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Green Energy & Environment · 2026 · IF 14.6

Metal-free C(CN)3 cooperated with Co-Ti dual sites in bimetallic CoTi-MOF as a tandem photocatalyst for highly efficient C2H4 production

Lijun Xiong,Dandan Zhu,Chenglong Qiu,Weihong Zeng,Mingshi Xu,Shanshan Wang,Yong Yang

The photocatalytic reduction of carbon dioxide (CO 2 ) into high-value C 2+ hydrocarbons represents a sustainable pathway to alleviate energy shortages and reduce atmospheric CO 2 levels. In this study, a unique tandem photocatalyst (CoTi-CN), is constructed by integrating bimetallic CoTi-MOF with metal-free half-metallic C(CN) 3 . This composite demonstrates markedly enhanced activity and selectivity in the photocatalytic CO 2 reduction to ethylene (C 2 H 4 ), achieving a C 2 H 4 selectivity of 36.8% and a generation yield of 31.3 μmol g −1 over 5 h. Density functional theory (DFT) calculations combined with in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) analysis reveal that C(CN) 3 acts as an efficient CO 2 to CO converter, while CoTi-MOF favors the adsorption and C-C coupling of *CO intermediates. The spatially decoupled CO generation and C-C coupling processes lead to optimized intermediate coverage and reduced energy barriers, resulting in superior selectivity toward multi-carbon products. This work opens new horizons for the design of tandem photocatalysts that combine half-metallic catalysts with bimetallic MOFs, achieving a significant enhancement in the activity and selectivity of photocatalytic C 2 H 4 production.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Fabrication of direct Z-scheme Cu2O@V-CN (octa) heterojunction with exposed (1 1 1) lattice planes and nitrogen-rich vacancies for rapid sterilization

Lifang Sun,Wen Li,Chengcheng Ma,Gaojian Lv,Huimeng Feng,Yanan Pu,Tianxiang Sun,Shougang Chen

The Z-scheme heterojunction has demonstrated significant potential for promoting photogenerated carrier separation. However, the rational design of all-solid Z-scheme heterojunctions catalysts and the controversies about carrier transfer path of direct Z-scheme heterojunctions catalysts face various challenges. Herein, a novel heterojunction, Cu 2 O@V-CN (octa), was fabricated using V-CN (carbon nitride with nitrogen-rich vacancies) in-situ electrostatic self-wrapping Cu 2 O octahedra. Density functional theory (DFT) calculations revealed that the separation of carriers across the Cu 2 O@V-CN (octa) heterointerface was directly mapped to the Z-scheme mechanism compared to Cu 2 O/V-CN (sphere). This is because the Cu 2 O octahedra expose more highly active (1   1   1) lattice planes with more terminal Cu atoms and V-CN with abundant nitrogen vacancies to form delocalized electronic structures like electronic reservoirs. This facilitates the wrapping of Cu 2 O octahedra by V-CN and protects their stability via tighter interfacial contact, thus enhancing the tunneling of carriers for rapid photocatalytic sterilization. These findings provide novel approaches for designing high-efficiency Cu 2 O-based photocatalytic antifoulants for practical applications.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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Foods · 2023 ·Vol. 12 ·期 4 ·707 · IF 5.2

A Novel Electrochemiluminescence Immunosensor Based on Resonance Energy Transfer between g-CN and NU-1000(Zr) for Ultrasensitive Detection of Ochratoxin A in Coffee

