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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2022 · IF 4.598

Oxygen vacancies and Bi2S3 nanoparticles co-sensitized TiO2 nanotube arrays for enhanced photoelectrochemical sensing of chlorpyrifos

Jiawen Wu,Panpan Ou,Yu Lin,Xuecai Tan,Fucun Wei,Yan Mi,Shaogang Liu,Kejing Huang

Due to the environmental pollution and food safety problems that caused by the abuse of chlorpyrifos (CPF), a strategy of which is detected with high efficiency is urgently demanded. Herein, a photoelectrochemical sensor which using TiO 2 nanotube arrays with oxygen vacancies (V o -TNTAs) as electrode was constructed. Oxygen vacancies are introduced into TNTAs in order to generate a new defect level that narrows its band gap. The bismuth sulfide nanoparticles are loaded on V o -TNTAs to accelerate the separation of electron-hole pairs. Thus, the Bi 2 S 3 /V o -TNTAs hetero-structure is designed and constructed. With the existence of CPF, a complex which composed by Bi ions and CPF will be formed in situ to block the electrons transfer from electron donor (ascorbic acid) to Bi 2 S 3 , causing the weakened photocurrent. Consequently, the Bi 2 S 3 /V o -TNTAs electrode possess higher photocurrent response than that of pure V o -TNTAs and TNTAs. The Bi 2 S 3 /V o -TNTAs-based PEC sensor displays a linear range of 0.07–3.0 μmol/L with a detection limit of 6.0 nmol/L (S/N = 3) and can be utilized for CPF detection in lettuce and cucumber samples with recoveries of 95.7 to 110 %.

研究领域: 环境科学 · 分析化学
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Nanoscience and Nanotechnology Letters · 2018 ·Vol. 10 ·期 1 ·51-59 · IF 2.917

TiO2 Nanotube Photonic Crystals Coupled with Gold Nanoparticles for Efficient Visible-Light-Driven Photocatalysis

Guo Min,Yang Lu,Zhang Jun,Su Haijun,Liu Lin,Chen Jia,Fu Nianqing

To achieve highly efficient visible-light photocatalysis, a new composite photocatalyst was designed and constructed for the first time in this study by coupling novel TiO2 nanotube photonic crystals (TiO2 NT PCs) with localized surface plasmon resonance (LSPR) of gold nanoparticles (Au NPs). Due to the synergistic effect of slow photon and LSPR which originated from TiO2 NT PCs and Au NPs respectively, the photocatalyst could expand the light absorption spectrum, thus enhancing photocatalysis efficiency in the visible light region. Compared to its bare TiO2 NT and TiO2 NT PC counterparts, the optimized Au NPs/TiO2 NT PC showed superior performances under the visible light irradiation. Moreover, over 65% Rhodamine B was degraded within 3.5 h by the optimized Au NPs/TiO2 NT PC, while only 15% and 8% Rhodamine B were degraded within the same time by using Au NPs/TiO2 NT and bare TiO2 NT, respectively. We believe that this work will be helpful in designing of PC-coupled plasmonic nanostructure materials for visible-light-driven photocatalysts, as well as other photoelectronic applications, such as photoelectrochemical water splitting and photovoltaic.

研究领域: 材料科学 · 光催化技术 · 纳米科技
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JOURNAL OF ELECTROANALYTICAL CHEMISTRY · 2024 · IF 4.1

Exploring well-defined TiO2 nanotube arrays for enhancing SnO2-Sb-Nd-Pt electrode performance

