CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Yi Fang,Shoubing Chai,Zhiwei Chu,Zirui He,Yingjie Li
In the calcium looping CO 2 capture process, using CO in the flue gas to reduce NO at a high molar ratio of CO to NO (e.g., above 10:1) can achieve efficient removal of NO. However, the lots of unreacted CO causes secondary pollution. In this study, a novel Cu/Ce co-modified CaO was proposed for cyclic CO 2 capture and the catalytic NO reduction at a low CO:NO molar ratio (e.g., 2:1). The experimental findings indicate that Cu/Ce modification improves the performance of CaO in both catalytic NO reduction and carbonation. The Cu/Ce co-modified CaO contained the optimal Cu/Ce/Ca molar ratio of 1:5:100 possesses both NO removal and CO conversion efficiencies of above 99 %, along with CO 2 removal efficiency exceeding 88%. Microscopic analysis determines that the electron transfer between Cu and Ce facilitates the conversion of lattice oxygen into surface oxygen, mitigating the competition between CO 2 and CO for surface oxygen. Furthermore, density functional theory calculations demonstrate that CO/NO/CO 2 exhibits non-competitive adsorption behavior on Cu/Ce co-modified CaO. Consequently, Cu/Ce-modified CaO possesses superior catalysis for efficient NO reduction by CO at low CO:NO molar ratio in calcium looping process.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Chen Wang,Xiaohui Wu,Mingjie Huang,Tao Zhou,Juan Mao,Xiangling Zhang
Treatment of Cr(VI)-contaminated wastewaters by conventional reduction methods has been intensively challenged by alkaline environments. In this study, a novel copper-iron oxide composite (Cit@CuFeO) enriched with oxygen vacancies (OVs) was developed by ball milling with citric acid ligand (Cit). The material demonstrated efficient Cr(VI) removal within a broad pH range (6.0–12.0). Intriguingly, simultaneous and nearly complete in-situ immobilization of Cr(III) occurred, instead of precipitated in strong alkaline circumstances. Characterizations of the Cit@CuFeO revealed that ball milling of Cit could introduce abundant OVs into the oxide structure, serving as pivotal active sites linearly correlated with Cr(VI) capture and removal. These generated OVs could also boost electron conduction in Cit@CuFeO and cause a positive shift in the zeta potential , thereby enabling the adsorption of negative CrO 4 2- at high pH. Furthermore, DFT calculation verified that the surface-attached Cit would significantly decrease the adsorption energy of Cr(VI) at OVs sites, competitively excluding the occupancy of common inorganic anions especially CO 3 2– and thus favoring the Cr(III) immobilization under alkaline conditions. This study has provided a green functional material for the one-step remediation of alkaline Cr(VI) wastewaters without the need for acidification.
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ENVIRONMENTAL POLLUTION
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2024
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IF 7.6
Yaoyu Zhou,Jianlong Wang
Electro-Fenton (EF) can in-situ produce H 2 O 2 and effectively activate H 2 O 2 to generate powerful reactive species for the destruction of contaminants under acidic conditions, however, the production of iron-containing sludge and requirement of low working pH significantly hinder its practical application. Herein, a novel Cu, N co-doped carbon (Cu–N@C) with metal organic framework (MOF) as a precursor was constructed and adopted for the elimination of pefloxacin (PEF) in the heterogeneous electro-Fenton (HEF) process. PEF could be almost completely removed within 1 h and total organic carbon (TOC) removal efficiency was 48.57% within 6 h. Meanwhile, Cu–N@C had good repeatability and environmental adaptability, it can still maintain excellent catalytic performance after 10 cycles, and it exhibited satisfactory remediation performance in simulated water matrix. In addition, the HEF process catalyzed by Cu–N@C also showed satisfactory degradation effect on other organic pollutants including atrazine, methylene blue, and chlorotetracycline. Under the action of impressed current, the HEF system could generate H 2 O 2 in-situ, and the active species could be generated in the redox cycle of Cu 0 /Cu 1+ /Cu 2+ . Electron paramagnetic resonance and quenching experiments confirmed that •OH was the dominant active species in the degradation of organic compounds. The degradation process of PEF was studied by mass spectrometry analysis of intermediate products. This study provided a simple method to prepare MOF-based electrocatalyst , which exhibits promising application potential for treatment wastewater .
