APPLIED SURFACE SCIENCE
·
2022
·
IF 7.392
Congyue Zhao,Chunling Li,Minghui Chen,Tianqi Niu,Qian Zhao,Tianjun Ni,Dong Yan,Weidong Wu,Dong Liu
The exploitation of an efficient way to treat antineoplastic doxorubicin hydrochloride (DOX) is critical due to its harmful effects on the ecological system and human health. Recently, photocatalysis has emerged as one of the most feasible strategies to resolve this crisis. However, the development of novel catalysts with highly efficient photocatalytic activity still remains a great challenge. Herein, a novel 0D/3D Nb 2 O 5 QDs/C-doped g-C 3 N 4 type-II heterojunction with outstanding adsorption and photocatalytic degradation capacities for DOX was developed based on combining elemental doping, morphological design and heterojunction fabrication. The C-doping significantly promotes the visible light response and charge migration of g-C 3 N 4 , thus benefiting to the removal of DOX. Meanwhile, the 0D/3D heterogeneous morphology endows the catalysts with abundant active sites, high adsorptive capacity, favourable structural stability, high surface area and enhanced charge migration, which all contribute to the excellent adsorption and photocatalytic performance. The superoxide radicals shown a prominent role in the photocatalytic reaction. In addition, the Toxicity Estimation Software Tool, liquid chromatography-mass spectrometry and density functional theory calculations were also employed to investigate the DOX degradation mechanism, possible pathways and corresponding toxicity of intermediates. This work provides a promising way to develop highly efficient catalysts for the degradation of DOX.
研究领域:
环境科学
·
材料科学
·
毒理学
✓ 已验证
DOI
高影响因子
MICROCHEMICAL JOURNAL
·
2025
·
IF 5.1
Wei Zhang,Min Chen,Xinjian Cheng,Jie Yang,Jumei Li
In this study, we demonstrated an efficient solar photocatalyst, g-C 3 N 4 modified hollow Ag/ZrO 2 core–shell composites (Ag/hZrO 2 /CN) using polymethylacrylic acid (PMAA) nanospheres as sacrificial template. The optimized Ag/hZrO 2 /CN catalyst demonstrated substantial photocatalytic performance, achieving 97.6 % degradation of methylene blue (MB) and 99.5 % degradation of thiram (TRM) within 90 min under simulated sunlight using a 500 W Xe lamp. The improved property is likely attributed to the synergistic effect among three constituents and the effective segregation of photogenerated electron-hole pairs in ZrO 2 , g-C 3 N 4 and Ag NPs, as confirmed by photocurrent and EIS analysis. Based on free radical scavenging studies (e − , h + , OH and O 2 − ), the mechanism underlying the boosted photocatalytic activity was suggested. Moreover, Ag/hZrO 2 /CN presented excellent surface enhanced Raman scattering activity, achieving quantitative sensing of MB and TRM with limits of detection of 5 × 10 −8 and 10 −6 mol/L, respectively, and a favorable linear correlation between SERS intensities and logarithmic concentration (R 2 ≥ 0.97). Additionally, Ag/hZrO 2 /CN accomplished recyclable SERS detection of MB and TRM through stimulated sunlight irradiation, which is significant for the recyclable SERS detecting through fast sunlight-powered procedure.
