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COLLOIDS AND SURFACES B-BIOINTERFACES · 2021 · IF 5.268

CeO2 QDs anchored on MnO2 nanoflowers with multiple synergistic effects for amplified tumour therapy

Yuyan Yan,Yafei Hou,Huijun Zhang,Wenqing Gao,Renlu Han,Jiancheng Yu,Long Xu,Keqi Tang

Chemodynamic therapy (CDT) is an emerging tumour-specific therapeutic technology. However, the relatively insufficient catalytic activity of CDT agents in the tumour microenvironment (TME) limits their biomedical application. In addition, severe hypoxia and glutathione (GSH) overexpression in the TME greatly limit the antitumour efficiency of monotherapy. Herein, a cancer cell membrane-camouflaged and ultrasmall CeO 2 -decorated MnO 2 (mMC) composite is developed for amplified CDT, photodynamic therapy (PDT) and photothermal therapy (PTT). Due to the homotypic targeting ability of cancer cell membranes, mMC nanoparticles preferentially accumulate in tumour tissue. In the TME, CeO 2 acts as a highly efficient CDT agent to convert endogenous H 2 O 2 to toxic reactive oxygen species (ROS) for killing cancer cells. Meanwhile, MnO 2 irradiated with near-infrared (NIR) light displays prominent hyperthermia and ROS generation performance to perform PTT and PDT. Moreover, MnO 2 can produce oxygen to ameliorate hypoxia and deplete GSH to relieve the antioxidant capability of tumours, which is beneficial to the simultaneous augmentation of PDT and CDT. Most importantly, the catalytic activity of CeO 2 was greatly improved by hyperthermia. Consequently, a significantly enhanced therapeutic efficiency was obtained by the above multiple synergistic effects. This work provides a proof of concept for amplified tumour therapy by synchronously self-supplying oxygen, consuming GSH, and enhancing catalytic activity.

研究领域: 生物医学工程 · 肿瘤治疗研究
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Triggering dual-mode dynamic optical responses by anchoring carbon dots on MnO2 hollow spheres

Sisi Li,Yajing Cai,Jiaying Situ,Biwen Wang,Beichen Ying,Jin He,Zhao-Qing Liu,Jianle Zhuang,Yibo Chen

Multi-mode responsive optical materials with versatile application prospects for optical sensing, optoelectrical devices, and information encryption are highly desired. Here we integrate fluorescent carbon dots onto the hollow MnO 2 spheres, and modulate the interaction between them to achieve a water-stimulated responsive system with dual-mode dynamic signals in both fluorescence and structural color. The composite film shows a structural color shifting from blue to green as well as displays a fluorescence “on” in the presence of trace water, with both changes capable of being reversibly switched up to 10 times. The amide bond between the two components enables the controllable dispersion and aggregation of the carbon dots which is essential to the reversibility. Fabrication of several security labels with separate information in structural color and fluorescence channels demonstrates the application potential of the composite. This work provides a concise route to develop new multi-mode responsive optical materials for applications in anti-counterfeiting, sensing, and coding.

研究领域: 材料科学 · 光学工程 · 纳米技术
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SEPARATION AND PURIFICATION TECHNOLOGY · 2025 · IF 9

Cs3Bi2Br9/MnO2 S-scheme hybrid with multimodal catalytic behavior for photothermal synergistic CO2 reduction under UV–visible-infrared light

Chao Du,Yunfei Ge,Junyi Qian,Zhijie Zhang

Solar-driven CO 2 conversion into reusable carbon forms is an attractive strategy to. reduce CO 2 emissions and provide feedstocks for industrial production. However, most of present catalysts suffer from poor light utilization and rapid charge recombination, thus severely restricting the efficiency of CO 2 photoreduction. Herein, an innovative strategy of integrating Cs 3 Bi 2 Br 9 and MnO 2 via self-assembly was established, with the aim of designing a multimodal photothermal catalyst for CO 2 reduction under full spectrum. In this hybrid, MnO 2 could combine with CBB to create an S-scheme photocatalyst with promoted carrier separation, and simultaneously acted as a “heater” to facilitate CO 2 photoreduction by effective photothermal conversion. Upon UV–vis-NIR illumination, the CBB/MnO 2 hybrid presented an impressively high CO production rate (R CO  = 189.75μmol g −1 h −1 ). Theoretical calculations combined with experimental tests indicated that the excellent catalytic activity of CBB/MnO 2 could be ascribed to the synergetic effect of greatly increased carrier transfer and high photothermal conversion efficiency, resulting in considerably enhanced solar-light-driven photothermocatalysis with no extra heat input. The as-proposed catalyst in this study provides a novel and effective approach to develop highly efficient photothermal catalysts for solar-to-fuel applications.

