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MICROCHIMICA ACTA · 2025 ·Vol. 192 ·期 7 ·1-12 · IF 5.3

A bifunctional UIO-66-NH2@ RhB-based fluorescence and colorimetric dual-mode ratiometric sensor and hydrogel-based smart phone–assisted naked eye detection of perfluorooctanesulfonate (PFOS)

Aham Emmanuel Chigozie,Ravikumar A.,Feng Weiwei,Arunjegan A.,Hu Zhang,Zhang Zhen,Zhao Hongjun

A bifunctional fluorescent and colorimetric sensor based on UiO-66-NH₂@RhB was developed for the highly sensitive detection of perfluorooctanesulfonate (PFOS), a persistent environmental pollutant. The sensing mechanism relies on the inner filter effect (IFE), where Rhodamine B (RhB) modulates the fluorescence of UiO-66-NH₂, enabling effective PFOS recognition. In the presence of PFOS, UiO-66-NH 2 @RhB exhibits dual emissions in blue fluorescence at 448 nm and red fluorescence at 565 nm at a single excitation wavelength. Upon the addition of increasing concentrations of PFOS, the blue fluorescence intensity increased and a small change was observed in the red fluorescence intensity. Besides, UiO-66-NH 2 @RhB solutions display an excellent colorimetric response for PFOS and produce an obvious color change from red to colorless. The method demonstrated high sensitivity, achieving linear detection ranges of 1–10 nM with detection limits of 0.84 nM (fluorescence) and 0.91 nM (colorimetry). Furthermore, the dual-sensing platform successfully detected PFOS in real water samples with satisfactory outcomes. Its integration with a portable smartphone further enables intelligent, real-time, on-site monitoring and is successfully applied to monitoring PFOS in environmental samples. This study not only broadens the application of MOFs but also provides valuable insights for designing multifunctional sensors for diverse analytical applications. Graphical abstract

研究领域: 环境科学 · 分析化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2017 · IF 9.446

Combination of ultrafast dye-sensitized-assisted electron transfer process and novel Z-scheme system: AgBr nanoparticles interspersed MoO3 nanobelts for enhancing photocatalytic performance of RhB

Bing Feng,Zhengying Wu,Jinsong Liu,Kongjun Zhu,Ziquan Li,Xin Jin,Yindi Hou,Qingyang Xi,Mengqi Cong,Pengcheng Liu,Qilin Gu

Inspired by the natural photosynthesis in green plants, artificial heterogeneous Z-scheme photocatalytic systems are widely used to settle environmental concerns and energy crises, and their excellent characteristics come from long-term stability, wide absorption range, high charge-separation efficiency, and strong redox ability. However, the contribution of the surface-adsorbed dyes antenna molecule is seldom considered in the process of Z-scheme photocatalysis. In this study, we construct AgBr quantum dots decorated MoO 3 nanobelts as a novel Z-scheme photocatalyst by an oriented diffusing and charge induced deposition. For the first time, we find the synergistic effect caused by the suitable energy band match among RhB dyes, AgBr nanoparticles, and MoO 3 nanobelts, leading to the ultrafast dye-sensitized-assisted electron transfer process. This is responsible for excellent photocatalytic activities of the achieved AgBr/MoO 3 monolithic catalyst for degrading RhB under visible light irradiation. Simultaneously, changing of the band gaps and detailed mechanism for high efficiency degradation is analyzed and explored by theoretical calculations and designing further experiments. It is proposed that ultrafast degradation of the RhB on the AgBr/MoO 3 nanocomposites is due to both the photocatalytic process and the dye sensitization; the superoxide radical O 2 − , which is produced by accumulated dye-sensitization-induced abundant electrons with powerful potential in the CB of AgBr accompanying by quick combination of electrons in the CB of MoO 3 with photogenerated holes in the VB of AgBr, is a dominant reactive species for the degradation of RhB under visible light irradiation.

