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TALANTA · 2018 · IF 4.244

Two-dimensional TiO2 nanoflakes enable rapid SALDI-TOF-MS detection of toxic small molecules (dyes and their metabolites) in complex environments

Chan Gao,Deshuai Zhen,Ni He,Zhengbin An,Qiulan Zhou,Chenyi Li,Craig A. Grimes,Qingyun Cai

High surface area (136 m 2 g −1 ) nanoporous two-dimensional TiO 2 nanoflakes are applied as an adsorbent and meanwhile a matrix for toxic small molecule analysis using positive-ion surface-assisted laser desorption/ionization time-of-flight mass spectrometry (SALDI-TOF MS). The TiO 2 nanoflakes enable one-step enrichment and analysis, greatly simplifying the analysis technique. Due to the high enrichment efficiency and low background noise, small molecule organic contaminants at ppt or even sub-ppt concentrations such as malachite green (10 pg/mL), leucomalachite green (10 pg/mL), cetyltrimethylammonium bromide (0.001 pg/mL), rhodamine B (0.001 pg/mL), and crystal violet (0.1 pg/mL) were detected. In addition, malachite green and its metabolite leucomalachite green at ng/mL concentrations were successfully detected from fish blood and fish extracts, and crystal violet and its homologues at ng/cm 2 concentrations were detected from inks on thermal receipt papers obtained from local supermarket.

研究领域: 分析化学 · 环境科学 · 毒理学
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Journal of Materials Chemistry A · 2015 ·Vol. 3 ·期 12 ·6455-6463 · IF 7.443

In situ synthesis of mesoporous single-grain layer anatase TiO2 nanosheets without additives via a mild and simple process for a long-term Li-ion battery

Kunlei Zhu,Xiaoyan Liu,Jiangyong Du,Jianhua Tian,Yun Wang,Shengzhong Liu,Zhongqiang Shan

There are few reports on mesoporous anatase TiO2 nanosheets being synthesized without additives and ex situ templates under mild conditions. In this study, mesoporous single-grain layer anatase (MSGLA) TiO2 nanosheets were first synthesized in situ without additives in a new methanol–tetrabutyl titanate (TBT) system on a large scale using a simple and easily reproducible method. The formation mechanism of the MSGLA TiO2 nanosheets was investigated in detail. The results suggest that MSGLA TiO2 nanosheets can be obtained after a simple thermal treatment of amorphous TiO2 sheets that are converted in situ from the precursor Ti(OC4H9)4−n(OCH3)n (1 ≤ n ≤ 4) (TBM), which is gained easily via the transesterification reactions of TBT and anhydrous methanol at room temperature. Moreover, the MSGLA TiO2 nanosheets were applied successfully as anode materials for Li-ion batteries (LIB) and exhibited a discharge capacity of ∼73 mA h g−1 with obvious voltage plateaus over 4000 cycles (a test time of ∼50 days) at 5 C (1 C = 170 mA g−1) and Coulombic efficiencies of each cycle approaching 100%, highlighting them as promising materials for long-term LIB.

CAS / MDL: 13463-67-7
研究领域: 材料科学 · 纳米技术 · 能源存储
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ACS Applied Materials & Interfaces · 2023 · IF 9.5

Synergy of Surface Phosphates and Oxygen Vacancies Enables Efficient Photocatalytic Methane Conversion at Room Temperature

Xin-Ke Zhou,Yu Li,Pei-Pei Luo,Tong-Bu Lu

Room-temperature photocatalytic conversion of CH4 into liquid oxygenates with O2/H2O provides an appealing route for sustainable chemical industry, which, however, suffers from poor efficiency due to the undesired carrier kinetics and low yield of reactive oxygen species of the currently available photocatalysts. Here, we report an effective surface engineering strategy where concurrent constructions of oxygen vacancies and phosphate sites on TiO2 nanosheets address the above challenge. The surface oxygen vacancies and phosphates are respective acceptors of photogenerated electrons and holes for promoted separation and migration of charge carriers. Moreover, in addition to the facilitated activation of O2 to •OH by electrons at oxygen vacancies, the surface phosphates also facilely adsorb H2O via hydrogen bonds and thus effectively transfer holes to H2O for enhanced •OH production, thereby boosting CH4 conversion. As a result, compared with TiO2 sheets with only oxygen vacancies, a 2.8 times improvement in liquid oxygenate production with near-unity selectivity is achieved by virtue of the synergy of surface oxygen vacancies and phosphate sites, together with an unprecedent quantum efficiency of 19.8% under 365 nm irradiation.

