ACS Sustainable Chemistry & Engineering
·
2017
·
IF 5.951
Miao Kan,Xufang Qian,Taiyang Zhang,Dongting Yue,Yixin Zhao
Here we report a highly active electrochemical water splitting electrode fabricated from colloidal IrOx nanoparticles and nanoporous Si stabilized by conformal TiO2. The colloidal amorphous IrOx nanoparticles are highly active for oxygen evolution reaction. However, their application for water splitting has a dilemma that the traditional annealing process could lead to low activities but the nanoparticles based electrode without annealing usually exhibited low stability. This nanostructured water splitting electrode exhibited both the high activities as the colloidal IrOx nanoparticles and comparable stability as a traditional thermal annealing fabricated electrode. The impedance study revealed that conformal TiO2 significantly inhibits the interface oxidation and maintains the high activity of colloidal IrOx nanoparticles catalysts. The conformal TiO2 interface engineering combined with nanocatalysts would be a promising strategy to achieve balanced activities and stability for water splitting.
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Nanoscale
·
2017
·Vol. 9
·期 43
·16764-16772
·
IF 7.367
Yayun Hong,Chenlu Pu,Hongli Zhao,Qianying Sheng,Qiliang Zhan,Minbo Lan
In this work, we fabricated a yolk–shell magnetic composite that contains mesoporous TiO2 as the inner shell and flowerlike NiO as the outer shell (denoted as Fe3O4@H-TiO2@f-NiO) to reduce the limitations of single-component metal oxides in phosphopeptide enrichment. The NiO nanosheets play a synergistic role in phosphopeptide enrichment. And the unique flowerlike structure of NiO with sufficient space can facilitate the reversible insertion/extraction of peptides, which will have less impact on the enrichment process of the inner TiO2 shell. The yolk–shell structure and two types of porous nanostructures endowed this composite with a high surface area (156.58 m2 g−1) and a large pore volume (0.37 cm3 g−1). Owing to the high surface area and combined properties of TiO2 and NiO, the Fe3O4@H-TiO2@f-NiO microspheres showed a better performance for phosphopeptide enrichment than the same material without NiO nanosheets (Fe3O4@H-TiO2). According to the LC-MS/MS results, 972 unique phosphopeptides were identified from HeLa cell extracts with a high selectivity (91.9%) by Fe3O4@H-TiO2@f-NiO relative to 837 phosphopeptides (selectivity: 60.2%) by Fe3O4@H-TiO2. The results demonstrated that, compared with single-component metal oxides, composite metal oxides could enhance the selectivity and sensitivity for phosphopeptide enrichment.
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JOURNAL OF THE ELECTROCHEMICAL SOCIETY
·
2017
·Vol. 164
·期 13
·H863
·
IF 3.259
Xingzhi Wang,Zhuang Wang,Xishun Jiang,Miao Zhang,Yanfen Wang,Jianguo Lv,Gang He,Zhaoqi Sun
Highly ordered TiO2 nanorod (TNR) arrays decorated with Cu2ZnSnS4 (CZTS) nanocrystals were prepared via a facile and effective method. The TNR arrays were synthesized using a hydrothermal treatment, and the CZTS nanocrystals were deposited by a three-step successive ionic layer adsorption and reaction (SILAR) technique followed by annealing in a sulfur atmosphere. The morphology, structure, composition, optical, and the photoelectrochemical (PEC) properties of the CZTS/TNR arrays were investigated in detail. The results demonstrate that the CZTS/TNR arrays can effectively facilitate photoinduced carrier transport, reduce the recombination rate of electron-hole pairs, and as a result demonstrate improved light absorption properties and PEC performance. The CZTS/TNR arrays sensitized with 7 SILAR cycles showed a maximal photocurrent density of 2.17 mA/cm2 at 0 V and the longest electron lifetime of 47.39 ms, which is nearly 80 and 2.03 times higher than those of pure TNR, respectively. The improvement in performance can be attributed to the high absorption coefficient and narrow bandgap of CZTS and the type-II nanoheterostructures with a staggered alignment of band edges present at the heterointerface. Surface passivation with ZnS resulted in a further improvement in PEC performance in comparison to the untreated CZTS/TNR arrays with values of 2.53 mA/cm2 and 59.77 ms for the maximal photocurrent density and longest electron lifetime, respectively.
