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Nanoscale · 2013 ·Vol. 5 ·期 21 ·10573-10581 · IF 6.233

Self-doping and surface plasmon modification induced visible light photocatalysis of BiOCl

Jing Jiang,Lizhi Zhang,Hao Li,Weiwei He,Jun Jie Yin

In this study we demonstrate that self-doping and surface plasmon resonance could endow a wide-band-gap ternary semiconductor BiOCl with remarkable visible light driven photocatalytic activity on the degradation of organic pollutants and photocurrent generation properties. The self-doped BiOCl with plasmonic silver modification was synthesized by a facile one-pot nonaqueous approach and systematically characterized using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, UV-visible diffuse reflectance spectra, electron spin resonance, and X-ray photoelectron spectroscopy. The photocurrent enhancement was found to be intimately dependent on the irradiation wavelength and matched well with the intensity of the absorption of the Ag nanoparticles. Reactive species trapping experiments and electron spin resonance spectroscopy with 5,5-dimethyl-1-pyrroline-N-oxide spin-trapping adducts confirmed that more oxidative species could be generated from the photogenerated electrons due to the plasmon-excitation of the metallic Ag in the self-doped BiOCl with plasmonic silver modification, which is responsible for the great enhancement of photocatalytic activity and photocurrent. Surface photovoltage spectroscopy and time-resolved photoluminescence spectroscopy results revealed the transfer of plasmon-band-induced electrons from Ag nanoparticles into BiOCl and the acceleration effect of surface plasmon resonance-induced intense oscillating electric fields on this electron transfer. This study would not only provide direct evidence of plasmonic photocatalysis, but also shed light on the design of highly efficient metal–semiconductor composite photocatalysts.

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2017 ·Vol. 28 ·期 22 ·16696-16703 · IF 2.019

Synthesis of graphene oxide/Ag3PO4 composite with enhanced visible-light photocatalytic activity

Yan Qishe,Xie Xin,Lin Cuiping,Zhao Yalei,Wang Shenbo,Liu Yonggang

The nano-scale Ag 3 PO 4 was successfully synthesized by the silver ammonia complexing precipitation method at room temperature. And the Graphene oxide (GO)/Ag 3 PO 4 nanocomposites with different contents of GO were successfully synthesized using the electrostatic driving method. The as-prepared GO/Ag 3 PO 4 nanocomposites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and UV–visible diffuse reflectance spectroscopy (UV–Vis DRS), confirming that Ag 3 PO 4 were highly dispersed to GO sheet. The photocatalytic properties of GO/Ag 3 PO 4 were evaluated by the degradation of Methyl Orange (MO) under visible light irradiation and solar irradiation respectively. The results showed that the photocatalytic efficiencies of GO/Ag 3 PO 4 nanocomposites had enhanced largely and the kinetics reaction models were followed first-order. Furthermore, 5% GO/Ag 3 PO 4 exhibited the highest photocatalytic activity on degradation of MO under visible-light irradiation. The improved photocatalytic performances of the GO/Ag 3 PO 4 nanocomposites mainly attributed to the introducing of GO, which benefit for electron transfer and inhibit the recombination of electron–hole pairs, promoting the practical application of Ag 3 PO 4 in water purification.

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
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DALTON TRANSACTIONS · 2013 ·Vol. 43 ·期 3 ·982-989 · IF 3.806

Fullerene modified C3N4 composites with enhanced photocatalytic activity under visible light irradiation

Bo Chai,Xiang Liao,Fakun Song,Huan Zhou

Fullerene modified C3N4 (C60/C3N4) composites with efficient photocatalytic activity under visible light irradiation were fabricated by a simple adsorption approach. The as-prepared C60/C3N4 composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance absorption spectra (DRS), Fourier transform infrared spectroscopy (FTIR) and photoluminescence spectra (PL). The photocatalytic degradation of rhodamine B (RhB) by the C60/C3N4 composites was investigated and optimized, suggesting that the optimal amount of C60 in the composites was 1 wt%. The significantly enhanced photocatalytic activity could be attributed to the efficient separation of photogenerated electrons and holes in the C60/C3N4 composites. A possible mechanism of C60/C3N4 composites as photocatalysts was proposed.