Yang Li,Hairun Ma,Wenyu Xie,Jiahao Liang,Min Li,Shaohui Guo,Guangxu Yan

The short service life and low catalytic activity of electrodes are the major bottlenecks limiting the practical applications of current electrocatalytic oxidation technology in wastewater treatment. In this study, a novel Ti/SnO 2 -Sb-Nd-Pt electrode loading TiO 2 nanotube (TiO 2 -NTs) array was proposed and prepared. The optimized TiO 2 nanotube (TiO 2 -NTs) arrays provided abundant anchoring sites for SnO 2 -Sb-Nd-Pt active coating and improved the bonding strength between the Ti matrix and the SnO 2 -Sb-Nd-Pt active coating as a mediator, as a result, higher electrocatalytic performance and stability. The nitrobenzene (NB) removal and service life were significantly higher in Ti/TiO 2 -NTs/SnO 2 -Sb-Nd-Pt (91.08 % and 4381.9 days) when compared to Ti/SnO 2 -Sb-Nd-Pt (80.61 % and 1151.2 days). In addition, the outstanding electrocatalytic performance of Ti/TiO 2 -NTs/SnO 2 -Sb-Nd-Pt with an oxygen evolution potential of 2.03 V and total voltametric charge of 5.88 mC cm −2 makes it a promising candidate for future industrial applications. These findings will lay a solid foundation for broadening the applications of well-defined TiO 2 -NTs arrays prepared via the two-step anodization.

研究领域: 环境科学 · 材料科学
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Journal of Physical Chemistry C · 2024 · IF 3.3

Highly Efficient Photocatalytic Conversion of Gas-Phase CO2 Using Bimetallic Porphyrin-Sensitized TiO2 Nanotube Arrays

Tongxin Xiao,Xige Wu,Hongbao Liang,Kangyue Qiao,Ying Chen

Solar-powered photocatalytic conversion of CO2 into green solar fuels is one of the effective ways to solve the global energy crisis and the greenhouse effect. A new artificial photosynthesis system composed of TiO2 nanotube arrays (TiO2NTs) and bimetallic porphyrin was fabricated, and their photocatalytic activities were evaluated by the reduction of gas-phase CO2 to CH4 under simulated solar irradiation. Compared to pure TiO2NTs and CoTCPP/TiO2NTs, bimetallic porphyrin-sensitized TiO2NTs displayed greatly ameliorated photocatalytic activity. Among them, Ni-CoTCPP/TiO2NTs exhibited the highest photoreduction efficiency, and the reduction rate of CO2 into CH4 was up to 52.27 μmol/cm2/h with the quantum efficiency of 1.002%, about 7 times higher than that of pure TiO2NTs. The increase in photocatalytic performance can be attributed to the enhancement of the light absorption capacity of Ni-CoTCPP/TiO2NTs and the higher charge separation efficiency. Furthermore, according to the results of the photocatalytic evaluation and photo(electro)chemical studies, a possible mechanism of CO2 photoreduction over Ni-CoTCPP/TiO2NTs was proposed.

研究领域: 材料科学 · 环境科学 · 能源科学
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ACS Sustainable Chemistry & Engineering · 2020 · IF 7.632

Black Phosphorus Quantum Dot-Sensitized TiO2 Nanotube Arrays with Enriched Oxygen Vacancies for Efficient Photoelectrochemical Water Splitting

Lingxia Zheng,Xiaoying Ye,Xiaolei Deng,Yongzhi Wang,Yijian Zhao,Xiaowei Shi,Huajun Zheng

Photon absorption, charge separation and transportation, and charge-induced reactions at the active sites are the main crucial factors involved in the photoelectrochemical (PEC) water splitting. Herein, a combination of black phosphorus quantum dot (BPQD) sensitization and defect engineering strategies is employed to optimize the PEC performance of one-dimensional TiO2 nanotube array (NTA) photoanodes. The as-prepared TiO2–x/BP electrode exhibits a strong photocurrent density under simulated solar light irradiation, which is almost ∼3 times higher than that of bare TiO2. Specifically, the photocurrent increment of TiO2–x/BP is even larger than the sum of TiO2–x and TiO2/BP, verifying the synergistic effect of oxygen vacancies and BPQD sensitization. The maximum photoconversion efficiency of TiO2–x/BP is as high as 0.35%, while the value of TiO2 NTAs is calculated to be 0.13%. The results reveal that oxygen vacancies and BPQDs in the TiO2–x/BP composite not only facilitate the charge separation and transportation but also enhance the activity and quantity of reactive sites for water oxidation. The present strategy might open new routes to develop high-performance photoelectrodes for water splitting.

