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ACS Omega · 2022 · IF 4.132

Core–Shell Polydopamine/Cu Nanometer Rods Efficiently Deactivate Microbes by Mimicking Chloride-Activated Peroxidases

Lian-Jiao Zhou,Yu-Ying Wang,Shu-Lan Li,Ling Cao,Feng-Lei Jiang,Thomas Maskow,Yi Liu

Cu-modified nanoparticles have been designed to mimic peroxidase, and their potent antibacterial and anti-biofilm abilities have been widely investigated. In this study, novel core–shell polydopamine (PDA)/Cu4(OH)6SO4 crystal (PDA/Cu) nanometer rods were prepared. The PDA/Cu nanometer rods show similar kinetic behaviors to chloride-activated peroxidases, exhibit excellent photothermal properties, and are sensitive to the concentrations of pH values and the substrate (i.e., H2O2). PDA/Cu nanometer rods could adhere to the bacteria and catalyze hydrogen peroxide (H2O2) to generate more reactive hydroxy radicals (•OH) against Staphylococcus aureus and Escherichia coli, Furthermore, PDA/Cu nanometer rods show enhanced catalytic and photothermal synergistic antibacterial activity. This work provides a simple, inexpensive, and effective strategy for antibacterial applications.

CAS / MDL: 62-31-7 54827-17-7
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Acta Biomaterialia · 2021 · IF 8.947

Pd-Cu nanoalloy for dual stimuli-responsive chemo-photothermal therapy against pathogenic biofilm bacteria

Zefeng Wang,Yanling Peng,Yan Zhou,Shengnan Zhang,Jianxi Tan,Huan Li,Dinggeng He,Le Deng

Photothermal therapy (PTT) is a promising strategy for antimicrobial therapy. However, the application of PTT to treat bacterial infections remains a challenge as the high temperature required for bacterial elimination can partly damage healthy tissues. Selecting the appropriate treatment temperature is therefore a key factor for PTT. In this work, we designed a near-infrared/pH dual stimuli-responsive activated procedural antibacterial system based on zeolitic imidazolate framework-8 (ZIF-8), which was bottom-up synthesized and utilized to encapsulate both Pd-Cu nanoalloy (PC) and the antibiotic amoxicillin (AMO). This procedural antibacterial therapy comprises chemotherapy (CT) and PTT. The former disrupts the bacterial cell wall by releasing AMO in an acidic environment, which depends on the sensitive response of ZIF-8 to pH value change. With the progression in time, the AMO release rate decreased gradually. The latter can then significantly stimulate drug release and further complete the antibacterial effect. This impactful attack consisted of two waves that constitute the procedural therapy for bacterial infection. Accordingly, the treatment temperature required for antibacterial therapy can be significantly lowered under this mode of treatment. This antibacterial system has a significant therapeutic effect on planktonic bacteria (G + /G − ) and their biofilms and also has good biocompatibility; thus, it provides a promising strategy to develop an effective and safe treatment against bacterial infections. Statement of Significance We have developed a near infrared/pH dual stimuli-responsive activated procedural antibacterial system that combines enhanced antibiotic delivery with photothermal therapy and has highly efficient antimicrobial activity . The antibacterial effect of this therapy was based on two mechanisms of action: chemotherapy, in which the bacterial cell wall was first destroyed, followed by photothermal therapy. After exposure to irradiation with an 808 nm laser, the inhibition rates were 99.8% and 99.1% for Staphylococcus aureus and Pseudomonas aeruginosa , respectively, and the clearance rates for their established biofilms were 75.3% and 74.8%, respectively. Thus, this procedural antibacterial therapy has shown great potentiality for use in the photothermal therapy of bacterial infectious diseases, including biofilm elimination.

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ACS Omega · 2022 · IF 4.132

Boosting Hydrogen Evolution through the Interface Effects of Amorphous NiMoO4–MoO2 and Crystalline Cu

Yue Yao,Enlai Hu,Zhiyu Wang,Yuanjing Cui,Guodong Qian

The rational design and synthesis of a highly efficient and cost-effective electrocatalyst for hydrogen evolution reaction (HER) are of great importance for the efficient generation of sustainable energy. Herein, amorphous/crystalline heterophase Ni–Mo–O/Cu (denoted as a/c Ni–Mo–O/Cu) was synthesized by a one-pot electrodeposition method. Thanks to the introduction of metallic Cu and the formation of amorphous Ni–Mo–O, the prepared electrocatalyst exhibits favorable conductivity and abundant active sites, which are favorable to the HER progress. Moreover, the interfaces consisting of Cu and Ni–Mo–O show electron transfers between these components, which might modify the absorption/desorption energy of H atoms, thus accelerating HER activity. As expected, the prepared a/c Ni–Mo–O/Cu possesses excellent HER performance, which affords an ultralow overpotential of 34.8 mV at 10 mA cm–2, comparable to that of 20 wt % Pt/C (35.0 mV), and remarkable stability under alkaline conditions.