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Nature Communications
·
2024
·Vol. 15
·期 1
·1-22
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IF 14.7
Bai Mingru,Wang Ting,Xing Zhenyu,Huang Haoju,Wu Xizheng,Adeli Mohsen,Wang Mao,Han Xianglong,Ye Ling,Cheng Chong
The clinical treatments of maxillofacial bone defects pose significant challenges due to complex microenvironments, including severe inflammation, high levels of reactive oxygen species (ROS), and potential bacterial infection. Herein, we propose the de novo design of an efficient, versatile, and precise electron-donable heterojunction with synergetic Ru-Cu pair sites (Ru-Cu/EDHJ) for superior biocatalytic regeneration of inflammatory mandible defects and pH-controlled antibacterial therapies. Our studies demonstrate that the unique structure of Ru-Cu/EDHJ enhances the electron density of Ru atoms and optimizes the binding strength of oxygen species, thus improving enzyme-like catalytic performance. Strikingly, this biocompatible Ru-Cu/EDHJ can efficiently switch between ROS scavenging in neutral media and ROS generation in acidic media, thus simultaneously exhibiting superior repair functions and bioadaptive antibacterial properties in treating mandible defects in male mice. We believe synthesizing such biocatalytic heterojunctions with exceptional enzyme-like capabilities will offer a promising pathway for engineering ROS biocatalytic materials to treat trauma, tumors, or infection-caused maxillofacial bone defects.
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ACS Catalysis
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2024
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IF 11.3
Heng Cao,Xiaodi Zhu,Jiawei Xue,Ruyang Wang,Jiusi Shang,Peiyu Ma,Chengyuan Liu,Jun Bao
Precise design of photocatalysts with the demanded active surface structure for highly efficient and selective CO2 photoreduction is crucial but challenging. Here, by taking CdS as a prototype, single-atom Cu is successfully constructed on Cd-deficient CdS (Cd1–xS) to improve the performance of CO2 photoreduction with H2O as proton donor. The optimal Cu/Cd1–xS with Cd vacancies (VCd)-mediated single-atom Cu exhibits nearly 100% selective CO production and a more than three-fold higher CO evolution rate compared to that of Cd1–xS. Both experimental identification and DFT theoretical simulation unveil that the VCd-mediated single-atom Cu render Cu–S pair sites to function as more catalytically active sites for dissociating H2O and promoting the corresponding proton supply, which favors the subsequent protonation of the adsorbed CO2 at the adjacent Cd sites via the two-proton coupled two-electron transfer pathway. This work demonstrates the importance of modulating proton supply from the oxidation half-reaction for facilitating the overall CO2 photoreduction, advocating an overall-reaction perspective for the design and development of highly efficient and selective CO2 conversion photocatalysts.
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
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2025
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IF 8.3
Liang Chen,Jialin Zhao,Jinlong Li,Yan Zhuang,Dongxuan Guo,Shuang Meng,Dantong Zhang,Xue Yang,Guozhe Sui
Bimetallic-organic frameworks and their derivatives have attracted intensive attention in the field of photocatalytic hydrogen production due to their high porosity, distinctive three-dimensional structure, and favorable specific surface area. Despite these advantages, the efficiency of photocatalytic hydrogen production remains unsatisfactory owing to rapid complexation of electron-hole pairs and limited visible light utilization. Herein, in this work, the autogenous CuO–ZnO heterojunction nanoparticles are assembled on the surface of reduced graphene oxide (RGO) by calcining copper-zinc bimetallic-organic frameworks. The autogenous heterojunctions offer numerous active sites and enhance electron transfer at tightly bound heterogeneous interfaces. Furthermore, RGO acts as a co-catalyst or substrate, improving photocatalytic performance with its high surface area and excellent electron transport properties. Consequently, the RGO/CuO–ZnO Z-scheme heterojunction achieves an impressive hydrogen production rate of 479.73 μmol g −1 h −1 , which is 94.06 times higher than that of pristine ZnO. Overall, this work optimizes the potential of metal-organic framework-derived photocatalysts in hydrogen production and offers valuable insights into the effective construction of autogenous heterojunctions.