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
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ACS Applied Materials & Interfaces · 2017 · IF 7.504

SiO2/TiO2 Nanocomposite Films on Polystyrene for Light-Induced Cell Detachment Application

Zhiguo Cheng,Kui Cheng,Wenjian Weng

Light-induced cell detachment shows much potential in in vitro cell culture and calls for high-performance light-responsive films. In this study, a smooth and dense SiO2/TiO2 nanocomposite thin film with thickness of around 250 nm was first fabricated on H2O2 treated polystyrene (PS) substrate via a low-temperature sol–gel method. It was observed that the film could well-adhere on the PS surface and the bonding strength became increasingly high with the increase of SiO2 content. The peeling strength and shear strength reached 3.05 and 30.02 MPa, respectively. It was observed the surface of the film could transform into superhydrophilic upon 20 min illumination of ultraviolet with a wavelength of 365 nm (UV365). In cell culture, cells, i.e., NIH3T3 and MC3T3-E1 cells, cultured on SiO2/TiO2 nanocomposite film were easily detached after 10 min of UV365 illumination; the detachment rates reached 90.8% and 88.6%, respectively. Correspondingly, continuous cell sheets with good viability were also easily obtained through the same way. The present work shows that SiO2/TiO2 nanocomposite thin film could be easily prepared on polymeric surface at low temperature. The corresponding film exhibits excellent biocompatibility, high bonding strength, and good light responses. It could be a good candidate for the surface of cell culture utensils with light-induced cell detachment property.

研究领域: 材料科学 · 生物医学工程 · 细胞生物学
✓ 已验证 DOI PubMed 高影响因子
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ACS Applied Materials & Interfaces · 2021 · IF 9.229

Photo-Responsive Fluorosurfactant Enabled by Plasmonic Nanoparticles for Light-Driven Droplet Manipulation

Guangyao Cheng,Kuan-Ting Lin,Yinghua Ye,Hang Jiang,To Ngai,Yi-Ping Ho

The past decade has witnessed a significant development of droplet microfluidics for applications such as directed evolution and single-cell analysis. While the stability and manipulation of droplets are part of the prerequisites to further their applications, most of the currently available surfactants serve solely as stabilizers between the interfaces of water and oil. In this study, we present a novel type of photo-responsive fluorosurfactant based on fluorinated plasmonic nanoparticles (NPs). The demonstration by fluorinated gold–silica core–shell NPs (f-Au@SiO2) has been shown to be effective in stabilizing the water-in-fluorocarbon oil droplets. More importantly, the photothermal response enabled by the f-Au@SiO2 has been shown to be promising for the movement of droplets as well as the alteration of interfacial stability. The unique photo-responsiveness provided by the plasmonic NPs is expected to gear up the droplet microfluidics with an “active” surfactant for reconfigurable optical manipulation.

研究领域: 材料科学 · 化学工程 · 微流控技术
✓ 已验证 DOI PubMed 高影响因子
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CHEMICAL ENGINEERING SCIENCE · 2022 · IF 4.889

Kinetics of light assisted catalytic reduction of 4-NP over Ag/PDA

Kun Wang,Xun Zhu,Rong Chen,Dingding Ye,Yang Yang,Qiang Liao

In this work, Ag nanoparticles as surface plasmon catalysts were prepared on polydopamine microspheres via in-situ reduction for catalytic 4-nitrophenol to 4-aminophenol in the presence of sodium borohydride. The kinetics of catalytic reaction under light and dark conditions was compared. It was found that the reaction rate constant under light condition was increased by 53.6% due to the surface plasmon resonance effect. The transition state theory was used to reveal the enhanced mechanism of catalytic conversion of 4-nitrophenol under light condition. It is demonstrated that the light-excited high-energy electrons are responsible for the shift of the adsorbed reactants to the excited state with higher potential energy, lowering the apparent activation energy from 47.2 kJ/mol to 32.6 kJ/mol and thereby enhancing the conversion of 4-nitrophenol to 4-aminophenol. This study offers a deep insight into the contribution of surface plasmon resonance to catalytic conversion of 4-nitrophenol by surface plasmon catalysts.

