CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Yimin Zhang,Yonglin Ren,Yun Zu,Ke Yan,Yibin Luo,Enhui Xing,Yucai Qin,Yi Mei,Xingtian Shu
Available hierarchization and phosphorization of ZSM-5 zeolite as one of methanol-to-propylene (MTP) catalysts have improved reactive stability and propylene selectivity, but are subjected to the problems of poor phosphorus stabilization efficiency and inhomogeneous dispersion. Herein, we fabricate a series of hierarchical P@ZSM-5 zeolites via one-step disassembly-reassembly-phosphating strategy of ZSM-5 zeolite using successfully self-created asymmetric quaternary phosphonium hydroxides and elucidate the mechanism of mesoporous formation and the interaction of phosphorus with framework aluminum. Delightfully, reconstructively tetracoordinated P IV -O-Al IV structure endows excellent hydrothermal and Brønsted acid stability of hierarchical P@ZSM-5 zeolites. The MTP tests show that the P@ZSM-5(TBuCP) catalyst prepared by disassembly-reassembly-phosphating of tributylhexadecylphosphine hydroxide (TBuCPOH) exhibits superior propylene selectivity (48.9 %) and remarkedly long lifetime (32.5 h, WHSV=6h −1 ). Such enviable MTP performance is benefited from the join hands of the zeolitic hierarchization and suitable Brønsted acid strength conferred by its phosphorus-aluminum interaction that are conducive to olefinic cycle process. These findings afford value-filled opportunities in novel MTP catalysts with high reactive stability and propylene selectivity, and the understandings for phosphorus-zeolite chemistry.
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FOOD CHEMISTRY
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2024
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IF 8.5
Mingyue Ye,Xianfeng Lin,Jin Li,Xiaowan Chen,Dichen Ying,Shijia Wu,Zhouping Wang,Nuo Duan
Malachite green (MG) has been illicitly employed in aquaculture as a parasiticide, however, its teratogenic and carcinogenic effects pose a significant human health threat. Herein, a dual-mode colorimetric and electrochemical aptasensor was fabricated for MG detection, capitalizing on the robust catalytic and peroxidase-like activity of P-CeO 2 NR@Mxene and good capture efficiency of a tetrahedral DNA nanostructure (TDN) designed with multiple aptamers (m-TDN). P-CeO 2 NR@Mxene-modified complementary DNA (cDNA) served as both colorimetric and electrochemical probe. m-TDN was attached to AuE to capture MG and P-CeO 2 NR@Mxene/cDNA. The superior aptamer and MG binding to cDNA regulated signals and enabled precise MG quantification. The further introduced Exo I enabled aptamer hydrolysis, releasing MG for further binding rounds, allowing target recycling amplification. Under the optimal conditions, the aptasensor reached an impressively low detection limit 95.4 pM in colorimetric mode and 83.6 fM in electrochemical mode. We believe this dual-mode approach holds promise for veterinary drug residue detection.
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PubMed
高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2024
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IF 4.1
Yunhao Zhang,Yanxin Qiao,Yihui Wu
The development of efficient, inexpensive, and earth-abundant electrocatalysts for the oxygen evolution reaction (OER) represents a significant challenge for the large-scale production of hydrogen. The primary obstacle to the advancement of OER is the necessity for a considerably higher overpotential than the theoretical oxygen evolution potential, due to the sluggish kinetics of the electron transfer reaction, which involves a large amount of thermodynamic energy. In this article, amorphous and cauliflower-like Co-P electrocatalysts were in situ grown on nickel foam by dynamic hydrogen bubble template (DHBT) electrodeposition method. The Co-P electrocatalyst with Co/P ratio optimal presented excellent electrocatalytic activities with a low overpotential of 239 mV for OER at 10 mA·cm −2 and long-term stability in 1.0 M KOH. The outstanding OER performance of the catalyst is mainly attributed the synergistic effect of amorphous and cauliflower-like structure, superhydrophilicity surface, and the electronic regulation by adjusting the atomic ratio of Co to P. This research will bring fresh ideas and strategies for developing novel simple, affordable, and efficient electrocatalysts to boost OER kinetics.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2024
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IF 5.8
Jiang-Hao Lu,Ze Li,Di Zhang,Lu-Hang Song,Xiao-Yan Cai,Liang Mao,Zhi-Qiang Liu,Zhi-Jie Wang,Xiu-Quan Gu,Guo-Dong Yuan