CAS / MDL: 7791-20-0 333-20-0
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JOURNAL OF POROUS MATERIALS · 2021 ·Vol. 29 ·期 2 ·371-380 · IF 2.496

Direct synthesis of Cu-containing Beta zeolite without template for selective oxidation of cyclohexane

Zhang Wei,Xue Haonan,Wang Min,Wu Zeying,Ding Linlin,Deng Yaoyao,Wang Wei,Wei Xuejiao,Zhang Zhenwei,Xiang Mei

Cu-containing Beta zeolites (Cu-Beta) are straightforwardly synthesized in a one-pot method without template, where the crucial step is the co-hydrolysis/condensation of silica source and copper salt at the moderate acidic condition. In the solvent-free oxidation of cyclohexane with molecular oxygen (O 2 ), the best cyclohexane conversion result (9.7%) with a KA-oil (cyclohexanone and cyclohexanol) selectivity of 94.1% is obtained over Cu-Beta(100). Structure—activity relationship analysis indicates that the isolated tetrahedral framework Cu 2+ species and chemisorption oxygen species in high concentration on the catalyst surface enhannce the catalic performance. In addition, the catalyst can be easily separated and still remain stable after recycling five times, providing new insights into catalysts design for the catalytic oxidation of cyclohexane to KA-oil.

CAS / MDL: 7758-99-8
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2021 · IF 4.539

Superhydrophilic/underwater superaerophobic self-supporting CuS/Cu foam electrode for efficient oxygen evolution reaction

Ya-li Yao,Jin-mei He,Xin Yang,Lei Peng,Xue-dan Zhu,Kan-she Li,Meng-nan Qu

Hydrogen production by electrochemical overall water splitting is an economic and green approach to resolve the looming energy and environmental crisis. However, the electrocatalytic oxygen evolution reaction (OER) generally occurs at low rate due to the delayed reaction kinetics of four-electron transfer. Herein, a kind of crater-like micro-nano structure CuS three-dimensional electrode that was supported on a Cu foam was prepared and used as an electrode anode for overall water splitting. The superhydrophilic/underwater superaerophobic structure can significantly reduce the bubble adhesion on the electrode surface and improve the OER performance. The CuS/CF electrode showed good wettability and superaerophobicity with an underwater contact angle of 153.5°. The CuS/CF (CuS/Cu foam) electrode has been proved to have excellent electrocatalytic activity for water decomposition. In 1.0 M KOH solution, the OER overpotential is 350 mV at 10 mA cm −2 and the Tafel slope is 83 mV dec −1 . In acidic medium of 0.5 M H 2 SO 4 solution, the overpotential of hydrogen evolution (HER) is 134 mV at 10 mA cm −2 and the Tafel slope is 114 mV dec −1 . The underwater superaerophobic electrode still has strong stability after 10 h test. This work provides a new potential electrochemical catalyzed approach to water decomposition by constructing a super-infiltration electrode.

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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2021 · IF 7.664

Highly efficient MXene/Nano-Cu smoke suppressant towards reducing fire hazards of thermoplastic polyurethane

Yongqian Shi,Chuan Liu,Libi Fu,Yuezhan Feng,Yuancai Lv,Zixiao Wang,Minghua Liu,Zhixin Chen

A large number of toxic fumes evolved from polymeric materials are a great threat to human evacuation. The aim of this work is to dramatically reduce the generation of smoke and toxic gaseous products upon polymers burning. A highly efficient titanium carbide/nano-copper (Ti 3 C 2 T x /Nano-Cu) hybrid smoke suppressant was synthesized by interficial adhesion and then incorporated into thermoplastic polyurethane (TPU) to fabricate TPU nanocomposites. The Ti 3 C 2 T x /Nano-Cu hybrid was homogeneously dispersed in the TPU matrix and showed a strong interfacial interaction with the TPU host. Introducing the Ti 3 C 2 T x /Nano-Cu hybrid into TPU led to enhanced high-temperature stability. Furthermore, the smoke production rate, CO production rate and total CO yield of the TPU nanocomposite containing 2 wt% Ti 3 C 2 T x /Nano-Cu hybrid decreased by 66.7%, 51.8% and 52.9%, respectively, compared with those of pure TPU. The reduced fire hazards of the TPU were due to the physical barrier, the catalytic charring and the chemical conversion of Ti 3 C 2 T x /Nano-Cu hybrid.

