Journal of Water Process Engineering
·
2023
·
IF 7
Jiaqi Wei,Yuanyuan Zhang,Jinxing Ma,Shanshan Wang,Minmin Jiang,Qiaoyan Wei,Mei Chen,Xiaowu Huang,Haixiang Li,Xuehong Zhang,Junjian Zheng
Degradation of refractory organics has been limited by their low mass-transport rates in conventional flow-by operated electrochemical reactors. This study explores for the first time the development of porous titanium (Ti)-based metal oxide anodic membrane for efficient flow-through degradation of recalcitrant tetrabromobisphenol A (TBBPA). For this purpose, a duplexed Ti/SnO 2 -Sb/PbO 2 -Ce anodic membrane was successfully prepared by sol-gel and electrodeposition methods. Ti/SnO 2 -Sb/PbO 2 -Ce exhibited improved mechanical and electrochemical stability, larger electrochemical surface area, higher oxygen evolution potential and lower charge transfer resistance, as compared to its mono-layered rival (Ti/SnO 2 -Sb). The switching from flow-by to flow-through operation resulted in an increased mass transfer rate constant and narrowed diffusion layer thickness of Ti/SnO 2 -Sb/PbO 2 -Ce. In the flow-through mode, Ti/SnO 2 -Sb/PbO 2 -Ce enabled the complete TBBPA removal at a relatively low electric energy (0.11 kWh m −3 ). The TBBPA removal was ascribed to the direct anodic oxidation and indirect anodic oxidation incurred by absorbed HO , free HO and 1 O 2 . The intermediate products, which were arisen from the attack of TBBPA by these reactive species, were identified. We further estimated their acute toxicities and bioaccumulation factors. This research proposed a robust electrochemical filtration approach for detoxification of TBBPA-contaminated water.
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Nanomaterials
·
2023
·Vol. 13
·期 18
·2579
·
IF 5.3
Yue Chang,Minmin Han,Yehui Ding,Huiyun Wei,Dawei Zhang,Hong Luo,Xiaogang Li,Xiongbo Yan
Effectively regulating and promoting the charge separation and transfer of photoanodes is a key and challenging aspect of photoelectrochemical (PEC) water oxidation. Herein, a Ti-doped hematite photoanode with a CoFe-LDH cocatalyst loaded on the surface was prepared through a series of processes, including hydrothermal treatment, annealing and electrodeposition. The prepared CoFe-LDH/Ti:α-Fe2O3photoanode exhibited an outstanding photocurrent density of 3.06 mA/cm2at 1.23 VRHE, which is five times higher than that of α-Fe2O3alone. CoFe-LDH modification and Ti doping on hematite can boost the surface charge transfer efficiency, which is mainly attributed to the interface interaction between CoFe-LDH and Ti:α-Fe2O3. Furthermore, we investigated the role of Ti doping in enhancing the PEC performance of CoFe-LDH/Ti:α-Fe2O3. A series of characterizations and theoretical calculations revealed that, in addition to improving the electronic conductivity of the bulk material, Ti doping also further enhances the interface coupling of CoFe-LDH/α-Fe2O3and finely regulates the interfacial electronic structure. These changes promote the rapid extraction of holes from hematite and facilitate charge separation and transfer. The informative findings presented in this work provide valuable insights for the design and construction of hematite photoanodes, offering guidance for achieving excellent performance in photoelectrochemical (PEC) water oxidation.