CAS / MDL: 631-61-8 5593-70-4
研究领域: 化学工程 · 材料科学 · 环境科学 · 催化
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NEW JOURNAL OF CHEMISTRY · 2019 ·Vol. 43 ·期 22 ·8551-8556 · IF 3.069

Combined photoanodes of TiO2 nanoparticles and {001}-faceted TiO2 nanosheets for quantum dot-sensitized solar cells

Qiqian Gao,Xiaojuan Sun,Xijia Yang,Liying Wang,Xuesong Li,Xueyu Zhang,Lianfeng Duan,Wei Lü

A key point for constructing quantum dot-sensitized solar cells (QDSSCs) with high efficiency is to improve the utilization of sunlight. While various TiO2 morphologies such as nanoparticles, nanosheets, nanotubes and nanorods have been used as photoanodes of QDSSCs for improving cell performance, these investigations are generally focused on a single morphology of TiO2. Herein, a combined photoanode structure based on TiO2 nanoparticles and {001}-faceted TiO2 nanosheets have been designed, which exhibits improvement in cell performance. Owing to the strong light scattering and fast electron transfer ability of TiO2 nanosheets, an optimal power conversion efficiency of 4.98% with a short circuit current density (Jsc) of 17.57 mA cm−2, an open circuit voltage (Voc) of 0.63 V and a fill factor (FF) of 0.45 is achieved compared to the TiO2 nanoparticle photoanode (3.61%). The present work offers a feasible method towards improving the efficiency of QDSSCs.

研究领域: 材料科学 · 太阳能 · 纳米技术
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

S-scheme heterojunction Cu-porphyrin/TiO2 nanosheets with highly efficient photocatalytic reduction of CO2 in ambient air

Feng Yue,Mengke Shi,Cong Li,Yang Meng,Shuo Zhang,Lan Wang,Yali Song,Jun Li,Hongzhong Zhang

Directly capturing CO 2 in ambient air and converting it into value-added fuels using photocatalysis is a potentially valuable technology. In this study, Cu-porphyrin (tetrakis-carboxyphenyl porphyrin copper, CuTCPP) was innovatively anchored on the surface of TiO 2 (titanium dioxide) nanosheets to form an S-scheme heterojunction. Based on this, a photocatalytic reaction system for stably converting CO 2 in ambient air into value-added fuels at the gas–solid interface was constructed without addition of sacrificial agents and alkaline liquids. Under the illumination of visible light and sunlight, the evolution rate of CO is 56 μmol·g −1 ·h −1 and 73 μmol·g −1 ·h −1 , respectively, with a potential CO 2 conversion rate of 35.8 % and 50.4 %. The enhanced of photocatalytic performance is attributed to the introduction of CuTCPP, which provides additional active sites, significantly improves capture capacity of CO 2 and the utilization of electrons. Additionally, the formation of S-scheme heterojunction expands the redox range and improves the separation efficiency of photo-generated charges.

CAS / MDL: 1317-70-0 5593-70-4
研究领域: 光催化 · 材料科学 · 环境科学 · 化学
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Polydopamine-based surface coating fabrication on titanium implant by combining a photothermal agent and TiO2 nanosheets for efficient photothermal antibacterial therapy and promoted osteogenic activity

Gang Yang,Rongrong Deng,Yincheng Chang,Hongbo Li

Developing titanium-based dental implants with both excellent antibacterial properties and good osseointegration is crucial for the success of the implant operation and the long-term durability of the implant. In this study, a polydopamine-based coating was created by attaching TiO 2 nanosheets-cyanine composites onto the titanium surface, enabling the integration of effective photothermal antibacterial therapy with osseointegration. The exceptional dual-photothermal conversion abilities of polydopamine and cyanine in the coating resulted in outstanding photothermal antibacterial and antibiofilm therapy against four types of bacteria. Furthermore, TiO 2 nanosheets promoted the adhesion, proliferation and early osteogenic differentiation of osteoblasts. In an infected dental implant model in rats, the developed coating exhibited potent antibacterial activity and remarkable osteogenic differentiation in the bone, leading to increased bone formation around the implants. This innovative approach, combining photothermal therapy with osteogenic two-dimensional nanomaterials, presents a novel method for surface functionalization of implants to achieve effective antibacterial and osseointegration capabilities.

研究领域: 生物材料 · 牙科种植学 · 光热疗法 · 组织工程 · 生物医学工程
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ELECTROCHEMISTRY COMMUNICATIONS · 2024 · IF 4.7

Electrodeposited graphene@TiO2 nanosheets for enhanced photocathodic protection

Qian-Yu Wang,Teng Xu,Ji-Ming Hu

In this work, TiO 2 was firmly attached on freestanding graphene (Gr, rather than graphene oxide or reduced graphene oxide) nanosheets (Gr@e-TiO 2 ) by a novel electrodeposition method. The morphology, crystal structure, band gap characteristics, optical properties and photoelectric properties were systematically investigated. It is indicated that the absorption of visible light increased and the recombination of photogenerated electron-hole pairs decreased for the as-obtained Gr@e-TiO 2 . Compared with pure TiO 2 as well as GO (graphene oxide)@h-TiO 2 prepared by conventional hydrothermal method, Gr@e-TiO 2 exhibited a more negative open circuit potential and higher photocurrent density for 304SS protection. The enhanced photocathodic protection performance of Gr@e-TiO 2 can be attributed to the large specific surface area and good charge transport efficiency of graphene.