The nano/microstructuring of silicon (Si) via chemical methods has garnered significant attention due to its excellent light-trapping capabilities across a wide spectral range. Current research has predominantly focused on the synthesis of pyramidal-shaped microtextures, which enable two reflections on the surface, while largely overlooking the superior light-trapping potential of inverted pyramid silicon (SiIP) microtextures, which theoretically allow for three reflections. Moreover, there has been limited investigation into the application of inverted pyramid black silicon for solar-driven hydrogen evolution. This study reports the synthesis of uniformly arranged inverted pyramid-textured black silicon using the copper-assisted chemical etching (Cu-ACE) method to enhance the efficiency of solar-driven water splitting for hydrogen production. The formation mechanism and the influence of copper-localized surface plasmon resonance (Cu-LSPR) from Cu nanoparticle (NP) byproducts on photoelectrochemical (PEC) activity were systematically analyzed. To reduce sidewall defects and minimize photogenerated carrier recombination, the surface of the SiIP was treated with tetramethylammonium hydroxide (TMAH). A vertical PN junction was developed through ion implantation to reduce the external bias of the SiIP. Additionally, a uniform TiO₂ antireflective layer was deposited via atomic layer deposition (ALD), reducing the average reflectance of the SiIP-T 4 to 5.78 % over the 300–1100 nm wavelength range. MoSₓ and Pt NPs were electrodeposited to improve the fill factor and enhance HER kinetics. With optimized catalyst loading, the n + p-SiIP-T 4 /TiO₂/Pt 80 mC electrode achieved a photocurrent density of 8.0 mA cm −2 at 0 V vs. RHE, an applied bias photon-to-current efficiency (ABPE) of 0.93 % at 0.24 V vs. RHE, and a double-layer capacitance (Cdl) of 91 μF cm −2 . The onset potential (Von) was positively shifted by ∼1.13 V to 0.49 V vs. RHE compared to a SiIP photocathode, and the photocathode operated continuously at 0 V vs. RHE for 27 h in an acidic electrolyte. These results demonstrate that SiIP has significant potential for PEC hydrogen evolution, with further performance optimization achievable through structural and surface engineering.
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POLYHEDRON
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2024
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IF 2.4
Muhammad Jamshaid,Adeel Ahmed,Rashid Iqbal,Ali Fareed,Wedad A. Al-onazi,Mohamed S. Elshikh
The current study focuses on the development of highly efficient nickel oxide/titanium dioxide (NiO/TiO 2 ) p-n heterojunction catalysts constructed via sol–gel and ultrasonic techniques. Different techniques, including XRD, SEM, EDS mapping, and XPS, confirmed the successful synthesis of the photocatalysts. The BET analysis showed that the NiO/TiO 2 heterojunction has a surface area of 107.52 m 2 /g compared to pure NiO and TiO 2 (75.37 m 2 /g and 89.13 m 2 /g) respectively. The catalyst was then implemented to decompose the antibiotic tetracycline (TC) in water under visible light. The outcomes revealed that the degradation rate of TC reached 97.69 % using NiO/TiO 2 , which is substantially greater than the degradation achieved with pure NiO (52.43 %) and TiO 2 (71.11 %) within a 48-minute period pursuant to the most favorable circumstances. The initial rate constant of the NiO/TiO 2 (0.0756 min −1 ) was significantly higher compared to that of the NiO (0.0153 min −1 ) and TiO 2 (0.0261 min −1 ). The lower bandgap energy of the NiO/TiO 2 (3.19 eV) catalyst compared to the pure NiO (3.58 eV) and TiO 2 (3.29 eV) facilitated the abatement of TC due to the improved harvesting of visible light absorption. Furthermore, the study investigated the impact of several different reaction parameters and intervening anions on TC degradation. Radical trapping investigations substantiate the existence of reactive oxygen species. In addition, NiO/TiO 2 catalyst exhibited extraordinary stability and maintained its catalytic efficiency despite enduring five successive cycles. Overall, the NiO/TiO 2 catalyst demonstrated remarkable potential for abolishing TC-contaminated water.
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Arabian Journal of Chemistry
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2024
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IF 5.3
Jin Liu,Qian Zhong,Yanjin Wang,Zezhi Zhang,Huiqin Zheng,Bin Yan,Yurong Shi
Designing photocatalysts with p-n heterojunction structures is an effective way to boost the separation of photogenerated carriers and stimulate the photocatalytic degradation activity. Herein, an efficient visible-light responsive AgI/BiSI p-n heterojunction photocatalyst was successfully constructed. X-ray photoelectron spectroscopy (XPS), photoluminescence (PL) spectroscopy, and electrochemical measurements confirmed that the AgI/BiSI p-n heterojunction structure was beneficial to the separation and transfer of photogenerated carriers, promoting the generation of main active species (•O 2 − and h + ). Furthermore, the photocatalytic degradation rate constants of Acid Red 1 (0.4699 min −1 ) and metronidazole (0.0730 min −1 ) over the optimal AgI/BiSI were about 8.4 and 3.0 times higher than those over pure AgI, respectively. This work provides a heterojunction engineering strategy to design high-efficient photocatalysts for the degradation of refractory organic pollutants.
