jing Jiangping,Feng Chang,Sun Mengmeng,Li Weibing

The Cu 2 O/TiO 2 p-n heterojunction composite photoelectrodes were prepared by depositing Cu 2 O nanoparticles on the surface of TiO 2 nanotubes via anodic oxidation and constant current deposition. Field emission scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) analyses showed that Cu 2 O nanoparticles not only deposited on the surface of TiO 2 nanotube array, but also on the wall of TiO 2 nanotubes. The Cu 2 O deposition amount could be adjusted by changing the deposition time. The photoelectrochemical cathodic protection (PECCP) performance of the prepared photoelectrodes for 316L stainless steel (SS) was tested under visible light. The constant current deposition time had a significant effect on the PECCP performance of Cu 2 O/TiO 2 -X photoelectrodes and Cu 2 O/TiO 2 -20 had the best PECCP performance for the coupled 316L SS. This was attributed to the appropriate amount and thickness of Cu 2 O to form p-n heterojunctions with TiO 2 , in which separation of the photogenerated carriers was accelerated and transfer of the photogenerated electrons to 316L SS for PECCP was facilitated.

CAS / MDL: 7440-32-6
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