研究领域:
材料科学
·
环境科学
·
分析化学
✓ 已验证
产品关联
DOI
高影响因子
Journal of Physical Chemistry C
·
2023
·
IF 3.7
Jiahui Li,Dongwei Ma,Gui Lu,Dong Fu,Carlos Ponce de León,Jia Hong Pan
Al-ion batteries (AIBs) represent promising multivalent-ion battery alternatives to Li-ion batteries (LIBs). Exploration of cathode materials is the key to improving the electrochemical performance of AIBs. Here we demonstrate a promising AIB cathode candidate based on two-dimensional graphitic carbon nitride (g-C3N4) nanosheets with reversible de/embedding of [AlCl4]− anions in its special layered porous structure during the cyclic charge/discharge process. To address the sluggish ion/charge transportation kinetics that is inherently present in AIBs due to the intrinsically low conductivity of g-C3N4, we optimize different synthetic precursors of g-C3N4 including dicyandiamide, urea, and melamine and, further, develop a facile method for uniformly coating a N-doped carbon (N–C) coating layer on the optimal g-C3N4 derived from dicyandiamide. The resultant AIBs consisting of the g-C3N4@N–C cathode and Al metal anode in the AlCl3/[EMIm]Cl electrolyte exhibit an initial capacity of ∼54.9 mAh·g–1 at 0.2 C with a high Coulomb efficiency ∼99.9%, and they possess long-term cycling over 200 cycles. The underlying charge/discharge process of AIBs, revealed by the ex situ X-ray diffraction and scanning electron microscopy analyses, involves the extraction/insertion of Al species (mainly Al3+, AlCl4–, and Al2Cl7–) into the g-C3N4 crystal lattices with the formation of intermediate Al8C3N4 and (ClCN)3.
研究领域:
材料科学
·
电化学
✓ 已验证
DOI
高影响因子
ENVIRONMENTAL RESEARCH
·
2021
·
IF 6.498
Hui Zhao,Cheng Tian,Jian Mei,Shijian Yang,Po Keung Wong
Two different morphologies of Fe 2 O 3 involving nanodots and nanosheets were deposited on g-C 3 N 4 nanosheets by simple in-situ deposition and impregnation-hydrothermal methods, respectively. Structural effect of Fe 2 O 3 on photo-Fenton-like activity and charge transfer at the interface in these two g-C 3 N 4 /Fe 2 O 3 hybrids were studied. Detail characterizations on charge transfer kinetics revealed that g-C 3 N 4 /nanodot-Fe 2 O 3 structure showed faster electron injection rate and higher injection efficiency (≈0.084 ns −1 and ≈27.5%) than g-C 3 N 4 /nanosheet-Fe 2 O 3 counterpart (≈0.054 ns −1 and ≈19.5%). Stronger intimate junction between g-C 3 N 4 nanosheets and Fe 2 O 3 nanodots was believed to be the reason for faster and more efficient electron injection. In addition, stronger interaction with tetracycline and higher reactivity with H 2 O 2 at the interface were observed for g-C 3 N 4 /nanodot-Fe 2 O 3 compared with g-C 3 N 4 /nanosheet-Fe 2 O 3 . Thereby, under visible light stimulation, g-C 3 N 4 /nanodot-Fe 2 O 3 demonstrated higher photo-Fenton-like tetracycline removal efficiency and rate (≈87% and ≈0.037 min −1 ) than g-C 3 N 4 /nanosheet-Fe 2 O 3 (≈57% and ≈0.016 min −1 ). Furthermore, g-C 3 N 4 /nanodot-Fe 2 O 3 junction can remain robust catalytic performance under various conditions (recycle experiment, real environment, different initial pHs and temperatures, anion coexistence, and other contaminants removal) and possible tetracycline degradation pathways were proposed. This study provided deep insights into structure-activity relationship and electron transfer between g-C 3 N 4 and nanostructured Fe 2 O 3 , which can open a new avenge to develop Fe 2 O 3 -based photo-Fenton catalysts with high efficiencies for antibiotic wastewaters remediation.