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PubMed
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CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Yangjie Fu,Kejie Zhang,Yi Zhang,Yanqing Cong,Qi Wang
Visible-light-active MR/NH 2 -MIL-125(Ti) homojunction was successfully synthesized via post-synthetic modification of NH 2 -MIL-125(Ti). A chromophore group (–MR) similar to the structure of methyl red, was introduced to partially replace the –NH 2 group. Using pure NH 2 -MIL-125(Ti) and MR-MIL-125(Ti) as control samples, the possible structural and optical changes were carefully studied. It was found that the lattice structure remained unchanged, while the specific surface area and band gap were in the order of NH 2 -MIL-125(Ti) > MR/NH 2 -MIL-125(Ti) > MR-MIL-125(Ti). Despite of these, MR/NH 2 -MIL-125(Ti) exhibited highest photocurrent response and lowest charge transfer resistance, which were associated with optimal photocatalytic performance. For the photocatalytic reduction of Cr(VI), the estimated rate constant on MR/NH 2 -MIL-125(Ti) was ca. 9 times and 3 times relative to that on NH 2 -MIL-125(Ti) and MR-MIL-125(Ti), respectively. Besides, 4.6 times rate enhancement can also be observed on the homojunction relative to physical mixture (MR/NH 2 -MIL-125(Ti)-PM). The boosted photocatalytic performance may be ascribed to promoted separation and transfer of photogenerated electron-hole pairs. The operating factors was optimized at acidic pH (2.0), lower catalyst dosage (0.1 g/L) and appropriate concentration of coexisting organics (2.0 mM) within the tested range. Furthermore, good stability both in photocatalytic performance and structure were also observed after 5 cyclic runs. Thus, this study report a facile way for the construction of visible-light-active MOFs, and provided a stable photocatalytic candidate for the disposal of Cr(VI)-containing wastewaters.
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ACS Applied Energy Materials
·
2020
·
IF 4.473
Fengkai Wu,Jiale Xie,Yue You,Zhengyu Zhao,Liuliu Wang,Xiaoying Chen,Pingping Yang,Yuelong Huang
The poor conductivity and sluggish kinetics of hematite (α-Fe2O3) limit its photoelectrochemical (PEC) performance. Herein, a cobalt metal–organic framework (Co-MOF) ultrathin overlayer is in situ-grown onto a Ti-doped hematite nanorod array via the chemical bath deposition. The optimal Co-MOF/Ti:Fe2O3 achieves a photocurrent density of 2.24 mA/cm2 at 1.23 V [vs reversible hydrogen electrode (RHE)], which is 2.4-folds that of pristine Fe2O3. When compared with the onset potential of Ti:Fe2O3, Co-MOF/Ti:Fe2O3 exhibits a cathodic shift of 310 mV. Co-MOF/Ti:Fe2O3 also shows a photocurrent density retention of 98.1% after the 6 h stability test. The improved PEC activity is mostly ascribed to the increased charge separation and surface charge injection. Ti doping increases the electron density in Fe2O3 and lowers the Fermi level (vs RHE), facilitating the charge transport in the bulk. The enhanced photovoltage and favorable distribution of surface states after Co-MOF modification and the catalytic/conductive properties of Co-MOF induce the enhanced charge separation/injection and the low onset potential.
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Bioactive Materials
·
2020
·
IF 8.724
Wei Xu,Chenjin Hou,Yuxuan Mao,Lei Yang,Maryam Tamaddon,Jianliang Zhang,Xuanhui Qu,Chaozong Liu,Bo Su,Xin Lu
When biomaterials are implanted in the human body, the surfaces of the implants become favorable sites for microbial adhesion and biofilm formation, causing peri-implant infection which frequently results in the failure of prosthetics and revision surgery. Ti–Mo alloy is one of the commonly used implant materials for load-bearing bone replacement, and the prevention of infection of Ti–Mo implants is therefore crucial. In this study, bacterial inhibitory copper (Cu) was added to Ti–Mo matrix to develop a novel Ti–Mo–Cu alloy with bacterial inhibitory property. The effects of Cu content on microstructure, tensile properties, cytocompatibility, and bacterial inhibitory ability of Ti–Mo–Cu alloy were systematically investigated. Results revealed that Ti–10Mo–1Cu alloy consisted of α and β phases, while there were a few Ti 2 Cu intermetallic compounds existed for Ti–10Mo–3Cu and Ti–10Mo–5Cu alloys, in addition to α and β phases. The tensile strength of Ti–10Mo-xCu alloy increased with Cu content while elongation decreased. Ti–10Mo–3Cu alloy exhibited an optimal tensile strength of 1098.1 MPa and elongation of 5.2%. Cytocompatibility study indicated that none of the Ti–10Mo-xCu alloys had a negative effect on MC3T3-E1 cell proliferation. Bacterial inhibitory rates against S. aureus and E. coli increased with the increase in Cu content of Ti–10Mo-xCu alloy, within the ranges of 20–60% and 15–50%, respectively. Taken together, this study suggests that Ti–10Mo–3Cu alloy with high strength, acceptable elongation, excellent cytocompatibility, and the bacterial inhibitory property is a promising candidate for biomedical implant applications.