Linzhi Li,Xiaofeng Wang,Jian Chen,Tianzeng Huang,Hongmei Cao,Xing Liu

In this study, an electrochemiluminescence (ECL) immunosensor based on nanobody heptamer and resonance energy transfer (RET) between g-C3N4(g-CN) and NU-1000(Zr) was proposed for ultrasensitive ochratoxin A (OTA) detection. First, OTA heptamer fusion protein was prepared by fusing OTA-specific nanometric (Nb28) with a c-terminal fragment of C4 binding protein (C4bpα) (Nb28-C4bpα). Then, Nb28-C4bpα heptamer with the high affinity used as a molecular recognition probe, of which plenty of binding sites were provided for OTA-Apt-NU-1000(Zr) nanocomposites, thereby improving the immunosensors’ sensitivity. In addition, the quantitative analysis of OTA can be achieved by using the signal quenching effect of NU-1000(Zr) on g-CN. As the concentration of OTA increases, the amount of OTA-Apt-NU-1000(Zr) fixed on the electrode surface decreases. RET between g-CN and NU-1000(Zr) is weakened leading to the increase of ECL signal. Thus, OTA content is indirectly proportional to ECL intensity. Based on the above principle, an ultra-sensitive and specific ECL immunosensor for OTA detection was constructed by using heptamer technology and RET between two nanomaterials, with a range from 0.1 pg/mL to 500 ng/mL, and the detection limit of only 33 fg/mL. The prepared ECL-RET immunosensor showed good performance and can be successfully used for the determination of OTA content in real coffee samples, suggesting that the nanobody polymerization strategy and the RET effect between NU-1000(Zr) and g-CN can provide an alternative for improving the sensitivity of important mycotoxin detection.Keywords:Nb28-C4bpα heptamer;electrochemiluminescence immunosensor;resonance energy transfer;ochratoxin A

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ELECTROCHIMICA ACTA · 2020 · IF 6.215

Facile syntheses of bimetallic Prussian blue analogues (KxM[Fe(CN)6]·nH2O, M=Ni, Co, and Mn) for electrochemical determination of toxic 2-nitrophenol

Junhua Li,Lingzhi He,Jianbo Jiang,Zhifeng Xu,Mengqin Liu,Xing Liu,Haixia Tong,Zeng Liu,Dong Qian

In this work, three kinds of bimetallic Prussian blue analogues (PBAs), i.e. K x Ni [Fe(CN) 6 ]·nH 2 O (NiFe-PBA), K x Co [Fe(CN) 6 ]·nH 2 O (CoFe-PBA), and K x Mn [Fe(CN) 6 ]·nH 2 O (MnFe-PBA), were synthesized by a simple precipitation method under identical conditions. Their chemical compositions , structures, morphologies, valences of transition metals, and electrochemical sensing performances for 2-nitrophenol (2-NP) are examined in details. It is found that all the prepared PBAs hold face-centered-cubic structures with near perfect cube morphologies for NiFe-PBA and CoFe-PBA and truncated cube morphology for MnFe-PBA. For the electrochemical detection of 2-NP, a wide detection range of 1.0–700.0 μM was obtained at all PBAs modified electrodes together with the sensitivities of 443.3, 368.0, and 339.0 μA cm −2  mM −1 and detection limits of 0.28, 0.46, and 0.59 μM achieved at NiFe-PBA, CoFe-PBA, and MnFe-PBA modified electrodes, respectively. The superiority in electrochemical sensing performance of NiFe-PBA to CoFe-PBA and MnFe-PBA may stem from its higher conductivity, lager electroactive surface area, and better intrinsic catalytic property of the transition metal in its framework. Furthermore, the constructed NiFe-PBA-based sensor displays good repeatability, long-term stability, and high selectivity together with desirable recoveries (97.8–103.9%) for the assay of 2-NP in water samples. The present work is the first report on the PBAs-based electrochemical sensors for 2-NP detection, which may promise a future of PBAs or PBAs-based materials for sensing applications.

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ENERGY & FUELS · 2021 · IF 3.605

High-Performance Aqueous Sodium-Ion Battery Based on Graphene-Doped Na2MnFe(CN)6–Zinc with a Highly Stable Discharge Platform and Wide Electrochemical Stability