研究领域: 环境科学 · 材料科学 · 光化学
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 34 ·15202-15214 · IF 2.7

New insights into sulfite activation by amorphous Fe1−xNixS for RhB removal: the synergistic effect of free radical and non-free radical pathway

Jinyuan Zhang,Ziqin Xing,Jianxin Liu,Yawen Wang,Xiaochao Zhang,Rui Li,Yunfang Wang,Caimei Fan

Advanced oxysulfur radical-based advanced oxidation processes (OSR-AOPs) usually use heterogeneous catalysts to activate sulfite to degrade organic pollutants in water. In this study, we report the mechanism of sulfite activation by amorphous Fe1−xNixS to degrade rhodamine B (RhB) in different pH ranges. Compared with FeS, Fe1−xNixS had a wide pH application range and high activity. For Fe1−xNixS, Ni-doping sped up electron transfer inside the catalyst and the reduced S2− promoted the Fe(III)/Fe(II) cycle, which together improved the sulfite activation by Fe1−xNixS. The results indicated a pH dependence of RhB degradation in the Fe1−xNixS/sulfite system. The free radical pathway of SO3˙−, SO5˙− and ˙OH generated in the process was dominant under acidic condition, whereas it was mainly a non-free radical pathway of electron transfer between the catalyst and the pollutant under alkaline conditions. Both free radical and non-free radical pathways existed in Fe1−xNixS/sulfite under neutral conditions. The results shed significant light on promoting sulfite-based AOPs to remove pollutants from water.

CAS / MDL: 10257-55-3 7720-78-7
研究领域: 环境科学 · 化学工程
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MATERIALS RESEARCH BULLETIN · 2019 · IF 3.355

Enhanced photocatalytic activity and mechanism of Ti3C2−OH/Bi2WO6:Yb3+, Tm3+ towards degradation of RhB under visible and near infrared light irradiation

Hongjun Fang,Yusong Pan,Minyuan Yin,Chengling Pan

It is an effective method to explore full spectrum responsive photocatalyst for improving their photocatalytic activity. Herein, Ti 3 C 2 −OH/Bi 2 WO 6 :Yb 3+ , Tm 3+ composites were successfully synthesized via a facile hydrothermal method. The resultant Ti 3 C 2 −OH/Bi 2 WO 6 :Yb 3+ , Tm 3+ composites accompanied 2D/2D heterojunction with grid-like porous structure present a significant enhancement of photoactivity towards degradation of RhB under visible and NIR light irradiation. Specifically, the 0.2-Y/T-TB2.8 composite exhibits the best photocatalytic activity for RhB removal, in which the RhB degradation efficiency was 99.8% (Vis-NIR, 30 min), 91% (Vis, 30 min), and 48% (NIR, 160 min). The excellent photocatalytic activity of the composite is attributed to the grid-like porous structure endowing it with an enhanced RhB adsorption, favorable charge separation resulting from the outstanding conductivity of the Ti 3 C 2 −OH, and up-conversion mechanism via energy level transition of Yb 3+ /Tm 3+ . In addition, the radical capture experiments verified that the hole (h + ) plays the important role for degradation of RhB.

研究领域: 材料科学 · 环境科学 · 光化学
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Journal of Environmental Chemical Engineering · 2024 · IF 7.4

Highly sensitive and selective L-lactate monitoring in complex matrices with a ratiometric fluorescent sensor RhB@Zn-MOF

Bo Jing,Xinke Xu,Jingze Wang,Changyan Sun,Wenjun Li,Zhidong Chang

L-lactate is an essential biomarker in clinical diagnostics and food quality assessment. This study introduces a novel ratiometric fluorescence sensor, RhB@Zn-MOF, which was specifically designed for the sensitive and selective detection of L-lactate. Through the strategic incorporation of Rhodamine B (RhB) into Zn-MOF, RhB@Zn-MOF was synthesized, exhibiting dual-emission properties and could effectively distinguish L-lactate in complex biological and food matrices such as milk and sweat based on the competitive absorption mechanism. Notably, the sensor achieves a low detection limit of 0.091 μM and demonstrates excellent stability and reproducibility in varied conditions. Furthermore, the integration of the sensor with smartphone technology enables rapid, real-time analysis, showcasing potential applications in sports medicine, clinical environments, and the food industry.