CAS / MDL: 1313-13-9
研究领域: 催化化学 · 环境科学 · 材料科学
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Journal of Energy Storage · 2024 · IF 8.9

Layered MnO2@PDA as cathode material toward high-performance aqueous zinc-ion batteries

Haiyang Li,Menglei Wang,Xinyu Lei,Boyou Hu,Hanlu Zhang,Yutong Xing,Meng Zhang

Aqueous zinc-ion batteries (AZIBs) can benefit from a deep understanding of the electrochemical reaction mechanism of cathode materials, which can assist in resolving issues such as cathode dissolution and electrostatic interactions. We reported a straightforward two-step synthesis of polydopamine coated MnO 2 (MnO 2 @PDA) and revealed the energy storage mechanisms in AZIBs. The layered structure of MnO 2 creates a generous passage for the insertion of H + /Zn 2+ ions. Simultaneously, the plethora of functional groups within PDA exerts a robust desolvation effect, bolstering the transfer rate of H + /Zn 2+ . This effect significantly enhances the overall efficiency and performance of cathode. The AZIBs, incorporating MnO 2 @PDA cathode material, consequently exhibit a satisfactory cycling capacity (412 mAh g −1 at 0.1 A g −1 ) and a superb specific energy (561.6 Wh kg −1 at 136.34 W kg −1 ). This work provides a new path for design strategies and catalytic mechanisms of MnO 2 @PDA cathode.

CAS / MDL: 872-50-4 7722-64-7
研究领域: 材料科学 · 电化学 · 能源存储
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JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART B-APPLIED BIOMATERIALS · 2018 ·Vol. 106 ·期 7 ·2544-2552 · IF 3.373

Self-production of oxygen system CaO2/MnO2@PDA-MB for the photodynamic therapy research and switch-control tumor cell imaging

Chenhui Ji,Zhongzhong Lu,Yonghui Xu,Beibei Shen,Shiyong Yu,Dan Shi

Photodynamic therapy (PDT) holds promise in biochemical study and tumor treatment. A novel multifunctional nanosystem CaO 2 /MnO 2 @polydopamine (PDA)-methylene blue (MB) nanosheet (CMP-MB) was designed. CaO 2 nanoparticles were encapsulated by MnO 2 nanosheet, and then PDA was coated on the surface of CaO 2 /MnO 2 nanosheets, which could adsorb photosensitizer MB through hydrophobic interaction or π-π stacking. In this nanosystem, CaO 2 /MnO 2 had the ability of self-production of oxygen, which solved the problem of tumor hypoxia largely. Moreover, it is worth mentioning that the fluorescence of MB was suppressed by MnO 2 , while its emission was triggered in the simulated tumor microenvironment. Therefore, CMP-MB nanosheet could be used to switch-control cell imaging potentially. 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyltetrazolium bromide testing and Live/Dead assay confirmed CMP-MB nanosheet had fewer side effects without illumination while it destroyed Hela cell with the illumination of light. Vitro cell experiment demonstrated CMP-MB nanosheet could achieve tumor microenvironment responsive imaging and inhibit tumor cell growth under illumination effectively. Therefore, the system has great potential for PDT application and switch-control tumor cell imaging. © 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2544–2552, 2018.