研究领域:
环境科学
·
材料科学
·
化学
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2021
·
IF 13.273
Rongdi Tang,Daoxin Gong,Yaocheng Deng,Sheng Xiong,Jie Deng,Ling Li,Zhanpeng Zhou,Jiangfu Zheng,Long Su,Lihua Yang
In this study, a novel π-π stacked PDI/g-C 3 N 4 /TiO 2 @Ti 3 C 2 photocatalyst with step-scheme (S-scheme) heterojunction was constructed to boost the atrazine (ATZ) photocatalytic degradation by activating peroxymonosulfate (PMS). The π-π interaction in the PDI/g-C 3 N 4 induced the delocalization of the photoelectrons, therefore promoted their migration. Meanwhile, the intimate contact and the staggered band configurations between the PDI/g-C 3 N 4 and TiO 2 @Ti 3 C 2 results in the S-scheme heterojunction thus declined the recombination of photocarriers. The π-π interaction and S-scheme heterojunction synergistically promoted the ATZ removal rate to 75% within one hour and can be well-adapted in a variety of environments. It was found that 1 O 2 domain the photocatalysis, and the H 2 O 2 generated during the reaction may also be helpful for the process. The transformation of ATZ, intermediates, and three pathways during the process were also investigated via LC-MS. Moreover, the total organic carbon analysis shows that the mineralization of ATZ reached 46.08%.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
Journal of Environmental Chemical Engineering
·
2025
·Vol. 14
·期 1
·120879
·
IF 7.2
Chengzhao Liu,Tao Liu,Suhua Liu,Xiufang Zhang,Guanlong Wang
Recently, it was reported photocatalytic H 2 O 2 generation performed in biphasic system could significantly increase the H 2 O 2 yield. Aiming to further improve the H 2 O 2 yield, hydrophobic heterojunction of α-S and vacancy-rich g-C 3 N 4 (CNN) was constructed. H 2 O 2 production performance tests demonstrated the 0.2α-S/CNN composite achieved H 2 O 2 yields 1.72 and 1.99 times higher than pristine CNN and α-S, respectively. N-(C) 3 bonded nitrogen(N 3 C ) promoted oxygen activation, and heterojunction facilitated the separation of photogenerated holes and electrons. These contributed more effective photocatalytic synthesis of H 2 O 2 . The optimal 0.2α-S/CNN achieved a production rate of 2218 μmol g −1 , with an impressive apparent quantum yield (AQE) of 6.92 % under 455 nm monochromatic light, outperforming the state-of-the-art catalysts. The proposed mechanism suggested that photogenerated electrons migrated from α-S to CNN, reducing adsorbed O 2 to form •O 2 − radicals. These radicals subsequently reacted with water in the aqueous phase to generate H 2 O 2 via 2e − ORR. Due to the strong hydrophobicity of the catalyst, most •O 2 − radicals were generated in benzyl alcohol (BA) phase, while H 2 O 2 predominantly formed in the aqueous phase. This spatial separation delayed H 2 O 2 decomposition, facilitating its accumulation and enhancing overall yield.
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2019
·Vol. 44
·期 31
·16348-16358
·
IF 4.084
Dandan Sun,Dechao Chi,Zekang Yang,Zipeng Xing,Junwei Yin,Zhenzi Li,Qi Zhu,Wei Zhou
Mesoporous g-C 3 N 4 /Zn–Ti layered double hydroxide (LDH)-laminated van der Waals heterojunction nanosheets were prepared by a facile one-step in situ hydrothermal method . Due to the strong electrostatic interactions between the positively charged Zn–Ti LDH and negatively charged g-C 3 N 4 nanocrystal , a laminated van der Waals heterostructure was successfully formed between Zn–Ti LDH and g-C 3 N 4 . The mesoporous g-C 3 N 4 /Zn–Ti LDH-laminated van der Waals heterojunction, which had a narrow bandgap of 2.41 eV extended the photoresponse to the visible light region. The obtained heterojunctions showed excellent visible-light-driven photocatalytic performance for the complete removal of ceftriaxone sodium (up to ∼97%) and a high hydrogen production rate (∼161.87 μmol h −1 g −1 ). This was mainly attributed to the formation of the laminated van der Waals heterojunctions, which favoured charge separation and the absorption of visible light, and the mesoporous structure, which provided more surface active sites. This facile strategy for preparing mesoporous g-C 3 N 4 /Zn–Ti LDH-laminated van der Waals heterojunctions offers new insights for the fabrication of high-performance van der Waals heterojunction photocatalytic materials.