Manqi Zhang,Tianbao Dong,Degang Li,Kai Wang,Xuezhong Wei,Shaomin Liu

The development of aqueous sodium-ion batteries (ASIBs) has been greatly restricted as a result of their narrow electrochemical stability window (ESW) (about 1.23 V). Many researchers attempt to expand the ESW using high concentrations of electrolyte solution or choosing titanium or other inert materials as collectors. However, these methods would lead to higher battery costs. In this work, we demonstrated a low-cost ASIB system, in which the cathode, anode, and electrolyte solution were applied by graphene oxide (GO)-modified Na2MnFe(CN)6 (PBM), zinc sheet, and solution of Na2SO4 (1 M) and ZnSO4 (1 M), respectively. When the graphite sheet with high hydrogen and oxygen evolution overpotential was used as the collector, the ESW was expanded to about 3.4 V. The full cell owned a stable discharge platform and high discharge potential (∼1.8 V). Furthermore, the modification of PBM by reduced graphene oxide (rGO) obviously increased the discharge capacity to 110 mAh g–1, extended the cycle life (91% capacity retention after 200 cycles), and greatly improved the rate capacity (76% capacity for 500 mA g–1 rate). It should also be noted that the full cell consisting of a rGO/PBM cathode and zinc anode could achieve an energy density as high as 165 Wh kg–1.

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Electromagnetic bilayer composite film: Cocoa-tree-like FL and spiky-ball-like CN structures for superior electromagnetic shielding, thermal management, and strain sensing performance

Gengmei Liu,Jinbao Li,Dingwen Yin,Huijuan Xiu,Simin Wang,Xuanchen Jiang,Yuxin Qin,Feiguo Hua,Yufei Jia,Mengxia Shen

With the rapid development of flexible and integrated electronics, there is an urgent need for electromagnetic shielding materials that meet the requirements of thinness, high electromagnetic interference shielding effectiveness (EMI SE), and low reflection loss (SE R ). This study designs an FL/CN composite film with an electric–magnetic bilayer multiscale structure, constructing an “absorption-reflection–absorption” electromagnetic wave dissipation path. First, spiky-ball-like Ni nanoparticles (NiNPs) were grown on cellulose nanofibers (CNF) via in situ reduction to form a magnetic layer (CN). This layer generates hysteresis and resonance losses while leveraging its multi-wall effect to induce polarization, multiple reflections, and scattering losses. Second, a multi-dimensional nanostructured FL conductive layer was fabricated using a mechanical blending method. The conductive network of silver nanowires (AgNWs) provides conductive loss, and the cocoa-tree-like SiO 2 @PDA structure forms a “resistor–capacitor” circuit to generate polarization loss, further attenuating and reflecting electromagnetic waves. Finally, the abundant heterogeneous interfaces in the macroscopic bilayer structure enhance electromagnetic wave dissipation. As a result, the composite film achieves an exceptional EMI SE of 85.59 dB with a low SE R of only 7.73 dB, alongside a tensile strength of 23.67 MPa. Additionally, the film exhibits excellent flexibility (bending radius < 6 mm), thermal management performance (thermal conductivity of 2.84 W/m·K), and strain sensing capabilities (response time of < 400 ms). This study provides a novel and scalable approach for developing flexible thin film EMI shielding materials with high shielding effectiveness and low reflection, demonstrating significant advantages over existing technologies in terms of efficiency, flexibility, and multifunctionality.

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RSC Advances · 2015 ·Vol. 5 ·期 84 ·68815-68821 · IF 3.84

Fluorescent magnetic nanosensors for Zn2+ and CN− in aqueous solution prepared from adamantane-modified fluorescein and β-cyclodextrin-modified Fe3O4@SiO2 via host–guest interactions

Qiang Li,Yue Zhang,Yang Jin,Qingbiao Yang,Jianshi Du,Yaoxian Li

A novel multifunctional fluorescent chemosensor has been constructed with a highly selective “off–on” behavior, recoverability and recyclability based on β-CD/AD (adamantane) host–guest self-assembly interactions. Adamantane-modified fluorescein/cyclodextrin-modified Fe3O4@SiO2 inclusion complex magnetic nanoparticles (FFIC MNPs), which can provide a specific green fluorescence enhancement in response to Zn2+, have a detection limit of 4.5 × 10−7 mol L−1 in CH3CN : H2O (1 : 4, v/v). The spirolactam ring in the fluorophore moiety would be open with the introduction of Zn2+, while it could recover as long as the zinc in the complex is removed. Meanwhile, one gram of FFIC MNPs can adsorb 6.1 mg zinc. Therefore, the derivative chemosensors, FFIC MNPs–Zn, are available to respond to CN− due to the fluorescence quenching under UV (ultraviolet) radiation with a detection limit of 7.7 × 10−7 mol L−1. Furthermore, the FFIC MNPs exhibit great reusability and recyclability in aqueous solution on account of their magnetism and reproducibility. We recycle the residual MNPs to detect Zn2+ repeatedly for at least 4 times, after readily adsorbing the complex zinc with excess CN−, and the same principle also works in reverse. If the fluorophore moiety is inactive, we could also wash out the useless fluorescent molecules from the MNPs (hosts) and then reassemble new fluorescent small-molecules (guests) to maintain the efficient properties of the probe in responding to Zn2+ and CN− for at least 7 times.