研究领域: 化学 · 材料科学 · 光催化
✓ 已验证 DOI 高影响因子
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TALANTA · 2021 · IF 6.057

Enzyme-instructed self-assembly enabled fluorescence light-up for alkaline phosphatase detection

Yiming Zhang,Yinghao Ding,Xinxin Li,Zhenghao Zhang,Xiangyang Zhang,Yumiao Chen,Zhimou Yang,Yang Shi,Zhi-Wen Hu

Alkaline phosphatase (ALP) exists in both normal and pathological tissues. Spatiotemporal variations in ALP levels can reveal its potential physiological functions and changes that occur during pathological conditions. However, it is still challenging to exploit fluorescent probes that can measure ALP activity under good spatial and temporal resolutions. Herein, enzyme-instructed self-assembly (EISA) was used to construct a high-performing analytical tool (MN-pY) to probe ALP activity. MN-pY alone (free state) showed negligible fluorescence but presented an almost 13-fold increase in fluorescence intensity in the presence of ALP (assembly state). Mechanism study indicated the increase in fluorescence intensity was due to hydrogelation and formation of supramolecular fibrils, mainly consisting of dephosphorylated MN-Y. The dephosphorylation and further fibrillation of MN-pY could induce the formation of a “hydrophobic pocket”, leading to a further increase in fluorescence intensity. Moreover, MN-pY could selectively illuminate HeLa cells with a higher ALP expression but not LO2 cells with lower ALP levels, promising a potential application in cancer diagnosis.

研究领域: 生物化学 · 医学诊断 · 材料科学
✓ 已验证 DOI PubMed 高影响因子
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Nanoscale Advances · 2021 ·Vol. 3 ·期 8 ·2325-2333 · IF 4.553

Near-infrared light excited photodynamic anticancer therapy based on UCNP@AIEgen nanocomposite

Shihui Ding,Wenbo Wu,Tingting Peng,Wen Pang,Pengfei Jiang,Qiuqiang Zhan,Shuhong Qi,Xunbin Wei,Bobo Gu,Bin Liu

Photodynamic therapy (PDT), a clinically approved cancer treatment strategy, features non-invasiveness, few side-effects, high spatial resolution, etc. The advancement of PDT has been significantly restricted by the penetration depth of the excitation light. Herein, an effective fluorogen, TBD, with aggregation-induced emission characteristics (AIEgen) and high reactive-oxygen-species (ROS) generation efficiency was reported and integrated with a near infrared (NIR) light excitable upconversion nanoparticle (UCNP) to construct NIR light excitable UCNP@TBD nanocomposites. The formed nanocomposite has excellent photostability, good biocompatibility, and efficient ROS generation under NIR light excitation via Förster resonance energy transfer (FRET), enabling NIR light excited PDT. Moreover, the proposed NIR light excited PDT can break the impasse between the penetration depth and excitation volume in conventional PDT, effectively improving the anticancer therapeutic outcome. In vitro cancer cell ablation and in vivo tumor growth inhibition validated that the proposed UCNP@TBD nanocomposite is a promising NIR light excitable PDT agent with great potential for future translational research.

研究领域: 生物医学工程 · 肿瘤学 · 纳米医学
✓ 已验证 DOI PubMed 高影响因子
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Frontiers in Bioengineering and Biotechnology · 2022 · IF 6.064

Thermo- and Light-Responsive Polymer-Coated Magnetic Nanoparticles as Potential Drug Carriers

Cui Guihua,Wang Hao,Long Shengsen,Zhang Tianshuo,Guo Xiaoyu,Chen Shuiying,Kakuchi Toyoji,Duan Qian,Zhao Donghai

A series of thermo- and light-responsive copolymers of poly (N-isopropylacrylamide) (PNIPAM) and 6-[4-(4-methoxy phenyl azo)-phenoxyl-hexyl methacrylate) (AzoMA) (PNIPAM-b-PAzoMA) were synthesized via reversible addition–fragmentation chain transfer (RAFT) radical polymerization. The resulting copolymers had a narrow molecular weight distribution range of 1.06–1.24, in which Mn changed regularly with the monomer concentration. Subsequently, the diblock copolymers were successfully modified on the surface of iron oxide nanoparticles through the interaction between the chemical bonds to prepare Fe3O4@(PNIPAM-b-PAzoMA) nanoparticles. The size of fabricated nanoparticles with excellent thermo-sensitivity and photo-sensitivity was controlled at about 40–50 nm. Cell viability assays suggested that the nanoparticles showed no significant cytotoxicity and potential drug delivery in the tumor microenvironment.