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INTERNATIONAL JOURNAL OF REFRACTORY METALS & HARD MATERIALS
·
2020
·
IF 3.407
Zhaoran Chen,Dejiang Ma,Shanmin Wang,Wenhao Dai,Pinwen Zhu,Yiqing Zhu,Baochang Liu
Ti-coated diamond with different particle sizes and proper amounts of cubic boron nitride (cBN) was used to fabricate polycrystalline diamond composite (PDC) with improved wear resistance and thermal stability under high temperature and high pressure (5.5–6.5GPa, 1500–1650 °C). The ratio of Ti-coated diamond powder, cBN powder and normal diamond powder was W 30 – 50 : W 4 – 8 : W 0 – 1 = 70: 15: 15. Cobalt (Co) was used as a binder, and cemented tungsten carbide was used as a substrate to sinter a new high-performance PDC. Ti and TiC on the surface of Ti-coated diamond reacted with cBN under high temperature and high pressure to generate new ceramic phases such as TiB 2 , TiN and TiN 0.3 , which have high hardness and good wear resistance. Compared with the conventional PDC, the impact toughness and wear resistance of PDC with Ti-coated diamond and cBN addition were enhanced by 19% and 28%, respectively. The ceramic phase acts as a protective barrier, which enhances the initial graphitization and oxidizing temperature to 942–950 °C, which were 162–170 °C higher than the conventional PDC. The new ceramic barrier wrapped around the surface of the diamond and Co after the formation of the D-D (diamond-diamond) bonding will give priority to the oxidation reaction of Co and diamond with oxygen, which prohibits cobalt-catalytic graphitization of diamond, meeting the needs of PDC thermal stability and wear resistance in the field of drilling.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 13
·D638
·
IF 3.12
Pengfei Xu,Xiaohong He,Junwei Mao,Yongming Tang
In this paper, Ti/SnO2-Sb/Ce-PbO2 anode is electrodeposited from MSA bath, and the effect of Ce3+ concentration in bath on the phase composition and morphology of lead dioxide electrode is elucidated. It is found that with the addition of 2 mM Ce3+ ion to the bath the Ce-PbO2 anode exhibits highest stability in 0.5 M H2SO4, and cerium exists as Ce (IV) in the PbO2 film. The electrocatalytic activity of lead dioxide anode for phenol removal is slightly enhanced by the inclusion of Ce. The significant improvement in electrocatalytic activity can be achieved by the addition of small amount of Bi3+ ion to the bath containing Ce3+ ion. In this study, electrocatalytic activities of various anodes follow the order: Ce,Bi-PbO2 > Ce-PbO2 > undoped PbO2 > Bi-PbO2.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
·
2019
·Vol. 30
·期 16
·15097-15104
·
IF 2.195
Mi Yijin,Zhao Hui,Jia Dongling,Miao Yuqing
Bosk-like Co–Sn–Se monocrystals are deposited on porous Ti plate through a hydrothermal method. The prepared Co–Sn–Se was characterized with morphology, composition and electrocatalytic properties. Electrochemical measurements revealed that the Ti/Co–Sn–Se electrodes exhibited great catalytic performance for hydrogen evolution reaction with the low onset overpotential of − 50 mV, the small Tafel slope of 83 mV/dec and good stability over an extended period of 34,000 s. The high electrocatalytic activity of bosk-like Co–Sn–Se monocrystals, the fast electron transfer between electrodes and catalysts, and the high conductivity of Ti contribute to their acceptable electrocatalytic performance.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2019
·Vol. 166
·期 13
·E401
·
IF 3.12
Handong Jiao,Shuqiang Jiao,Wei-Li Song,Haosen Chen,Mingyong Wang,Jiguo Tu,Daining Fang
Owing to the low-cost and fast process, molten salt electrolysis is considered as a novel method to replace the Kroll process for preparing titanium. However, this process has not been fully realized because of the multi-step reduction and complicated disproportionation behaviors of multivalent titanium ions in melt. To address such critical problems, here we use liquid metals (Sn and Pb) as the cathode instead of solid metal cathode (Mo) during the electrolysis, in which the reduction process of Ti3+ (TiF63−) becomes a simple one-step process (Ti3+ + 3e = Ti (alloys)). Also, the deposition potential is more positive (>0.5 V) than that using solid Mo, owing to the depolarizing effect of the liquid metals. One-step process and depolarization behavior are favorable to increase the current efficiency, effectively decreasing the power consumption in comparison with the conventional electrolysis at solid metal cathodes. Similar to the electrolytic production of aluminum in Hall-Heroult system, there would be a continuous electrolysis process because the product is liquid alloy in this system.