研究领域: 生物医学工程 · 肿瘤学 · 材料科学
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Journal of Materials Chemistry A · 2015 ·Vol. 3 ·期 31 ·16168-16176 · IF 7.443

Synthesis of an ε-MnO2/metal–organic-framework composite and its electrocatalysis towards oxygen reduction reaction in an alkaline electrolyte

Hao Wang,Fengxiang Yin,Biaohua Chen,Guoru Li

An ε-MnO2/metal–organic-framework (Fe) (i.e., ε-MnO2/MOF(Fe)) composite was synthesised by integrating ε-MnO2 and a MOF(Fe) support. The composite was characterised using X-ray diffraction, N2 adsorption–desorption, field emission scanning electron microscopy, transmission electron microscopy, elemental mapping, Fourier transform infrared spectroscopy, Raman spectroscopy and X-ray photoelectron spectroscopy. The ORR activity of the composite was evaluated by cyclic and linear sweep voltammetries in an alkaline electrolyte. The results revealed that in the ε-MnO2/MOF(Fe) composite, ε-MnO2 is in the form of nanorods, each with one end protruding and the other firmly anchored on the MOF(Fe) matrix with a high porosity and a high specific surface area. This unique structure of the composite is advantageous for oxygen diffusion and contact with ε-MnO2 during reactions, resulting in much better ORR activity and stability than those of ε-MnO2 in an alkaline electrolyte. The ε-MnO2/MOF(Fe)-catalysed ORR favours an apparent 4-electron transfer pathway in which oxygen was first reduced to hydroperoxide, which was further chemically decomposed into primarily OH− and O2.

研究领域: 材料化学 · 电化学 · 纳米催化 · 能源材料 · 无机功能材料
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RSC Advances · 2019 ·Vol. 9 ·期 56 ·32889-32897 · IF 3.049

MnO2/ZnCo2O4 with binder-free arrays on nickel foam loaded with graphene as a high performance electrode for advanced asymmetric supercapacitors

Wanjuan Cong,Rui Miao,Bairui Tao,Fengjuan Miao

ZnCo2O4 nanosheets were successfully arrayed on a Ni foam surface with graphene using a hydrothermal method followed by annealing treatment; then MnO2 nanoparticles were electrodeposited on the ZnCo2O4 nanosheets to obtain a synthesized composite binder-free electrode named MnO2/ZnCo2O4/graphene/Ni foam (denoted as MnO2/ZnCo2O4/G/NF). After testing the binder-free composite electrode of MnO2/ZnCo2O4/G/NF via cyclic voltammetry, galvanostatic charge–discharge and electrochemical impedance spectroscopy testing, we found that it exhibited ultrahigh electrochemical properties, with a high specific areal capacitance of 3405.21 F g−1 under a current density of 2 A g−1, and wonderful cycling stability, with 91.2% retention after 5000 cycles. Moreover, an asymmetric supercapacitor (ASC) based on MnO2/ZnCo2O4/G/NF//G/NF was successfully designed. When tested, the as-designed ASC can achieve a maximum energy density of 46.85 W h kg−1 at a power density of 166.67 W kg−1. Finally, the ASC we assembled can power a commercial red LED lamp successfully for more than 5 min, which proves its practicability. All these impressive performances indicate that the MnO2/ZnCo2O4/graphene composite material is an outstanding electrode material for electrochemical capacitors.

研究领域: 材料科学 · 电化学
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ACS Applied Materials & Interfaces · 2022 · IF 10.383

Multifunctional MnO2/Ag3SbS3 Nanotheranostic Agent for Single-Laser-Triggered Tumor Synergistic Therapy in the NIR-II Biowindow