研究领域: 材料科学 · 生物医学工程 · 药学
✓ 已验证 DOI PubMed 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Enhanced visible light-excited ZnSnO3 for room temperature ppm-level CO2 detection

Kewei Liu,Zichen Zheng,Jinyong Xu,Chao Zhang

Aimed at the bottleneck problem in conventional gas sensors that the effective detection of CO 2 gas can only be accomplished at concentrations above thousands of ppm and higher operating temperature, in this work, microstructured ZnSnO 3 equipped with rambutan-like hexahedral features with the hollow interior was successfully synthesized through a facile one-step hydrothermal method. Visible light was utilized as an excitation source to further enhance the sensing property. The investigation elaborated that at optimum hydrothermal time of 16 h, ZnSnO 3 showed a high gas response (~4.65), repeatability, and long-term stability towards 400 ppm CO 2 at room temperature. The response under purple light was 3.5 times higher than that under dark conditions, resulting from photoelectrons' generation. Furthermore, ZnSnO 3 sensor had excellent selectivity to 50 ppm CO 2 . The large specific surface area and abundant oxygen vacancies of ZnSnO 3 contribute to the excellent gas-sensing performance, which addresses the dilemma that it is difficult to break through the energy barrier through surface interaction to impact the band structure and carrier concentration because CO 2 is a non-polar molecule formed by polar bonds. Therefore, ZnSnO 3 is a promising material for the development of devices utilized in medical respiratory detection, agricultural crop growth detection and other fields.

研究领域: 材料科学 · 环境科学
✓ 已验证 DOI 高影响因子
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INORGANIC CHEMISTRY · 2020 · IF 4.825

One-Dimensional Face-Shared Perovskites with Broad-Band Bluish White-Light Emissions

Wei-Feng Zhang,Wen-Jing Pan,Te Xu,Ru-Yang Song,Yan-Yu Zhao,Cheng-Yang Yue,Xiao-Wu Lei

In recent years, two-dimensional (2D) hybrid lead halide perovskites based on corner-shared [PbX6] octahedrons have received extensive attention with important potentials in single-component white-light emitting diodes (WLEDs) due to the soft and distorted crystal lattices. However, limited research focused on the one-dimensional (1D) perovskites although they possess similar structural superiorities to achieve this performance. Herein, by using different types of organic amine cations as structural direction reagents, we report one new type of hybrid 1D perovskites of APbCl3 (A = (DTHPE)0.5, DMTHP, DBN) based on the same 1D face-shared octahedral [PbCl3]− chains. Upon UV light excitation, these 1D APbCl3 perovskites exhibit intrinsic broad-band bluish white-light emissions covering entire visible light spectra with the highest photoluminescence quantum yield (PLQY) of 6.99%, which catches up with the values of previously reported 2D perovskites. Through the systematical studies of time-resolved, temperature-dependent PL emissions, theoretical calculations, and so on, these broad-band light emissions can be ascribed to the radiative transition within conjugated organic cations. The facile assembly process, intrinsic broad-band light emissions, and high PLQYs enable these 1D APbCl3 perovskites as new types of promising candidates in fabricating single-component WLEDs.

研究领域: 材料科学 · 光学
✓ 已验证 DOI PubMed 高影响因子
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LANGMUIR · 2018 · IF 3.789

Surface with Reversible Green-Light-Switched Wettability by Donor–Acceptor Stenhouse Adducts

Haiquan Zhao,Dongsheng Wang,Yue Fan,Mingrui Ren,Shumin Dong,Yonghao Zheng

In this report, we designed surfaces with reversible green-light-switched wettability via donor–acceptor Stenhouse adducts (DASAs). Photoresponsive micro/nanoparticles were prepared by coating the surfaces of silica micro/nanoparticles with polydopamine and then postmodifying with DASA molecules. Then, the particles were immobilized on a glass substrate surfaces either with double-sided adhesive tape or cross-linking poly(dimethylsiloxane). Silica micro/nanoparticles with various diameters (0.2, 2.5, and 85 μm) were used to fabricate the photoresponsive surface. Green light irradiation switches the hydrophobic linear DASA to a hydrophilic cyclic isomer, which further increases the wettability and contact angle hysteresis on the surface. On the other hand, heating (100 °C) induces the cyclic-to-linear isomerization of DASA molecules and switches the surface back to hydrophobic. The wettability of the DASA-modified surface is reversible under alternate green light irradiation and heating.

研究领域: 材料科学 · 表面化学
✓ 已验证 DOI PubMed 高影响因子
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