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Environmental Science-Nano
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2017
·Vol. 4
·期 5
·1037-1044
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IF 6.047
Wen-Jing Wang,Jun-Mei Xia,Xin Hai,Ming-Li Chen,Jian-Hua Wang
The nucleophilic substitution reaction between 4-chloro-7-nitro-2,1,3-benzoxadiazole (NBD-Cl) and –NH2 groups on amino-functionalized carbon dots (CDs) produces a novel carbon dot-based hybrid, CDs@NBD for short. In addition to the characteristic fluorescence emission of carbon dots at λex/λem = 360/443 nm, the CDs@NBD hybrid gives rise to new photoluminescence at λex/λem = 460/544 nm, which is significantly quenched by p-phenylenediamine (PPD) via static quenching. This provides a novel sensing approach for fluorometric detection of PPD with CDs@NBD as a probe. A linear calibration graph is obtained within two concentration ranges of 0.1–1.0 μmol L−1 and 1.0–10.0 μmol L−1, along with a detection limit of 56 nmol L−1 and a RSD of <3% (at 1.0 μmol L−1). The common coexisting species in environmental and biological sample matrices cause no obvious interferences on the detection of PPD. The colour change of the CDs@NBD hybrid solution with the variation in PPD concentration also facilitates visual detection of PPD, which further demonstrates promising applications in environmental and biological sample analysis.
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DIAMOND AND RELATED MATERIALS
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2024
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IF 4.3
Yudan Wang,Xin Zhang,Xue Li,Yaru Jiang,Tianxin Shen,Jinsong Peng,Chunxia Chen,Dengfeng Yu,Gongyuan Zhao
Rechargeable aqueous zinc‑iodine batteries (ZIBs) with low environmental impact and abundant natural reserves have become promising electrochemical energy storage devices. However, the shuttle effect and low conductivity lead to poor electrochemical performance, hindering their practical applications. Herein, a (NH 4 ) 3 PO 4 -activated ZIF-8-derived porous carbon (NPPC) is proposed for entrapping iodine species in ZIBs. Benefiting from its abundant porous structure and highly conductive framework, the iodine loading and electron transport of NPPC is greatly enhanced. In addition, the in-situ doping multiple heteroatoms (N, P and O) in the carbon framework can also establish chemical anchoring with iodine species and hence mitigate the shuttle effect. As a result, the ZIBs prepared by the NPPC-1.5/I 2 electrode achieves an ultra-high specific capacity of 175 mAhg −1 at 0.1 A g −1 , and a specific capacity of 95 mAh g −1 at a high current density of 10 A g −1 . An extremely stable cycle performance of 97 % capacity retaining after 6000 cycles at 10 A g −1 is also obtained. This study provides a new strategy for realizing aqueous ZIBs with high capacity and long cycling life.
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NEW JOURNAL OF CHEMISTRY
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2024
·
IF 2.7
Guangyu Deng,Chunmiao Xia,Xiangyu Nie,Sheng Xu,Cuige Zhang,Yinsheng Fang,Rongli Zhang
Photocatalytic degradation is a promising way for removing industrial pollutants from wastewater. However, selective enrichment and removal of target pollutants especially at ultralow concentrations are extremely challenging. Herein, a highly selective and efficient strategy for photocatalytic degradation of an organic pollutant, p-nitrophenol (PNP), is developed based on photosensitive molecularly imprinted polymer nanoparticles and TiO2 photocatalyst functionalized fiberglass cloth (FGC). The negatively charged p-nitrophenol@photosensitive random copolymer nanoparticles (PNP@PAVE NPs) and the positively charged TiO2 NPs were used as building blocks to successively deposit on the surface of FGC, followed by the removal of the PNP through UV radiation, leading to the formation of PNP-MIP NP and TiO2 NP decorated FGC (TiO2/PNP-MIP NPs/FGC) with high selectivity and photocatalytic activity. As a result, TiO2/PNP-MIP NPs/FGC exhibited a removal rate of 98.7% and excellent selectivity for PNP. This work provides a valuable approach for realizing highly selective degradation of specific pollutants in complex pollutant mixtures in a real environment.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2025
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IF 5.4
Mengqi Bian,Rui Liu,Qinghai Zhang,Yunlong Qu,Guanghui Chen,Jihai Duan,Hui Zhao,Weiwen Wang
The one-step preparation of methacrylic acid from isobutylene presents a significant challenge. In this study, three-dimensionally ordered macroporous (3DOM) Mo-V-P-Ce was synthesized using the hard template method and employed as a carrier for heteropolyacids in the selective oxidation of isobutene (IBN) to produce methacrylic acid (MAA). The CuNH 4 PAV@3DOM Mo-V-P-Ce catalyst developed through this method exhibits an ordered macroporous structure, which significantly enhances its thermal stability. Additionally, it contains a significant number of active species (VO 2 + ) and appropriate moderately strong acidic centers, which collectively improve the overall performance of the catalyst. The combination of CuNH 4 PAV with the 3DOM structure increases the surface concentration of oxygen vacancy species, thereby promoting the catalytic activity of the composite catalyst in converting these oxygen vacancy species into lattice oxygen species. Notably, the selectivity of the synthesized heteropolyacid catalysts for MAA increased to 84 % after loading. This work offers a novel approach to the development of efficient catalysts.