Qian Wang,Botao Qu,Juan Li,Yuqin Liu,Jie Dong,Xiaoyang Peng,Ruiping Zhang

Regulating the level of reactive oxygen species (ROS) in a tumor is an efficient and innovative anticancer strategy. However, the therapeutic efficacy of ROS-based therapies, such as chemodynamic therapy (CDT) and photodynamic therapy (PDT), offers finite outcomes due to the oxygen dependence and limited concentration of hydrogen peroxide (H2O2) and overexpression of glutathione (GSH) within the tumor microenvironment (TME), so a single therapeutic strategy is insufficient to completely eliminate tumors. Therefore, we demonstrated an omnipotent nanoplatform MnO2/Ag3SbS3 (abbreviated as MA) with strong optical absorbance in the NIR-II biowindow and oxygen self-sufficient ROS-mediated ability, which not only relieves tumor hypoxia significantly but also enhances the photothermal therapy (PTT)/PDT/CDT efficacy. By 1064 nm laser irradiation, MnO2/Ag3SbS3 nanoparticles (NPs) reveal a favorable photothermal conversion efficiency of 23.15% and achieve a single-laser-triggered NIR-II PTT/PDT effect, resulting in effective tumor elimination. Once internalized into the tumor, MnO2/Ag3SbS3 NPs will be degraded to Mn2+ and Ag3SbS3. The released Ag3SbS3 NPs as a NIR-II phototherapy agent could be utilized for photoacoustic imaging-guided NIR-II PDT/PTT. Mn2+ could be used as a Fenton-like catalyst to continuously catalyze endogenous H2O2 for generating highly virulent hydroxyl radicals (•OH) for CDT and O2 for PDT, enhancing the efficiency of PDT and CDT, respectively. Meanwhile, Mn2+ realizes magnetic resonance imaging-guided accurate tumor therapy. Moreover, the MnO2/Ag3SbS3 NPs could deplete intracellular GSH in TME to promote oxidative stress of the tumor, further strengthening ROS-mediated antitumor treatment efficacy. Overall, this work presents a distinctive paradigm of TME-responsive PDT/CDT/PTT in the second near-infrared biowindow by depleting GSH and decomposing H2O2 for efficient and precise cancer treatment.

研究领域: 生物医学工程 · 癌症治疗 · 纳米医学
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ACS Applied Materials & Interfaces · 2025 · IF 8.2

Multifunctional Superhydrophobic Sponge In Situ Anchoring of Ag-MnO2 via Polydopamine Activation for Efficient Oil–Water Separation, Photothermal Conversion and Antibacterial Applications

Jundong Zhu,Fan Yang,Chongwen Jiang,Zhonghua Li,Yanfang Zhou,Xin Li

Frequent oil spills and the discharge of oily wastewater pose serious threats to the environment, ecosystems, and humans. Herein, a multifunctional superhydrophobic sponge was successfully prepared through the in situ growth of Ag-MnO2 nanoparticles assisted by polydopamine rapid deposition and subsequent hydrophobic silicon modification. Owing to the synergistic effects of the hierarchical micro/nanostructure and methyl-terminated surface modification, the obtained superhydrophobic sponge has a water contact angle (WCA) of 156.5°, demonstrating excellent chemical stability and structural durability under harsh environmental media and mechanical damage. For oil–water separation, the adsorption capacity of modified sponge for various oils ranges from 58.2 to 132.6 times its own weight and great separation efficiency up to 98.38%. Through the photothermal conversion effect of Ag-MnO2 nanocomposite, the surface temperature of the material can reach 64.1 °C under simulated radiation, achieving rapid adsorption and recovery of high-viscosity oil. Additionally, the immobilization of silver nanoparticles within the sponge skeleton effectively inhibits the growth of Escherichia coli and Staphylococcus aureus, exhibiting antibacterial properties that facilitate the elimination of bacteria in organically contaminated water sources. Therefore, the multifunctional superhydrophobic sponge in this study provides high potential and efficient application for efficient oil–water separation, rapid crude oil recovery, and antibacterial pollution of water.

研究领域: 环境科学 · 材料科学 · 生物医学
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FOOD CHEMISTRY · 2021 · IF 7.514

Nanozyme-strip based on MnO2 nanosheets as a catalytic label for multi-scale detection of aflatoxin B1 with an ultrabroad working range

Xinfa Cai,Meijuan Liang,Fei Ma,Zhaowei Zhang,Xiaoqian Tang,Jun Jiang,Can Guo,Sherif Ramzy Mohamed,Amira Abdel Goda,Dawood H. Dawood,Li Yu,Peiwu Li

Lateral flow immunoassay (LFIA) is the most effective real-time detection method for aflatoxin B 1 (AFB 1 ). Here, we constructed a nanozyme-strip based on MnO 2 nanosheets (MnO 2 NSs) as a catalytic label for detection of AFB 1 . By taking advantage of the MnO 2 -TMB catalytic amplified system, the new test achieves rapid detection with high sensitivity and ultrawide range. The limit of detection of the assay was 15 pg mL −1 , which was over 100-fold lower than the maximum limit set by the European Union (EU) of AFB 1 in foods. In addition, the strip test could offer 7 dynamic detection ranges, spanning 4 orders of magnitude, which could cater to the varieties of limits on AFB 1 residues in foods and feeds set by different countries. The estimated recoveries were in the range of 85.67%-106.38% with coefficients of variations (CVs) less than 9.68%. Overall, the developed approach is a rapid, reliable, sensitive and widely available tool for on-site detection of AFB 1 .