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2024 · IF 7.7

Construction and evaluation of AuNPs enhanced electrochemical immunosensors with [Fe(CN)6]3−/4− and PPy probe for highly sensitive detection of human chorionic gonadotropin

Qi Zhao,Zhencheng Chen,Chen-Wei Shan,Tao Zhan,Chen-Yang Han,Guo-Cheng Han,Xiao-Zhen Feng,Heinz-Bernhard Kraatz

Human chorionic gonadotropin (HCG), a vital protein for pregnancy determination and a marker for trophoblastic diseases , finds application in monitoring early pregnancy and ectopic pregnancy . This study presents an innovative approach employing electrochemical immunosensors for enhanced HCG detection, utilizing Anti-HCG antibodies and gold nanoparticles (AuNPs) in the sensor platform. Two sensor configurations were optimized: BSA/Anti-HCG/c-AuNPs/MEL/e-AuNPs/SPCE with [Fe(CN) 6 ] 3−/4− as a redox probe (1) and BSA/Anti-HCG/PPy/e-AuNPs/SPCE using polypyrrole (PPy) as a redox probe (2). The first sensor offers linear correlation in the 0.10–500.00 pg∙mL −1 HCG range, with a limit of detection (LOD) of 0.06 pg∙mL −1 , sensitivity of 32.25 μA∙pg −1 ∙mL∙cm −2 , RSD <2.47 %, and a recovery rate of 101.03–104.81 %. The second sensor widens the HCG detection range (40.00 fg∙mL −1 -5.00 pg∙mL −1 ) with a LOD of 16.53 fg∙mL −1 , ensuring precision (RSD <1.04 %) and a recovery range of 94.61–106.07 % in serum samples. These electrochemical immunosensors have transformative potential in biomarker detection, offering enhanced sensitivity, selectivity , and stability for advanced healthcare diagnostics.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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BIOSENSORS & BIOELECTRONICS · 2025 · IF 10.5

Signal-amplified molecularly imprinted electrochemical sensor using Cu2Fe(CN)6/Cu-benzenehexathiol metal-organic framework for ultra-sensitive detection of methadone and its metabolite EDDP

Tong Dou,Junzheng Zhang,Wenzhen Yang,ShuaiTian Guo,Meng Zhang,Jingyi Wang,Zhizhen Xu,Dongsheng Wang

Methadone and its metabolite 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) are key biomarkers in wastewater-based epidemiology studies for assessing illicit opioid consumption. Due to their extremely low concentrations in wastewater, conventional laboratory-based detection methods are time-consuming, complex, and require expensive instrumentation, making them unsuitable for rapid on-site analysis. Herein, we developed a signal-amplified molecularly imprinted electrochemical sensor based on a Cu 2 Fe(CN) 6 /Cu-benzenehexathiol conductive metal-organic framework (CB-MOF) composite for the ultrasensitive detection of methadone and EDDP. The composite exhibits a high electrochemical signal through in situ synthesis of a conductive MOF with an integrated Prussian-Blue-analog redox probe. Guided by density functional theory (DFT) and molecular dynamics simulations, p-aminobenzoic acid (PABA) was selected as the functional monomer to construct a molecularly imprinted recognition layer for specific target binding. The sensor demonstrated a wide linear detection range for EDDP from 2.78 ng/L to 277.4 mg L −1 and methadone from 309.5 ng/L to 309.5 mg L −1 , with limits of detection as low as 99.86 pg/L and 3.28 ng/L, respectively. In addition, the sensor exhibited excellent stability, selectivity, reproducibility, regenerability, and applicability, offering robust support for the rapid on-site detection of opioids in municipal wastewater and river water.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 29 ·15543-15553 · IF 14.511