研究领域: 材料科学 · 能源科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2020 · IF 16.683

Interpreting the enhanced photoactivities of 0D/1D heterojunctions of CdS quantum dots /TiO2 nanotube arrays using femtosecond transient absorption spectroscopy

Zhiping Yan,Wenchao Wang,Lili Du,Jixin Zhu,David Lee Phillips,Jingsan Xu

Heterojunctions of CdS quantum dots (QDs)/TiO 2 nanotube arrays (NTAs) were synthesized via a simple vapor transport approach. The 0D/1D QDs/NTAs electrodes exhibited 5-fold improvement efficiency for photocatalytic dye degradation and hydrogen evolution compared to pure TiO 2 NTAs in a photoelectrochemistry cell, which was attributed to the faster transportation and retarded recombination of electron-hole pairs in the 0D/1D heterostructures. Femtosecond transient absorption offers deep insights into the dynamics of the charge carriers, showing that surface-trapped electrons were generated within 1.2 ps. The lifetimes for recombination of electrons at shallow trap sites with holes and deep trapped electrons with holes are prolonged to 73.2 ps and 622.6 ps, respectively. The reduced charge transfer resistance is verified by electrochemical impedance spectroscopy. Mott-Schottky plots indicated downward shifts for both the conduction band and valence band in the heterostructure. Finally, a Z-scheme photoreactive mechanism is proposed to explain the enhanced catalytic activities.

研究领域: 材料科学 · 光化学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2016 ·Vol. 28 ·期 3 ·2867-2876 · IF 1.798

The influence of linker molecule on photovoltaic performance of CdS quantum dots sensitized translucent TiO2 nanotube solar cells

Yu Libo,Li Zhen,Song Hai

Based on translucent TiO 2 nanotube (NT) film, CdS quantum dots (QDs) were anchored onto TiO 2 NT film using different linker molecules including thioglycolic acid (TGA), mercaptopropionic acid (MPA) and cysteine via hydrothermal method. The CdS QDs sensitized TiO 2 NT (CdS/TiO 2 NT) electrodes were constructed to quantum dots-sensitized solar cells (QDSSCs). The photovoltaic performance analysis results of the QDSSCs show that the linker molecule plays a significant role in the solar cell performance. The QDSSC using cysteine as linker molecule exhibits best power conversion efficiency than the other QDSSCs using TGA or MPA as linker molecules. The incident photon-to-current conversion efficiency (IPCE) and the electrochemical impedance spectroscopy (EIS) analysis results indicate that amino group of cysteine may has two aspects of the role to improve the power conversion efficiency of the QDSSC, one is that the good charge transfer properties of the cysteine might depend on the good donor–acceptor abilities of the free electron pair of the amino group, another is that distance between the TiO 2 NT and the CdS QDs could be slightly decreased due to the cysteine could anchor the CdS QDs via both amino and thiol group.

研究领域: 材料科学 · 能源科学
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Analytical Methods · 2021 ·Vol. 13 ·期 15 ·1803-1809 · IF 2.896

TiO2 nanotube arrays decorated with BiOBr nanosheets by the SILAR method for photoelectrochemical sensing of H2O2