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PARTICLE & PARTICLE SYSTEMS CHARACTERIZATION
·
2016
·Vol. 34
·期 3
·1600323
·
IF 4.367
Liwei Zhao,Hongbo Xu,Bo Jiang,Yudong Huang
Recently, there is crucial interest in the design and fabrication of nanocatalysts for efficient decomposition of organic pollutants in wastewater using visible light. This work reports the assembling fabrication of synergetic photocatalytic Au/TiO 2 /RGO nanostructures by utilizing the reduced graphene oxide (RGO) as substrate material and efficient separator for electrons and holes. The Au/TiO 2 nanostructures with a ≈7 nm TiO 2 particles size are dispersed uniformly on RGO nanosheets. UV–vis diffuse reflectance spectroscopy verifies that Au/TiO 2 /RGO nanocomposites show strong absorption of visible light. The degradation efficiency after 1 h for hydroquinone under visible light and UV light is ≈77% and ≈90%, respectively. Under visible light, the calculated apparent rates ( k ) of the Au/TiO 2 /RGO nanocomposites are 0.0112 and 0.0174 min −1 for decomposition of methylene blue and hydroquinone. That are five times greater than that of bare TiO 2 . The high photocatalytic activity is mainly attributed to the synergy between RGO and Au/TiO 2 nanostructure. The strategy of composite nanostructures assembling on RGO is ensured to have a great practicable potential for the designing of high efficient multielement composite nanoparticles catalysts.
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MATERIALS RESEARCH BULLETIN
·
2014
·
IF 1.968
Shu-Mei Zhou,De-Kun Ma,Ping Cai,Wei Chen,Shao-Ming Huang
Photocatalysts with excellent photocatalytic reaction activity and ideal selectivity are highly desirable for pollutants clearance and purification of targeted organics from a mixture. Continued efforts toward the goal, we here present a facile hydrothermal route to synthesize TiO 2 /Bi-benzenedicarboxylate/BiOCl nanoparticles decorated ultrathin nanosheets with a thickness less than 5 nm on a large scale. The as-synthesized products showed excellent photocatalytic activities for the degradation of various dyes such as rhodamine B, eosin Y and methylene blue in aqueous solution under visible light irradiation. The photocatalytic activities of TiO 2 /Bi-benzenedicarboxylate/BiOCl nanocomposites for the degradation of rhodamine B and eosin Y could be adjusted through tuning the content of TiO 2 . With increasing the amount of TiO 2 , the composites showed declining photocatalytic activities in decomposing of rhodamine B while on the contrary they displayed enhanced photocatalytic activities in decomposing of eosin Y. Interestingly, TiO 2 /Bi-benzenedicarboxylate/BiOCl composite nanosheets showed obvious photocatalytic selectivity in a mixed dyes system. The photocatalytic reaction and selectivity mechanisms of the nanocomposites for the degradation of the dyes were discussed on the basis of experimental results. The current study not only develops a new methodology to synthesize ultrathin nanosheets but also provides a novel strategy to design composite photocatalysts with high reaction activity and good selectivity.
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Nanoscale
·
2015
·Vol. 7
·期 41
·17488-17495
·
IF 7.394
Zuyang Zheng,Zhibin Fang,Xinxin Ye,Xiaobin Yao,Xianzhi Fu,Sen Lin,Ping Liu
Surface oxygen vacancy has been investigated extensively due to its great influence on photocatalysis in recent years. Among these investigations, the location of surface defects is found to be a key factor during the photocatalytic procedure. Especially when a crystal facet is involved, the synergistic action between these two factors may greatly increase the photocatalytic efficiency. Location of defects would greatly help in understanding the mechanism of this coupling action. Without an available technique, however, it is very difficult to gain the position information directly. In this paper, we provide a low-cost and visualized method to solve this problem via in situ reduction of Au. TiO2 with surface oxygen vacancy on a specific area is synthesized via a photochemical reaction. Then the Au ion was reduced at the place where oxygen vacancy exists on the TiO2 surface. Hence, the localization of surface vacancy will be determined by examining the location of Au particles. Moreover, application of this method can be extended to other surface defects such as oxygen vacancy on oxide semiconductors, Ti3+ in TiO2, Zn vacancy on ZnO, etc. This technique is helpful for understanding how surface defects affect the properties of semiconductors.