Simultaneous optimization of CoIr alloy nanoparticles and 2D graphitic-N doped carbon support in CoIr@CN by Ir doping for enhanced oxygen and hydrogen evolution reactions

Weibin Chen,Yuxin Xie,Xuehui Gao,Lei Li,Zhan Lin

Multiple electronic structure modification is propitious for constructing strong metal–support interaction and then improving the electrocatalytic activity of supported catalysts, yet remains a great challenge due to the lack of facile protocols. Herein, we report a CoIr alloy supported on two dimensional (2D) graphitic-N doped carbon (CoIr@CN) through a one-step annealing process from an Ir-doped 2D Co-MOF, which exhibits a remarkably reduced Ir loading (2.69 wt%) and enhanced electrocatalytic activity for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Ir plays an essential role of optimizing the properties of metal nanoparticles and simultaneously effecting the calcining process to adjust the N-doping structure, eventually modulating the synergetic effect between alloy nanoparticles and the N-doped carbon support. Owing to the positive effect of such multiple electronic structure optimization, the electron transfer between alloy nanoparticles and N-doped carbon is promoted to enable more moderate adsorption energies of reaction intermediates in both the OER and HER. Impressively, CoIr@CN exhibits a low OER/HER overpotential of 269 mV/70 mV to achieve a current density of 10 mA cm−2 in 1.0 M KOH, and 25 mV in 0.5 M H2SO4 for HER, as well as a negligible decay of catalytic activity after long-term stability measurements for OER/HER. This study offers an effective way for designing strong metal–support interaction through multiple electronic structure modification, which effectively improves the OER/HER performance of supported catalysts.

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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2020 · IF 3.306

Multi-responsive fluorescent probe based on AIE for the determination of Fe3+, total inorganic iron, and CN- in aqueous medium and its application in logic gates

Xiaoye Wen,Li Yan,Zhefeng Fan

A novel and simple probe (denoted LN-1) with AIE property based on malononitrile and 4-diethylaminobenzaldehyde was designed and synthesized. The use of two different mechanisms for the independent detection of Fe 3+ and CN − is more convenient and efficient than the continuous detection of anions and cations. The detection mechanism was verified by mass spectrometry (MS), nuclear magnetic resonance (NMR) spectrum, and particle size distribution. Under optimized experimental conditions, excellent calibration curves were obtained for the LN-1-Fe 3+ and the LN-1-CN − with detection limits of 0.17 and 0.39 μM, respectively. This method was successfully applied to detect the content of Fe 3+ and total inorganic iron in actual samples. Owing to its low cytotoxicity, good biocompatibility, and enhanced orange emission in aqueous solution, the LN-1 was successfully applied for CN − imaging in live cells. In addition, Fe 3+ and EDTA incorporation into the LN-1 changed the fluorescent intensity, which is beneficial in constructing ultrasensitive INHIBIT logic gate.

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EcoMat · 2024 · IF 10.7

Prussian blue analogs photocatalyst promote the evolution of value-added platform compounds via Co?CN?Zn covalent bonds

Junming Shi,Guoyang Gao,Can Jin,Hongqing Wu,Weizhen Wang,Yulong An,Zhen Zhou,Zhanhua Huang,Wenshuai Chen

Value-added conversion of lignocellulose is a sustainable approach. Photo-refining biomass is in line with current environmental protection strategies. However, photo-reforming biomass suffers from poor catalyst stability and low conversion efficiency. Here, we designed fructose as a lignocellulosic model. The heterogeneous structure of Prussian blue coating was constructed with a special covalent bond structure of Co  CN  Zn. This structure has a catalytic conversion mechanism that can accelerate electron transfer. Fructose was simultaneously converted to value-added platform compounds (5-HMF and formic acid) and gaseous fuels (CO, CH 4 ) with a conversion rate of up to 92.5%, which is more than 1.7 times than that of catalysts without adding Prussian blue. Hydrogen transfer and carbon transfer on the carbon atoms of fructose facilitates the production and accelerates the spillover of CO from formic acid. This work provides new ideas for the development of Prussian blue catalysts and the conversion of pentose.

CAS / MDL: 2386-53-0 7646-79-9
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