Mingqing Li,Li Li,Boya Li,Liying Zhai,Baohui Wang

The design and construction of a photoelectrochemical (PEC) sensor with excellent photoelectric properties and good photoelectrocatalysis activity is significant for the effective detection of analytes. In this paper, based on a two-step anodic oxidation method and successive ionic layer adsorption (SILAR) method, a TiO2 nanotube array (TNT) photoelectrochemical sensor modified with BiOBr nanosheets was constructed and applied for the detection of H2O2 for the first time. The photocurrent of the photoelectrochemical sensor increases with the increase of the H2O2 concentration under the irradiation of an 8 W UV lamp. Excellent linearity was obtained in the concentration range from 10 nM to 100 μM with a low detection limit of 5 nM (S/N = 3). This excellent photoelectrochemical performance is due to the formation of a p–n heterojunction between BiOBr and TiO2 nanotube arrays, which provides efficient separation of charge carriers and accelerates electron transport. Moreover, it is applied to detect H2O2 in milk samples and it showed a good recovery result ranging from 95.73% to 105.65%, which provides a promising new strategy for the detection of H2O2.

研究领域: 材料科学 · 分析化学
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ANALYST · 2018 ·Vol. 143 ·期 20 ·5030-5037 · IF 3.864

A ratiometric photoelectrochemical immunosensor based on g-C3N4@TiO2 NTs amplified by signal antibodies–Co3O4 nanoparticle conjugates

Qiong Wu,Fengxia Zhang,Huijuan Li,Zhihua Li,Qi Kang,Dazhong Shen

Herein, we report a ratiometric photoelectrochemical (PEC) immunosensor coupled with secondary antibodies–Co3O4 nanoparticle conjugates (Ab2–Co3O4 NPs) for signal amplification. The Ab1-g-C3N4@TiO2 NTs and BSA-g-C3N4@TiO2 NTs act as the sensing and reference photoelectrodes, where Ab1, BSA and TiO2 NTs are the capture antibodies, bovine serum albumin and TiO2 nanotube arrays, respectively. In the presence of target Ag, the sensing PEC photocurrent decreases due to the steric hindrance of Ab1 molecules, which increases the inner resistance of the photoelectrode. The signal-off response is enhanced further using Ab2–Co3O4 NP conjugates due to their steric hindrance effect and the consumption of electron donors by the Co3O4 NPs. Furthermore, the performance of the ratiometric PEC platform is tested using alpha-fetoprotein (AFP) as a model antigen. Under the optimal conditions, the concentration of AFP is detected in the range of 0.4 pg mL−1 to 40 ng mL−1 with a detection limit of 0.2 pg mL−1. This ratiometric strategy is beneficial to improve the reliability and anti-interference ability of PEC immunosensors.

研究领域: 生物医学工程 · 分析化学
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SENSORS AND ACTUATORS B-CHEMICAL · 2014 · IF 3.84

Highly selective and sensitive glucose sensors based on organic electrochemical transistors using TiO2 nanotube arrays-based gate electrodes

Jianjun Liao,Shiwei Lin,Yue Yang,Kai Liu,Wencai Du

In organic electrochemical transistor (OECT) based glucose sensors Pt-based electrodes are usually used as the gate electrodes due to its excellent electrocatalytic activity. In this paper, a cheap and biocompatible material, TiO 2 nanotube arrays (TNTAs), was used as the gate electrode of the OECT device for the first time. It is encouraging that the sensing performance of OECTs using TNTAs-based gate electrodes is comparable to or better than those of the previously reported OECTs using Pt-based gate electrodes. Highly sensitive and selective OECT devices can be obtained by modifying TNTAs electrodes with Pt nanoparticles (Pt-NPs) and enzyme (glucose oxidase). The device shows a linear response to the logarithm of glucose concentration over the range from 100   nM to 5   mM, and the detection limit as low as 100   nM was achieved, which is three orders of magnitude lower than that of a conventional electrochemical measurement with the same electrode. On the other hand, the glucose can be selectively detected in the presence of interferences, such as ascorbic acid and uric acid, when the gate electrode is modified with Nafion. Moreover, the device presents a good stability and reproducibility. By modifying with other specific enzymes and nanomaterials, it is expected that many other type of enzyme sensors with high sensitivity and selectivity could be realized.