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ADVANCED FUNCTIONAL MATERIALS
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2024
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IF 18.5
Jiahui Yan,Haoyu Chen,Carlos F. Guimarães,Rui L. Reis,Zhihua Zhu,Tianyi Wang,Fenglan Zhang,Yaqian Lv,Qihui Zhou,Xiaoying Kong,Jinsheng Shi
Ion interference including copper (Cu + )/calcium (Ca 2+ ) overload activate cell-specific death channels, damage mitochondria and disrupt cellular homeostasis, showing great potential in anti-tumor therapy. However, the complex metabolic environment and the powerful self-protection of tumors cause clinical failure of ion interference. Thus, metabolic disruption is expected an innovative strategy for the enhancement of ion interference. Herein, CuS-α-CHCA&penthiopyrad@CaCO 3 -RGD nanoparticles (CCPCR NPs) are prepared to provide a Cu + /Ca 2+ dual-overload anti-tumor therapy assisted by metabolic-symbiosis-destruction strategy, realizing the collapse of tumor self-protection. Specifically, precise CuS and CaCO 3 delivery triggered irreversible Cu + /Ca 2+ dual-overload and reactive oxygen species (ROS) attack toward 4T1 cells. Meanwhile, α-CHCA and penthiopyrad disturbed the metabolic symbiotic environment by disrupting the TCA cycle and preventing lactate efflux to aggravate intracellular acidosis and promote Fenton-like reaction of Cu + , enhancing the sensitivity of tumor cells to copper death and Ca 2+ overload. Further, aided by the metabolism of symbiosis, the destroyed tumor cells further activate the polarization of M1 macrophages and the maturation and antigen cross-presentation of dendritic cells (DCs), which further eliminate tumor cells. In summary, an amplified anti-tumor dual-ion interference strategy assisted by metabolic symbiotic destruction is established, which is of great significance in improving the clinical effect of ion therapy for tumors.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2024
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IF 8.1
Guanli Chen,Defu Yao,Zheling Wang,Ketong He,Hong Xia,Fushen Lu,Muwei Ji,Ziyi Zhong,Yibing Song
Cuprous oxide (Cu 2 O), which has an appropriate band gap, is widely used as a marine antifouling biocide. This makes it increasingly valuable for photocatalytic antibacterial applications. Using crystal engineering technology to create Cu 2 O with tailored Cu 2 O/Cu interfaces and crystal planes can effectively enhance its performance but presents challenges. Herein, we report a simple wet chemical method for the controlled preparation of Cu 2 O@Cu hollow heterostructure. Experimental results demonstrate that the prepared composites exhibited highly efficient and broad-spectrum photocatalytic antibacterial effects against both Gram-negative and Gram-positive bacteria, achieving 100% antibacterial efficiency under 10 min of irradiation, much more effective than the bulk Cu 2 O. Characterization results show that a hollow spherical structure consisted of fine Cu 2 O@Cu nanoparticles in their wall, and the generated interfaces facilitated the migration and separation of photogenerated charge carriers and promoted the formation of hydroxyl radicals with stronger oxidizing abilities. Meanwhile, the Cu outside layer of each Cu 2 O@Cu particle not only acted as a shield to protect Cu 2 O from corrosion but also served as an electron acceptor to efficiently transfer photogenerated electrons, thereby demonstrating highly effective and stable antibacterial performance. This study not only offers a valuable reference for developing highly efficient and universal photocatalytic materials but also provides insight into the chemical reaction in the photocatalytic antibacterial process.
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
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2025
·Vol. 26
·期 2
·569
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IF 4.9
Jieni Wang,Xiaobo Han,Shuqin Zhang,Haodong Hou,Chenlin Wei,Chenxiao Liu,Leichang Cao,Jinglai Zhang,Li Wang,Shicheng Zhang
It is challenging to handle heavy-metal-rich plants that grow in contaminated soil. The role of heavy metals in biomass on the physicochemical structure and electrochemical properties of their derived carbon has not been considered in previous research. In this study, Cu-ion hybrid nanoporous carbon (CHNC) is prepared from Cu content-contaminated biomass through subcritical hydrocharization (HTC) coupling pyrolytic activation processes. The CHNCs are used as advanced electrode material for energy storage applications, exhibiting an impressively ultrahigh capacitance of 562 F g−1at a current density of 1 A g−1(CHNC-700-4-25), excellent energy density of 26.15 W h kg−1, and only 7.59% capacitance loss after enduring 10,000 cycles at a current density of 10 A g−1, making CHNCs rank in the forefront of previously known carbon-based supercapacitor materials. These comprehensive characterizations demonstrate that copper ions introduce new electrochemically active sites and enhance the conductivity and charge transport performance of the electrode material, elevating the specific capacitance of CHNC from 463 to 562 F g−1. These findings offer valuable insights into the effective energy storage application of heavy-metal-contaminated biomass wastes.