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CHEMICAL ENGINEERING JOURNAL
·
2019
·
IF 8.355
Jun Pan,Kang Yu,Hongzhi Mao,Lili Li,Yuchen Zhang,Yanlu Li,Paulo J. Ferreira,Jian Yang
A simple synthesis has been developed for watermelon-like nanocomposites with Ti-based oxides as the matrix. Using the case of Sb nanocrystals in amorphous TiPO x as an example, in-situ/ex-situ techniques, first-principle calculations and control experiments confirm that the formation of Ti-based oxides promotes the reduction of Sb 3+ to Sb by NH 3 at an elevated temperature. A similar synthesis process also succeeds for Sb nanocrystals in amorphous TiO 2 and for Bi nanocrystals in amorphous TiPO x , confirming the promising potential of this synthesis. More importantly, the nanocomposite composed by crystalline Sb in an amorphous TiPO x matrix, as the anode material for sodium storage, concurrently exhibits a long cycle life (~1000 cycles) and a high capacity retention (~82%), suggesting the advantages of watermelon-like structures.
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Journal of Materials Chemistry A
·
2018
·Vol. 6
·期 48
·24860-24868
·
IF 9.931
Hao Chen,Chunlong Dai,Yanan Li,Renming Zhan,Min-Qiang Wang,Bingshu Guo,Youquan Zhang,Heng Liu,Maowen Xu,Shu-juan Bao
Hybrid ion capacitors, especially sodium ion capacitors (SICs), have recently attracted enormous attention due to their combined merits of high energy density from the battery-type anode and high power density from the capacitor-type cathode. However, achieving high-performance SICs to overcome the sluggish kinetic energy storage feature and inferior cycling stability of the battery-type anode remains a challenge. In this work, N-doped porous carbon embedded with ultrasmall titanium oxynitride nanoparticles (TiOxNy/C) was developed from metal–organic frameworks (MOFs). As the SIC anode, the as-designed TiOxNy/C exhibited a high reversible capacity (275 mA h g−1 at 50 mA g−1), ultrahigh rate capability, and superior cycling performance, which is attributed to the effective synergy between the ultrasmall TiOxNy nanoparticles and N-doped porous carbon. Furthermore, using a “two-for-one” strategy, N-doped hierarchical porous carbon (NHPC) with high surface area was prepared from TiOxNy/C by HF etching and displayed high specific capacity and rate capability when used as a SIC cathode. Considering the excellent electrochemical performances of both the anode and cathode, the as-assembled TiOxNy/C//NHPC SIC delivered a high energy density (80 W h kg−1) and high power density (4000 W kg−1).
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Micro & Nano Letters
·
2018
·Vol. 13
·期 10
·1373-1377
·
IF 0.841
Hui Zhao,Yuqing Miao
The Ni–W–S nanoparticles (NPs) were synthesised on Ti mesh through the typical hydrothermal method. The obtained Ti/Ni–W–S was characterised on morphology, composition and electrocatalytic property. It showed good electrocatalytic performance towards glucose oxidation in strong alkali electrolyte, exhibiting the potential application in the field of fuel cell. The excellent electrocatalytic activity of Ni–W–S NPs, the favourable electron transfer between electrode and catalysts, as well as the high conductivity of Ti contributed to its final catalytic performance of Ti/Ni–W–S.
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