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ADVANCED FUNCTIONAL MATERIALS
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2024
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IF 18.5
Hongkun Wang,Mingyu Du,Hao Jiang,Ruixuan Zhou,Yan Wang,Kunyan Sui,Wenxin Fan
Ionic diode-based generators show great superiority in harvesting low-frequency mechanical energy from human motions for various wearable applications. The major challenge is to improve their extremely limited output voltage for the miniaturization/simplicity of ionic diode-based self-powered devices as well as further improvement of mechanoelectric conversion performance. Herein, the construction of gradient polycation/polyanion heterojunction is demonstrated to vastly boost the output voltage, energy-harvesting efficiency, and sensing performance of ionic diode. Besides an inherent potential at the polyanion/polycation heterojunction interface, the additional transmembrane potentials can be generated across gradient polyanion and polycation conductors of ionic diodes due to their gradient charge distribution. Consequently, the gradient ionic diode-based generators produce much higher output voltage (306.53 mV) than previously reported homogeneous ones (4.1–135 mV). Meanwhile, the high output voltage imparts gradient ionic diode-based generator with ultrahigh power density (50.16 µW cm − 2 or 250.8 µW cm −3 ) and pressure-perception sensitivity (43582 mV/MPa), which are dramatically increased by 162.76% and 128.71%, respectively, compare to those of homogeneous one. Impressively, the resulting diode-based generators can generate ultralarge current density (≈0.52 mA cm −2 ) with ultralong discharge time (>400 s), thus enabling the continuous power generation under the low-frequency pressure for various wearable and implantable applications.
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Journal of Energy Storage
·
2024
·
IF 8.9
Qinlian Liu,Xiaojie Tan,Xudong Li,Yiwen Li,Xuan Han,Shihao Cui,Dejian Xu,Yachao Liu,Rui Wang,Qingshan Zhao,Mingbo Wu
Transition metal selenides (TMSs) have emerged as promising electrode materials for potassium-ion batteries (PIBs), whereas the large volume expansion and sluggish reaction kinetics have seriously hindered the cycle life and rate performance. Herein, a hierarchical composite of flower-like CoSe 2 /N, P-doped carbon microspheres accommodated on carbon nanosheets (CoSe 2 -NPC@CNS) was rationally fabricated as the anode for PIBs through a one-pot hydrothermal and subsequent selenization method. The intimate hybridization of CoSe 2 /N, P-doped carbon microspheres can effectively alleviate the volume expansion of CoSe 2 during charge-discharge cycles, and the ultrathin carbon nanosheets derived from fluid catalytic cracking (FCC) slurry serves as a highly conductive and buffered substrate. By robustly merging them together, the interconnected hierarchical nanoarchitecture with exposed active sites achieves promoted potassium storage capacity, electrochemical reaction kinetics, and structural stability. As a result, the PIBs with CoSe 2 -NPC@CNS anode deliver high reversible capacities of 320.8 mAh g −1 after 100 cycles at 0.1 A g −1 and 213.9 mAh g −1 after 850 cycles at 1.0 A g −1 , excellent rate capability (188.8 mAh g −1 at 5 A g −1 ), and enhanced pseudo-capacitive contribution rate of 88.7 %. This work offers valuable insight into the rational design and development of hierarchical anode materials with high performance for PIBs and beyond.
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