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Journal of the Taiwan Institute of Chemical Engineers
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2024
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IF 5.5
Fengyi Wang,Xiangji Li,Jiahao Liu,Jianqiang Wang,Jinghui Zhang,Hongtao Chen
Background The demand for high-power density packaging and integration processes for third-generation semiconductors, like silicon carbide (SiC), necessitates advancements beyond conventional Si-based packaging technologies. Cu-Cu direct bonding emerges as a promising alternative in semiconductor packaging. However, achieving Cu-to-Cu direct bonding with low-temperature, low-pressure, and short-time poses significant challenges. Transient Liquid Phase Bonding (TLP) offers a low-temperature joining solution, but prolonged reflow time hinders its wide applications. Methods This study introduces a novel strategy utilizing bicontinuous microemulsion (BME) electrodeposition to fabricate micron-sized Cu arrays, addressing these challenges in achieving Cu bonding. The core of Cu array manufacturing lies in the differential electrodeposition rate of Cu ions in the aqueous and organic phases. This principle is rooted in the excellent conductivity of the aqueous solution compared to the non-conductivity of the organic solution. Significant findings We elucidate the growth mechanism and validate a theory for achieving void-free optimal growth of Cu arrays within BME and compared the cross-sectional morphology and fracture modes of TLP solder joints with micron and nano Cu arrays. Furthermore, the ability to recycle the BME soft template aligns with green chemistry principles, offering a sustainable die-attach approach for third-generation semiconductor device packaging.
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ENVIRONMENTAL RESEARCH
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2025
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IF 7.7
Yaning Yang,Haiyang Wang,Yan Zhu,Yan Ding,Jun Zheng,Fengyu Zan
The rapid spread of microbial contamination and drug-resistant bacteria poses a significant threat to ecosystems and public health, highlighting the urgent need for efficient and stable disinfection materials. Metal-organic frameworks (MOFs) have emerged as promising functional materials for a variety of applications due to their regular microstructure and excellent physicochemical properties. However, their long-term use is limited by intrinsic instability. In this study, we designed copper nanolayers as protective armor for titanium-based MOFs (Cu/Ti-MOFs) to enhance their catalytic performance in photocatalytic disinfection under visible-light irradiation. The results demonstrated that Cu/Ti-MOFs exhibited slightly improved antimicrobial activity against Escherichia coli (E. coli) , Staphylococcus aureus , and tetracycline-resistant E. coli compared to Ti-MOFs. More importantly, Cu/Ti-MOFs retained 92 % of their initial activity after seven consecutive catalytic cycles, whereas Ti-MOFs completely lost their photosensitive properties, indicating much higher catalytic stability of Cu/Ti-MOFs. This improvement was confirmed through various physicochemical characterizations and was attributed to the protection of active sites, catalyst reinforcement, and efficient surface reconstruction due to the introduction of the Cu nanolayer. This study provides a strategy for enhancing the long-term performance of MOF materials in photocatalytic water disinfection applications.
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ACS Applied Nano Materials
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2024
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IF 5.3
Peng Bo Niu,Yong Qiong Wang,Rong Hu,Tong Yang
With the improvement of the quality of life, the assessment of total antioxidant capacity (TAC) has attracted much attention in the field of a healthy diet, food analysis, or health guidelines. In this work, Cu nanoparticles (NPs)/CoO/carbon nanofibers (CNFs) as a promising nanozyme for peroxidase (POD) mimicking was synthesized by electrospinning and carbonation. Subsequently, a colorimetric sensing platform is constructed for TAC assessment by using 3,3′,5,5′-tetramethylbenzidine (TMB) as a chromogenic substrate based on Cu NPs/CoO/CNFs under presence of H2O2. The enhanced POD catalytic efficiency of Cu NPs/CoO/CNFs for TMB oxidation (ox-TMB) was about 3.2-fold higher than that of bare Cu NPs/CNFs or CoO/NFs, which was ascribed to the synergistic catalytic effect and the generation of heterogeneous interfaces between Cu NPs and CoO in CNFs. When some antioxidants such as AA, FA, TA, and GA were introduced in the chromogenic system, ox-TMB was reduced to colorless TMB, allowing the subsequent assessment of TAC. The results show that the limits of detection toward AA, FA, TA, and GA were 8.7, 8.3, 2.7, and 2.4 μM, respectively. Moreover, this proposed method was used for the TAC assay in real samples including fresh juices and commercial beverages, which showed good promise in practical applications such as food nutrition assessment, food analysis, personalized nutrition intervention, or staple food research.
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