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SCIENCE OF THE TOTAL ENVIRONMENT
·
2014
·
IF 3.163
Bin Xia,Bijuan Chen,Xuemei Sun,Keming Qu,Feifei Ma,Meirong Du
The toxicity of TiO 2 engineered nanoparticles (NPs) to the marine microalga Nitzschia closterium was investigated by examining growth inhibition, oxidative stress and uptake. The results indicated that the toxicity of TiO 2 particles to algal cells significantly increased with decreasing nominal particle size, which was evidenced by the 96 EC 50 values of 88.78, 118.80 and 179.05 mg/L for 21 nm, 60 nm and 400 nm TiO 2 particles, respectively. The growth rate was significantly inhibited when the alga was exposed to 5 mg/L TiO 2 NPs (21 nm). Measurements of antioxidant enzyme activities showed that superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) activities were first induced and subsequently inhibited following exposure to 5 mg/L TiO 2 NPs. The depletion of antioxidant enzymes with a concomitant increase in malondialdehyde (MDA) levels and reactive oxygen species (ROS) posed a hazard to membrane integrity. A combination of flow cytometry analysis, transmission electron microscopy and Ti content measurement indicated that TiO 2 NPs were internalized in N. closterium cells. The level of extracellular ROS, which was induced by TiO 2 NPs under visible light, was negligible when compared with the intracellular ROS level (accounting for less than 6.0% of the total ROS level). These findings suggest that elevated TiO 2 nanotoxicity in marine environments is related to increased ROS levels caused by internalization of TiO 2 NPs.
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Journal of Physical Chemistry C
·
2015
·
IF 4.772
Yuangang Li,Rongrong Wang,Huajing Li,Xiaoliang Wei,Juan Feng,Kaiqiang Liu,Yongqiang Dang,Anning Zhou
Co-Pi decorated TiO2@graphitic carbon nitrides (g-C3N4) nanorod arrays (denoted as CCNRs) with different mass ratios of g-C3N4 have been constructed on the FTO substrate through three processes, hydrothermal growth, chemical bath deposition and electrodeposition. First, TiO2 nanorod arrays were grown onto a FTO substrate by a hydrothermal method. Second, g-C3N4 was coated onto the TiO2 nanorod arrays by immersing the above substrate with TiO2 nanorod arrays into a solution of urea and then heated at higher temperature. In this procedure, the amount of the g-C3N4 on the TiO2 nanorod arrays can be controlled by tuning the concentration of the urea solution. At last, Co-Pi were decorated on the surface of the TiO2@g-C3N4 by electrodeposition. The as-prepared CCNRs were characterized by XRD, FESEM, TEM, XPS, UV–vis, and FTIR, respectively, which illustrated that Co-Pi moieties were successfully decorated on the hybrid TiO2@g-C3N4 nanorod arrays. Photoelectrochemical (PEC) measurements have demonstrated that the prepared CCNRs serve as an efficient and stable photoanode for PEC seawater splitting. The photocurrent density reaches 1.6 mA/cm2 under 100 mW/cm2 (AM1.5G) light illumination at 1.23 V (RHE). More significantly, the CCNRs photoanode is quite stable during seawater splitting and the performance remain undiminished even after 10 h continuous illumination. Finally, a systematical photocatalytic mechanism of the Co-Pi decorated TiO2@g-C3N4 was proposed, and it can be considered as potential explanation of enhanced PEC performance.
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高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2014
·
IF 2.93
Junxian Wang,Jie Huang,Haolong Xie,Ailan Qu
A photocatalyst composed of graphite-like carbon nitride (g-C 3 N 4 ) and TiO 2 was fabricated by a simple method to calcine the mixture of melamine and TiO 2 precursor. The photocatalyst has enhanced photoactivity for hydrogen evolution from water. Characterization by XRD , FTIR, SEM and elemental analysis showed that the crystal structure and morphologies of composites were affected by the amount of melamine in the composite. The UV–Vis characterization displayed that the optical absorption range of g-C 3 N 4 /TiO 2 hybrid was broadened with a synergistic effect . The photoactivity for H 2 evolution was shown that the best result obtained from the composite with 67 wt% melamine has about 5 times improvement compared with bare TiO 2 or pure g-C 3 N 4 . The enhanced photoactivity might be related with the favorable structure resulted from heat-treatment temperature, and the content of g-C 3 N 4 participating in wide optical absorption, separation and transportation of electronic-holes, as well as morphology of composite.