研究领域: 分析化学 · 生物技术 · 临床诊断 · 食品科学 · 材料科学
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POLYHEDRON · 2024 · IF 2.4

Germ must be found: The HNT@RhB@MOF-Tb polychromatic fluorescent nanoprobe is applied for the visual detection of 2,6-dipicolinic acid

Jian Gou,Luxin Xing,Yousong Hu,Lina Zhang,Yongxin Li,Ning Bi,Yuanyuan Huang,Jun Xu,Lei Jia

A polychromatic fluorescent nanoprobe based on natural halloysite nanotubes with fluorescent dyes and porous metal–organic frameworks co-loaded on the surface and inner wall of the nanotubes was constructed for the highly sensitive visual identification of the Bacillus anthracis biomarker 2,6-dichlorophenolic acid (DPA). The limit of detection for DPA was 11.27 nM, which is significantly lower than the spore-borne dose for anthrax infection (60 uM). The multi-color fluorescent probe showed potential for rapid, accurate, and highly selective detection of Bacillus anthracis markers in actual samples. Besides, a portable fluorescence detection platform was developed in combination with a smartphone color scanning APP to simplify the detection process and realize real-time semi-quantitative analysis.

研究领域: 纳米技术 · 生物技术 · 分析化学 · 微生物学
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ACS Applied Nano Materials · 2024 · IF 5.3

Heterojunctions Based on BiOBr Nanosheets Decorated on α-Bi2O3 for Photodegradation of Rhodamine B

Xia Cheng,Xinyan Xiao,Fei Wang,Ting Lu,Yu Zhang

Photocatalysis is extensively implemented in organic pollutant degradation, and the critical point is to develop outstanding and stable photocatalysts. Herein, the synthesis of coral reef-like α-Bi2O3/BiOBr heterostructure photocatalysts involves the in situ growth of BiOBr nanosheets onto α-Bi2O3, with the latter derived through calcination utilizing a bismuth-based metal–organic framework (CAU-17) as the precursor. Under simulated sunlight, the 20% α-Bi2O3/BiOBr heterojunction degraded nearly 97.7% of RhB in 60 min, while pure α-Bi2O3 and BiOBr nanosheets degraded only 7.8 and 65.3%, respectively. Furthermore, the 20% α-Bi2O3/BiOBr nanocomposite exhibited superior recycling stability, degrading 86.6% RhB after four cyclic experiments. This is attributed to the fact that the nanoscale α-Bi2O3 material obtained by calcination can retain the exoteric diffusion channels of CAU-17, making α-Bi2O3/BiOBr heterojunctions have an enormous specific surface area, providing more adsorption sites and promoting their photocatalytic capacity. Free radical capture tests and electron paramagnetic resonance measurements indicated that h+ and •O2– were the primary active substances during photodegradation. On the basis of that, a feasible photodegradation mechanism of type II α-Bi2O3/BiOBr heterojunctions was proposed. This study opens up the possibility of designing type II heterojunctions with MOFs as precursors for dye degradation.