研究领域: 生物医学工程 · 材料科学 · 分析化学
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APPLIED SURFACE SCIENCE · 2017 · IF 3.387

High efficient photocatalytic activity from nanostructuralized photonic crystal-like p-n coaxial hetero-junction film photocatalyst of Cu3SnS4/TiO2 nanotube arrays

Yan Li,Fang-Ting Liu,Yin Chang,Jian Wang,Cheng-Wei Wang

Structuring the materials in the form of photonic crystals is a new strategy for photocatalytic applications. Herein, a new concept of photonic crystal-induced p-n coaxial heterojunction film photocatalyst of Cu 3 SnS 4 /TiO 2 (CTS/PhC-TNAs) was well-designed and successfully fabricated by combining periodic pulse anodic oxidation and in-situ self-assembling methods Such nanostructured CTS/PhC-TNAs exhibited significantly improved photocatalytic degradation activity under simulated sunlight irradiation with methyl orange (MO) as the target pollutants. Within 120   min, 82% of the MO (10   mg/L) was photodegraded and its kinetic constant per specific surface area reached 0.05332   μmol/m 2 h, which is 1.6 and 12.8 times more quickly than that of PhC-TNAs and CTS, respectively. Its significantly enhanced photocatalytic activity could be mainly attributed to a joint effect of the unique photonic crystal property of PhC-TNAs and the nanostructured hollow p-n coaxial hetero-junction, which result in an increased efficiency of charge separation and transfer and also an improved spectral response capability. This photonic crystal film photocatalyst has the potential for enhancing the photocatalytic activity via further optimizing the photonic stop band of PhC-TNAs. The study presents a new means to design the kind of photonic crystal structural-induced novel photocatalysts with high photocatalytic activities in pollution treatment.

CAS / MDL: 68-12-2
研究领域: 材料科学 · 环境科学
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ELECTROCHIMICA ACTA · 2016 · IF 4.803

Mesoporous TiO2 and Co-doped TiO2 Nanotubes/Reduced Graphene Oxide Composites as Electrodes for Supercapacitors

Hong Xiao,Wenjun Guo,Bin Sun,Meishan Pei,Guowei Zhou

A series of mesoporous TiO 2 nanotubes/reduced graphene oxide (TiO 2 NT/RGO) and Co-doped TiO 2 NT/RGO composites were synthesized via a hydrothermal method. In this method, graphene oxide (GO) was reduced to RGO, whereas TiO 2 NT and Co-doped TiO 2 NT were prepared using poly(ethylene-glycol)-block-poly(propy glycol)-block-poly(ethylene-glycol) as a structure-directing agent through a simple solvothermal route. Their morphology and properties were determined using X-ray diffraction, field emission scanning electron microscopy, UV–vis diffuse reflectance spectra, and Raman measurement. Results indicated that TiO 2 NT displayed mesoporous structures with lengths ranging from about 3   μm to 10   μm, tube diameters ranging from about 400   nm to 600   nm, wall thickness of about 250   nm, and mesoporous walls of about 6   nm. The electrochemical performance of the TiO 2 -based electrodes for supercapacitor was confirmed by cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge–discharge in 0.5   mol   L −1 Na 2 SO 4 aqueous electrolyte solution. The Co-doped TiO 2 NT/RGO composite electrode with 10.00   wt.% GO exhibited a specific capacitance of 27.5   F   g −1 at a current density of 0.2   A   g −1 in a symmetrical two-electrode cell, whereas the specific capacitance of TiO 2 was 0.7   F   g −1 . The Co-doped TiO 2 NT/RGO composite electrode exhibited high rate capability and excellent long-term cycle stability. The outstanding performance of the Co-doped TiO 2 NT/RGO composite electrode was attributed to the synergistic effects on capacitive behavior of Co-doped TiO 2 NT combined with high electronic conductivity of the RGO sheets.

CAS / MDL: 123334-00-9
研究领域: 材料科学 · 电化学
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