CAS / MDL: 7722-84-1 123334-00-9
研究领域: 材料科学 · 电化学 · 纳米技术 · 腐蚀防护
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Nano Research · 2023 ·Vol. 17 ·期 3 ·1173-1181 · IF 9.9

Flexo-photocatalysis in centrosymmetric semiconductors

Liu Kang,Wu Tong,Xu Luying,Zhang Zhuangzhuang,Liu Zhiyu,Wang Longfei,Wang Zhong Lin

The separation of photogenerated electron–hole pairs is vitally important for photocatalysis, which can be effectively promoted by polarization field. However, it only manifests in piezoelectric/pyroelectric/ferroelectric materials that have a non-centrosymmetric structure. Here, we demonstrate that the polarization enhanced photocatalysis (with wide spectra from ultraviolet (UV) light to visible light) can be achieved in centrosymmetric semiconductors, such as δ-MnO 2 and TiO 2 nanosheets integrated nanoflowers, by using the strain-gradient-induced flexoelectric polarization that is always overlooked in polarization-enhanced catalysis. Under ultrasonic and illumination excitation, the organic pollutants (methylene blue (MB), etc.) can be effectively degraded within 30 min with excellent stability and repeatability. Compared with photocatalysis, the flexo-photocatalytic performance of above centrosymmetric semiconductors is substantially increased by 85%. Moreover, the factors related to flexo-photocatalysis such as material morphology, mechanical stimuli source, and adsorption are explored to deeply understand the mechanism of flexo-photocatalysis. This work opens up a way for high-performance photocatalysis in centrosymmetric semiconductors.

研究领域: 光催化 · 材料科学 · 半导体物理 · 纳米技术 · 环境科学
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ChemSusChem · 2016 ·Vol. 9 ·期 10 ·1118-1124 · IF 7.116

Fabrication of 3 D Mesoporous Black TiO2/MoS2/TiO2 Nanosheets for Visible-Light-Driven Photocatalysis

Xuefeng Liu,Zipeng Xing,Hang Zhang,Wenmei Wang,Yan Zhang,Zhenzi Li,Xiaoyan Wu,Xiujuan Yu,Wei Zhou

Graphical Pass the Mo : A 3 D sandwich of mesoporous black TiO 2 (MBT)/MoS 2 /MBT was fabricated using a facile mechanochemistry method combined with an in situ solid-state chemical reduction approach. The material exhibited excellent visible-light-driven photocatalytic performance for pollutant degradation and hydrogen evolution owing to the sandwich-like heterojunction structure and Ti 3+ doping. A novel 3 D mesoporous black TiO 2 (MBT)/MoS 2 /MBT sandwich-like nanosheet was successfully fabricated using a facile mechanochemical process combined with an in situ solid-state chemical reduction approach, followed by mild calcination (350 °C) under an argon atmosphere. The MBT/MoS 2 /MBT exhibits a 3 D sandwich-like nanosheet structure and heterojunctions are formed at the interfaces between MoS 2 and black TiO 2 . The significantly narrowed band gap of MBT/MoS 2 /MBT is attributed to the introduction of MoS 2 and the formed Ti 3+ species in the frameworks. The visible-light photocatalytic degradation rate of methyl orange and the hydrogen production rate are as high as 89.86 % and 0.56 mmol h −1 g −1 , respectively. The introduction of MoS 2 and Ti 3+ in the frameworks favors the visible-light absorption and the separation of photogenerated charges, and the 3 D sandwich-like heterojunction structure facilitates the transfer of photogenerated charges.

CAS / MDL: 16940-66-2
研究领域: 材料科学 · 化学 · 环境科学 · 能源科学
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2022 ·Vol. 414 ·期 5 ·1829-1839 · IF 4.478

Dual-mode detection of dopamine based on 0D/2D/2D CuInS2/ZnS quantum dot–black phosphorous nanosheet–TiO2 nanosheet nanocomposites