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ACS Omega · 2021 · IF 3.512

Fabrication of Superhydrophobic SA-CeO2@Cu Mesh and Its Application in Oil–Water Separation

Ting Liang,Biao Wang,Zhenzhong Fan,Qingwang Liu

CeO2 was synthesized by the co-precipitation method on the Cu mesh substrate and modified the surface of CeO2@Cu mesh by stearic acid (SA). The superhydrophobic behavior was ascribed to the combination of hierarchical micro–nanostructure of CeO2 and the hydrophobic alkyl groups from SA. The SA-CeO2@Cu mesh had antiacid and base stability and excellent durability as well as high separation efficiency. The separation efficiency can be up to 98.0% after separating 30 times.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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MICROCHEMICAL JOURNAL · 2021 · IF 4.821

Determination of peracetic acid by an Ag nanoparticle decorated Cu-organic framework modified electrode

Wenzhi Zhang,Tian Jiang,Xiuxiu Sun,Ani Zhou,Maoguo Li

Peracetic acid (PAA) is commonly used as the strong oxidant in many areas. However, high concentration of PAA can be harmful to health of people. The quantitative determination of PAA is of great significance. Here, a metal–organic framework (MOF) is introduced into the electrochemical sensor for PAA detection. The influence of common transition metal centers on the performance of electrochemical detection of PAA was investigated and the results showed the Cu-1,3,5-trimesic acid (Cu-BTC) was the best original MOF. Ag nanoparticles were decorated in the Cu-BTC to further improve the electrocatalytical activity. The concentration of the added Ag salt and the quality of the reducing agent tannic acid (TA) had a great impact on the performance. The final sample optimized for the synthesis conditions was named as Ag NPs/Cu-BTC. The electrochemical sensor based on Ag NPs/Cu-BTC/GCE was fabricated for sensing PAA with a wide linear range (0.1–5000 μM), low detection limit (0.046 μM, S/N = 3) and high sensitivity (1013.4 μA mM −1 cm −2 ). The water stability of Ag NPs/Cu-BTC and the anti-interference ability of the sensor were good. The electrochemical sensor could be applied in detecting the concentration of PAA in the commercially available peracetic acid, suggesting the practical application value.

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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

Unveiling the water-resistant mechanism of Cu(I)-O-Co interfaces for catalytic oxidation

Shuaiqi Zhao,Peng Wu,Jiajin Lin,Yifei Li,Anqi Li,Xiaojing Jin,Yu Chen,Bote Zhao,Yun Zhao,Guangxu Chen,Yongcai Qiu,Daiqi Ye,Shihe Yang

The development of low-temperature and water-resistant heterogeneous catalysts without noble metals is vital in the effective treatment of atmospheric pollutants in practical application. Herein, we report that Cu(I)-O-Co interfaces of ultrafine CuO x on Co 3 O 4 prepared by co-precipitation exhibit promising low-temperature activity and good water resistance. Experiment results together with density functional theory (DFT) calculations not only verify that Cu + species are stabilized over Cu(I)-O-Co interfaces because of the strong interaction between Cu 2 O 1 and Co 3 O 4 , but also demonstrate that the Cu(I)-O-Co interface facilitates oxygen species activation for promoting catalytic oxidation and reduces the accumulation of hydroxyl and bicarbonate species on the surface of CuO x /Co 3 O 4 . DFT calculations also reveal that the CO oxidation rate-limiting step via the dissociation pathway under dry conditions is the Co-OO-Cu species dissociation while the CO coupling with the adsorbed O 2 becomes the rate determining step for CO oxidation through the direct pathway over Cu(I)-O-Co interface under humid conditions. Further, the CuO x /Co 3 O 4 catalyst also exhibits superior and stable catalytic activity for toluene oxidation, comparable with partial supported noble metal catalysts (T 90  = 190 °C). The present work gives a useful strategy for the rational design of low-temperature and water-resistant non-precious-based catalysts to be applicable in CO and toluene removal in practical applications.