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高影响因子
CARBON
·
2014
·
IF 6.16
Jianbing Zhu,Xiao Zhao,Meiling Xiao,Liang Liang,Changpeng Liu,Jianhui Liao,Wei Xing
The exploration of advanced catalyst supports is a promising route to obtain electrocatalysts with high activity and durability. Herein, the nitrogen-doped graphitized carbon/TiO 2 composite was fabricated and explored as support for the Pt catalyst. The composite support was constructed by carbonization of polypyrrole/TiO 2 using cobalt nitrate and nickel nitrate as graphitizing catalysts. The resulting catalyst shows enhanced electrocatalytic performance for methanol electrooxidation compared with the commercial Pt/C catalyst. The enhancement can be ascribed to combinatory effect of N-doped graphitized carbon and TiO 2 , in which the tolerance to CO-poisoning and the intrinsic kinetics of methanol oxidation reaction were simultaneously improved by the bifunctional effect and the modification of the electronic structure. As a result, the as-developed nitrogen-doped graphitized carbon/TiO 2 composite present attractive advantages for the application in fuel cell electrocatalyst.
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Journal of Materials Chemistry A
·
2013
·Vol. 2
·期 7
·2071-2078
·
IF 0
Lin Zhang,Dengwei Jing,Xilin She,Hongwei Liu,Dongjiang Yang,Yun Lu,Jian Li,Zhanfeng Zheng,Liejin Guo
The formation of heterojunctions is an efficient strategy to extend the light response range of TiO2-based catalysts to the visible light region. In addition to the bandgap edge match between the narrow bandgap semiconductors and the TiO2 substrate, a stable phase interface between the sensitiser and TiO2 is crucial for the construction of heterojunctions, since it acts as a tunnel for the efficient transfer of photogenerated charges. Herein, the coincidence site density (1/Σ) of graphite-like carbon nitride (g-C3N4) nanoflakes and two types of TiO2 nanofibres [anatase and TiO2(B)] was calculated by near coincidence site lattice (NCSL) theory. It was found that the coincidence site density of g-C3N4 and TiO2(B) nanofibre with an exposed (001) plane is 3 times of that of the g-C3N4 and anatase nanofibre with exposed (100) plane. This indicated that the g-C3N4 nanoflakes are more favoured to form stable heterojunctions with TiO2(B) nanofibres. As expected, a stable phase interface was formed between the plane of (22–40) of g-C3N4 and the plane (110) of TiO2(B) which had same d-spacing of 0.35 nm and the same orientation. Under visible light irradiation, the photogenerated electrons could efficiently migrate to the TiO2(B) nanofibres from the g-C3N4 through the heterojunctions. So the g-C3N4/TiO2(B) system exhibited better photodegradation ability for sulforhodamine B (SRB) dye than the g-C3N4/anatase system, although the photoactivity of the anatase nanofibres was much better than that of the TiO2(B) nanofibres.
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JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2014
·
IF 3.552
Yaru Ni,Wei Wang,Wenjuan Huang,Chunhua Lu,Zhongzi Xu
A new idea was employed to simultaneously reduce graphene oxide (GO) and wrap it on the surface of high-reactive anatase TiO 2 for fabricating novel TiO 2 -graphene (GP) hybrid materials. The process was based on the surface negatively charged property of GO. With the introduction of strong chemical interaction between TiO 2 and GP, the GP wrapped TiO 2 gives a strong red-shift of the light absorption edge and a further narrowed bandgap compared to that of GP randomly supported TiO 2 . This structure can also significantly enhance the separation efficiency of photogenerated electrons and holes. Furthermore, in contrast to the normal anatase TiO 2 , as-prepared TiO 2 is dominated with the high-reactive {0 0 1} facet. The superiority of the formed “core–shell” structure is confirmed by photocatalytic degradation of methylene blue (MB) under the xenon lamp and visible light irradiation. New photocatalytic mechanisms are also proposed based on the obtained results. This work may open a new doorway for new significant application of GP to prepare more GP-based high-reactive photocatalysts for environmental protection.
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