CAS / MDL: 3317-61-1 2564-83-2
研究领域: 食品安全检测 · 生物化学 · 纳米技术
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Advanced Materials Interfaces · 2021 ·Vol. 8 ·期 11 ·2100178 · IF 6.147

ZIF-67 Loaded on Fe3O4-MnO2 as Efficient Peroxymonosulfate Activator for Rapid Degradation of Carbamazepine

Limei Dong,Yiming Li,Xiuping Chen,Dan Zhang,Yihao Guan

Poor sorption capacity and low biodegradability of carbamazepine (CBZ) lead to the difficulties in CBZ removal from water. Sulfate radical-based advanced oxidation process shows great potential for organic pollutant removal. Metal organic frameworks (MOFs) demonstrate great potential in catalytic field due to their excellent properties. Hence, cobalt-based metal organic framework (ZIF-67) nanoparticles are loaded on Fe 3 O 4 -MnO 2 composite, and then this composite is applied as peroxymonosulfate (PMS) activator for CBZ degradation. The prepared catalyst exhibits excellent catalytic performance because of the central metal cobalt of ZIF-67 and the synergistic effect between MnO 2 and ZIF-67. 81% of CBZ with a high initial concentration of 20 mg L −1 is rapidly removed from water within 2.5 min. The prepared catalyst can be convenient to recycle under magnetic field while maintaining its high catalytic stability. Degradation mechanism analysis indicates that both • OH and SO 4 •− contribute to CBZ degradation, but SO 4 •− is the main radical species. XPS spectra reveal that Co(II)/Co(III), Mn(II)/Mn(III)/Mn(IV), and Fe(II)/Fe(III) are involved in PMS activation. The degradation pathway is put forward based on the detection of intermediates. This study provides a new inspiration for the fabrication of magnetic metal oxide-MOFs catalysts with outstanding recycling performance for PMS activation.

研究领域: 环境科学 · 催化 · 水处理
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Efficient activation of peroxymonosulfate by amorphous MnO2/α-Fe2O3 for the degradation of organic pollutants

Ronghao Wu,Xin Hu,Yihui Li,Yongfu Li,Yanjiang Cai,Peikun Jiang,Bing Yu

Constructing bimetallic nanostructures with specific crystalline phases provides an attractive strategy to develop highly efficient catalysts and explore structure-dependent catalytic properties. Herein, a new iron-based bimetallic catalyst consisting of amorphous MnO 2 and crystalline α-Fe 2 O 3 was synthesized for peroxymonosulfate (PMS) activation, named as a-MnO 2 /α-Fe 2 O 3 . The results show that the removal efficiency of sulfamethoxazole is over 90% within 120 min by the a-MnO 2 /α-Fe 2 O 3 in the presence of PMS at broad pH conditions ranging from 3 to 9. Furthermore, a complete degradation of bisphenol A (BPA) is achieved within 2 min in the a-MnO 2 /α-Fe 2 O 3 /PMS system under optimum conditions, and the BPA degradation rate constant of 1.67 min −1 outperforms most reported Fe- and Mn- based catalysts. The results of electron paramagnetic resonance analysis, quenching tests and Raman spectroscopy analysis show that the mechanism for the a-MnO 2 /α-Fe 2 O 3 -based PMS activation is dominated by the formation of activated surface-PMS complexes. ≡Mn(Ⅳ)–OH and ≡Fe(III)–OH of a-MnO 2 /α-Fe 2 O 3 are active sites for PMS adsorption to form inner-sphere complexes (≡Mn(Ⅳ)-OOSO 3 - ) through the replacement of surface hydroxyl groups. Finally, the a-MnO 2 /α-Fe 2 O 3 exhibits a remarkable removal efficiency of over 99% for BPA in column-bed tests conducted over 600 cycles, demonstrating its immense potential for practical applications.

CAS / MDL: 80-05-7
研究领域: 环境科学 · 催化 · 材料科学 · 化学工程
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