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JOURNAL OF ALLOYS AND COMPOUNDS · 2021 · IF 5.316

Self-supported hierarchical P,Cu-codoped cobalt selenide nanoarrays for enhanced overall water splitting

Yong Wang,Shouzhu Li,Dafeng Zhang,Fang Tan,Lei Li,Guangzhi Hu

Highly efficient electrocatalysts with low cost for electrochemical water splitting is important for the intermediate energy conversion. In the present work, P and Cu dual-doped cobalt selenide nanoarrays with hierarchical structure were fabricated via a facile hydrothermal method, involving in-situ growth on a self-supported conductive Ni foam substrate (P,Cu-Co 0.85 Se/NF). The overall water splitting (OWS) performance of the catalysts was systematically studied in alkaline solution. Compared to single-ion-doped or pure Co 0.85 Se, dual incorporation of the anion and cation can contort the lattice and induce powerful electronic interactions, thereby exposing abundant catalytic sites and optimizing the adsorption energy of the reaction intermediates. Benefiting from the merits of P, the Cu-co-doped Co 0.85 Se/NF electrode exhibited outstanding catalytic activity towards hydrogen evolution reaction (HER), generating a 10 mA cm −2 current density at the overpotential of 96.8 mV in 1 M KOH, and the overpotential is 300 mV towards oxygen evolution reaction (OER) with the current density of 100 mA cm −2 . Furthermore, when applied it to fabricate OWS cell, the cell voltage is as low as 1.57 V at the current density of 10 mA cm −2 . This present work broaden the potential application of the electrocatalytic performance of transition metal dichalcogenides .

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Nanoscale · 2021 ·Vol. 14 ·期 5 ·1796-1806 · IF 7.79

MOF-derived electrochemical catalyst Cu–N/C for the enhancement of amperometric oxygen detection

Wenyan Yin,Milin Zhang,Jingyuan Liu,Khaled Tawfik Alali,Jing Yu,Jiahui Zhu,Peili Liu,Rumin Li,Jun Wang

Electrochemical sensors using ionic liquids as electrolytes for oxygen detection are now getting more and more attention. Recently, an ionic liquid combined with an electrochemically active catalyst system has become popular for boosting the sensing performance of oxygen sensors. In this work, the imidazolyl-based ionic liquid 1-butyl-2,3-dimethylimidazole bis((trifluoromethyl)sulfonyl)imide [Bmmim][TFSI] is first prepared by a facile two-step method. Subsequently, a transition metal and N-codoped porous carbon oxygen reduction electrochemical catalyst Cu–N/C is synthesized by calcining the Cu-doped ZIF-8 precursor and then blending it in different ratios with the ionic liquid [Bmmim][TFSI] as composite electrolytes for oxygen detection. The composite electrolyte Cu–N/C/[Bmmim][TFSI] exhibits increased responses in cyclic voltammetry (CV) and chronoamperometry (CA) relative to that of the pure ionic liquid. Furthermore, the CV and CA data show that 6% Cu–N/C/[Bmmim][TFSI] has the optimum oxygen sensing response with an enhanced reduction peak current, a sensitivity of 0.1678 μA/[% O2] and a good linear fitting coefficient of 0.9991. In conclusion, the results confirm the success of using Cu–N/C as an electrochemical catalyst composed of the Cu–N/C/[Bmmim][TFSI] electrolyte for improving the responsivity, stability and sensitivity towards a wide range of oxygen concentrations.

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SEPARATION AND PURIFICATION TECHNOLOGY · 2021 · IF 7.312

Cu-TCPP nanosheets blended polysulfone ultrafiltration membranes with enhanced antifouling and photo-tunable porosity

Shabab Hussain,Xinyi Wan,Zhuoyi Li,Xinsheng Peng

The major obstacle in membrane filtration technology is the membrane fouling, which not only decreases the membrane efficiency, but also enhances its operational cost. In order to fabricate a membrane with antifouling characteristics, potential nanofillers have been added to the engineering polymer(s) to make a composite to improve the membrane efficiency. Herein, we incorporate porphyrin-based ultrathin, highly ordered porous photothermal responsive copper tetrakis(4-carboxyphenyl)porphyrin (Cu-TCPP) nanosheets as a novel nanofillers into the polysulfone (PSf) matrix. High loading (6 wt%) and well dispersed Cu-TCPP nanosheets incorporated polysulfone nanocomposite (Cu-TCPP/PSf) ultrafiltration membranes are prepared via non-solvent induced phase inversion. The Cu-TCPP/PSf composite membranes demonstrate pronounced antifouling and antibiofouling potential along good separation performance. The nanocomposite membranes demonstrate photo-induced pore tuning due to the local heating of photothermal Cu-TCPP nanosheets by visible light, which further improves the membrane separation efficiency. The Cu-TCPP/PSf composite membrane with 6 wt% Cu-TCPP nanosheets enhances the pure water permeance from 23.42 to 260.61 L·m −2 ·h −1 ·bar −1 , with improved antifouling potential, precise permeance recovery ratio of 99.13% after three cycles, and good separation performance for 100 and 200 nm particles. Considering relatively moderate cost, facile processing, tunable porosity, durable and good mechanical strength along restrained swelling, the Cu-TCPP/PSf membranes are considered as potential candidate as antifouling/antibiofouling ultrafiltration membranes for water purification.

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