CAS / MDL: 81-88-9
研究领域: 材料科学 · 环境科学
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Inorganics · 2022 ·Vol. 10 ·期 3 ·27 · IF 3.149

Synthesis of MOFs for RhB Adsorption from Wastewater

Qinhui Ren,Meng Nie,Lili Yang,Fuhua Wei,Bo Ding,Hongliang Chen,Zhengjun Liu,Zhao Liang

Fe-MOFs were prepared using a solvothermal method, and were characterized by scanning electron microscopy. We explored the application of Fe-MOFs as an adsorbing material for the removal of Rhodamine B (RhB) from aqueous solutions. The experimental data were simulated by dynamics and the results showed that the pseudo–second-order kinetics model was appropriate for analysis of RhB removal. We studied the adsorption capacity of MOF materials under different masses, concentrations, and pH conditions. When the pH was 6, the maximum adsorption capacity within 4 h was 135 mg/g. In summation, the removal of RhB from wastewater using MOFs is feasible, inexpensive, and effective. Hence, our findings indicate that MOFs have a broad application in the purification of wastewater.Keywords:metal-organic frameworks;organic dye;wastewater

研究领域: 环境科学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2023 · IF 6.2

Enhanced visible-light photocatalytic performance of black TiO2/SnO2 nanoparticles

Yufang Li,Yangchun Feng,Hang Bai,Jinsong Liu,Dayuan Hu,Jiyu Fan,Honglie Shen

In recent years, large and small industries have discharged a multitude of organic pollutants into the environment, causing environmental pollution. Titanium dioxide (TiO 2 ) materials is very important photocatalyst as a result of its outstanding applications to remove organic contaminants from the environment. Nonetheless, the low utilization rate of visible light of TiO 2 has limited its application. To begin with, Black TiO 2 is produced by the magnesium thermal reduction method to promote the absorption of visible light, Subsequently, The black TiO 2 /SnO 2 composites are synthesized by chemical synthesis method to form a hetero-junction to augment the photocatalytic activity. The morphology, chemical composition, phase structure and photocatalytic degradation of Rhodamine B (RhB) under visible light irradiation were investigated. The morphological properties demonstrated that a Ti 3+ self-doped disorder layer forms on the surface of TiO 2 nanophase, and black TiO 2 nanoparticles are well decorated with SnO 2 nanoparticles. After 90 min of visible light irradiation, RhB has a photocatalytic degradation efficiency of 96.62%, which is 1.597 times that of TiO 2 nanoparticles, and its cycle stability is well beyond our expectation. The ameliorated photocatalytic degradation performance of TiO 2 /SnO 2 composite is ascribed to the formation of a "type Ⅱ heterojunction", which not only reinforces the absorption of visible light of black TiO 2 /SnO 2 nanoparticles, but also heightens the separation and transfer efficiency of the photogenerated carriers.

研究领域: 环境科学 · 材料科学
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MATERIALS CHEMISTRY AND PHYSICS · 2019 · IF 2.781

Construction of g-C3N4/Eu(III) doped Bi24O31Cl10 heterojunction for the enhanced visible-light photocatalytic performance

Zhilin Li,Chongyue Jin,Chunmei Lv,Min Wang,Jin Kang,Shiyu Liu,Yuanhua Xie,Tong zhu

To further promote the visible-light photocatalytic efficiency of Bi 24 O 31 Cl 10 , g-C 3 N 4 /Eu(III) doped Bi 24 O 31 Cl 10 heterojunction composites (CN/Eu-BCO) were successfully synthesized via modified solution combustion and immersion-calcination method. The effects of Eu(III) dopants and g-C 3 N 4 coupling on the micro-structures and the photocatalytic efficiency of Bi 24 O 31 Cl 10 towards Rhodamine B (RhB) degradation were investigated in detail. The results displayed that Eu(III) doping and coupling with g-C 3 N 4 can largely promote the photocatalytic efficiency of Bi 24 O 31 Cl 10 . The photodegradation rate of RhB over 5CN/0.01Eu-BCO can reach to be 91.9% in 40 min, which was 8.46 folds of Bi 24 O 31 Cl 10 , 1.91 folds of 0.01Eu-BCO, and 1.72 folds of 5CN/BCO. The main radical species being responsible for RhB degradation were ● O 2 − and ● OH. Furthermore, 5CN/0.01Eu-BCO composite photocatalyst exhibited good reusability and stability.