Yi Jinquan,Chen Xiaoping,Lin Jianwei,Song Kai,Han Zhizhong,Chen Jinghua

In this work, we designed new dual-mode “turn-on” electrochemical (EC) and photoelectrochemical (PEC) sensors for the detection of dopamine (DA) based on 0D/2D/2D CuInS 2 /ZnS quantum dot (QD)–black phosphorous nanosheet (BPNS)–TiO 2 nanosheet (TiO 2 NS) nanocomposites. QDs can not only improve the photocurrent of the developed PEC sensors, but also provide the electrochemical signal in the EC detection. BPNSs as p-type semiconductor with high conductive properties work as electron acceptors and are utilized to improve the sensitivity of the DA PEC and EC sensors. Under irradiation of visible light or the applied voltage, DA is both excited and releases electrons, realizing “turn-on” detection. The PEC sensors have a linear range of 0.1–100 μM with a lower detection limit of 0.028 μM. For the EC detection, BPNSs can accelerate electron transfer which attribute to its excellent conductivity. In the range of 1–200 μM, the working curve of DA detection by the EC sensors was established and the detection limit is 0.88 μM. Comparing the two methods, the PEC sensors have a lower detection limit, and the EC sensors have a wider monitoring range. The dual-mode sensors of EC and PEC pave an effective way for the detection in biological and medical fields. Graphical abstract

研究领域: 分析化学 · 材料科学 · 生物医学工程 · 纳米技术
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CERAMICS INTERNATIONAL · 2022 · IF 5.532

Efficient interfacial solar driven water evaporation and photocatalytic pollutant degradation by partially oxidized TiH1.924/TiO2 nanosheet

Ruizhi Xue,Ruirui Huang,Binbin Wu,Ning Li,Qing Chang,Chaorui Xue,Caihong Hao,Huiqi Wang,Jinlong Yang,Shengliang Hu

Interfacial solar driven water evaporation (ISDWE) and photocatalytic pollutant degradation (PPD) have been considered as efficient and green technologies for tackling the water crisis. Here, through hydrothermal treatment of TiH 1.924 /Ti powders, we designed a hybrid material composed of partially oxidized TiH 1.924 and TiO 2 nanosheets with outstanding ISDWE and PPD performances. Titanium suboxides can be formed inside the compound of partially oxidized TiH 1·924 /TiO 2 nanosheet, and induce efficient solar-thermal transformation. Meanwhile, TiO 2 nanosheet is conducive to reducing the water vaporization enthalpy, ensuring adequate water supply, and enlarging the surface area for evaporation. Due to the synergies between partially oxidized TiH 1.924 and TiO 2 nanosheet, the water evaporation rate achieved 1.70 kg m −2 •h −1 under solar radiation of 1.0 kW m −2 , which is higher than most reported titanium compounds. The investigation on the PPD performance showed that the photothermal effect and band alignment collaboratively improved the photodegradation of rhodamine B by partially oxidized TiH 1·924 /TiO 2 nanosheets. The excellent PPD property can promote the long-term ISDWE application of partially oxidized TiH 1·924 /TiO 2 nanosheets by avoiding the dye accumulation. This study may provide valuable information for developing advanced composites, ISDWE and PPD technologies.

研究领域: 环境科学 · 材料科学 · 纳米技术 · 水处理
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Small · 2024 · IF 13

Synergistic Electronic Interaction in PdCu Alloy/TiO2-NSs for Ambient Efficient Dehydrogenation of Formic Acid

Saima Ashraf,Yanyan Liu,Shuling Liu,Sehrish Mehdi,Huanhuan Zhang,Ruofan Shen,Xianji Guo,Xianli Wu,Jianchun Jiang,Yongfeng Wang,Baojun Li

Palladium-based catalysts are remarkable in endorsing hydrogen (H 2 ) generation through formic acid (HCOOH, FA) dehydrogenation under near-ambient conditions. Hydrogen energy efficiency depends on high-performance catalyst design. In this study, Pd-Cu nanoalloy catalysts with mutable atomic ratios are successfully fabricated on TiO 2 nanosheets (TiO 2 -NSs).The synergistic electronic interactions between Palladium (Pd) and copper (Cu) are revealed through a density of states (DOS) analysis of alloy supported over a mixed valence state of Ti linked to oxygen vacancies (Vo) in TiO 2 -NSs, Enhanced adsorption of target molecules reveals novel active sites for Formic acid dehydrogenation (FAD), with O─H bond cleavage via HCOO formate intermediate preceding C─H and C─O bond cleavage. Experimental and theoretical research demonstrates that the Pd-Cu/TiO 2 -NSs (3:7) catalyst d electron redistribution and d-band center shift lower the activation energy for O─H bond cleavage, exhibit superior H 2 production than pure Pd and Cu, increasing Pd electron density due to synergistic effects from reactive crystal facets, defects, and strong metal support interactions (SMSI), lowering the activation energy for HCOOH dissociation step, generating carbon dioxide (CO 2 ) and H 2 with a unprecedented high turnover frequency (TOF) of 6268 mol H2 .h −1 .molPd −1 at 303K with activation energy ( E a ) of 15 KJ mol −1 . This attempt models an efficient HCOOH-to-hydrogen catalyst.

CAS / MDL: 5593-70-4
研究领域: 催化 · 材料科学 · 化学工程 · 能源科学
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