CAS / MDL: 81-88-9
研究领域: 材料科学 · 环境科学
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CHINESE JOURNAL OF CATALYSIS · 2017 · IF 2.813

Effect of carrier and axial ligand on the photocatalytic activity of cobalt thioporphyrazine

Yi Liu,Xuanmu Zhou,Zhehui Zhang,Bingguang Zhang,Kejian Deng

The photocatalytic activity of cobalt octakis(butylthio) porphyrazine (CoPz(BuS) 8 ) was assessed through photodegradation of the dye rhodamine B (RhB) in water under irradiation with a Xe lamp and aerated conditions. The photocatalytic activity of CoPz(BuS) 8 loaded on Al 2 O 3 or SiO 2 @Fe 3 O 4 nanoparticles or coordinated with an axial azide ligand was also investigated. The results demonstrated that the photocatalytic activity of CoPz(BuS) 8 loaded on Al 2 O 3 was higher than that loaded on SiO 2 @Fe 3 O 4 . The kinetic curves of RhB degradation in aqueous solutions at different pH indicated the pseudo first-order kinetics of the reaction. The highest degradation rate for CoPz(BuS) 8 loaded Al 2 O 3 at pH = 4 after 160 min was 84.6%. However, the advantages of easier separation and recycling as well as the ability to terminate the reaction at any time for the CoPz(BuS) 8 loaded SiO 2 @Fe 3 O 4 cannot be ignored. When electron-rich NaN 3 was coordinated with CoPz(BuS) 8 as an axial ligand and loaded on Al 2 O 3 , the resulting catalyst produced more active oxygen species such as O 2 − and HO • to promote the quicker degradation of RhB than that by the other catalysts. For the N 3 -coordinated CoPz(BuS) 8 loaded on Al 2 O 3 , the reactions at pH = 4 and 7 distinctly deviated from first-order kinetics, and the degradation rate reached 77.6% after 80 min at pH = 4.

CAS / MDL: 10026-22-9
研究领域: 化学 · 环境科学 · 材料科学
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JOURNAL OF ALLOYS AND COMPOUNDS · 2024 · IF 5.8

Photocatalytic activity of (002) crystalline facets for novel Bi-sourced Bi-MOF nanoparticles enhanced degradation of rhodamine B and reduction of hexavalent chromium

Jingjing Wang,Zhiwei Liu,Liying Wang,Lu Li,Qian Liu,Zhiwei Liu,Zhenzhu Cao,Yongfeng Zhang,Lin Cheng,Jucai Yang

Type II heterojunction photocatalysts possessed excellent redox properties and had great potential for environmental remediation applications. In this paper, a novel Bi source of Bi-MOF was created by using NaBiO 3 . Additionally, KCl was incorporated to contest Bi-MOF for the Bi source, with the objective of generating floral BiOCl. Subsequently, heterostructures based on metal-organic skeletons (MOFs) were constructed with Bi-MOF and BiOCl, with the aim of exposing the (002) crystal faces of BiBDC. The modification of the (002) crystal surface was employed to create holes or generate more photogenerated electrons, resulting in efficient degradation of rhodamine B (RhB) and simultaneous reduction of hexavalent chromium. The heterogeneous structure demonstrated a degradation rate of 97 % for rhodamine B (RhB) after reaching adsorption equilibrium in 30 min of dark reaction and 10 min of visible light irradiation. Furthermore, the reduction rate of hexavalent chromium (Cr (VI)) was 95.5 % after reaching adsorption equilibrium in 30 min of dark reaction and 70 min of visible light irradiation . The results of the cycling experiments demonstrated that both 1:1 BBOC and 1:3 BBOC retained their structural integrity following four cycles. The active species trapping results indicated that the hole radicals (h + ) and electrons were responsible for the degradation of RhB and the reduction of hexavalent chromium, respectively. This study also revealed the degradation pathways and mechanisms of heterojunctions, providing new ideas for the preparation of photocatalysts for environmental remediation.

研究领域: 环境科学 · 材料科学
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