研究领域:
材料科学
·
光催化
·
纳米材料
·
环境化学
·
能源化学
✓ 已验证
DOI
高影响因子
Desalination and Water Treatment
·
2024
·
IF 1
Xiang Li,Wei Li,Shiyu Xie,Guoming Zeng,Sarfaraz Khan
Despite low exposure level in the water, environmental hormone pollutants can still inflict significant biological effects that endanger ecological safety and human reproduction. However, they are unable to be effectively removed using ordinary water treatment methods, which makes the deposition of environmental residues highly likely. In light of this demand, this study synthesized metal-doped g-C 3 N 4 composite photocatalysts and coupled them with nitrogen doped ordered mesoporous (NMC) carbon to treat water contaminated by environmental hormone micropollutants. The experimental results show that AgIn 5 S 8 /g-C 3 N 4 (25%) makes the prime candidate for degrading bisphenol A (BPA), displaying the highest degradation rates of 82%. Moreover, h+ and·O 2− were found to be the main active substances in the photocatalytic process, while the degradation rate of BPA by AgIn 5 S 8 /g-C 3 N 4 (25%) was still over 80% after 5 repeated photocatalyses. When the nitrogen doped ordered mesoporous carbon was coupled with AgIn 5 S 8 /g-C 3 N 4 (25%), the degradation and removal rates of BPA were greatly improved, demonstrating up to 94.8% removal rate in batch treatment. Furthermore, NMC/AgIn 5 S 8 /g-C 3 N 4 also exhibited good adsorption–photocatalytic synergy under continuous flow conditions of the fluidized bed, and the highest removal rate of BPA in the dark-free adsorption experiment was about 98.1%.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2022
·
IF 5.518
Qihuang Deng,Jiangqiong Wang,Peiyao Chen,Maolin Bo,Ya’na Lu,Yuanfeng Pan,Hong Liu,Wanshan Duan,Jimin Xie,Yefeng Feng
Scattering medium-bandgap semiconductors into polymers cannot remarkably improve the dielectric constant in composites. Nanoscale ceramic leads to a high interface leakage current. To obtain a high dielectric constant and low loss, in this work, graphitic carbon nitride (g-C 3 N 4 )@PbS microparticles were prepared for fabricating polymer-based ternary composites. Polymer/PbS binary composites were also fabricated. In terms of electric properties, ternary composites show more advantages than binary composites. In ternary composites, the improved dielectric constant is ascribed to S N bonding at the g-C 3 N 4 /PbS interface. Decreased dielectric loss is rooted in the reduced interface leakage current (from the large size of the hybrid filler) between the polymer and PbS. Under high fields, the reduced breakdown strength is attributed to the reduced bandgap in the hybrid filler compared with PbS and g-C 3 N 4 . The innovation of this work is the high-efficiency collaboration between microsized and interfacial S N bonding in g-C 3 N 4 @PbS filler. The ternary composite with 15 wt% hybrid filler has a high dielectric constant of ~ 39 and a low dielectric loss of ~ 0.04 at 100 Hz (low field) as well as a high breakdown strength of ~ 202 MV m −1 under a direct-current field. This work might enlighten the fabrication of polymer composites with great promise in energy storage.
研究领域:
材料科学
·
电气工程
✓ 已验证
DOI
高影响因子
Polymers
·
2018
·Vol. 10
·期 11
·1264
·
IF 2.935
Jing Li,Meizhao Han,Yaseen Muhammad,Yu Liu,Zhibin Su,Jing Yang,Song Yang,Shaochan Duan
Styrene-butadiene styrene graphene oxide nanoplatelets (SBS-g-GOs)-modified asphalt was prepared by reacting thiolated GOs (GOs-SH) with SBS in asphalt using a thiol-ene click reaction. The temperature resistance and mechanical properties of asphalts were analyzed by dynamic shear rheology (DSR) and multiple-stress creep-recovery (MSCR) tests, which revealed that an optimum amount of GOs-SH (0.02%) can effectively improve the low temperature and anti-rutting performance of SBS asphalt. Segregation experiments showed that SBS-g-GOs possessed good stability and dispersion in base asphalt. Fluorescence microscopy results revealed that the addition of GOs-SH promoted the formation of SBS network structure. Textural and morphological characterization of GOs-SH and SBS were achieved by Fourier transform infra-red (FT-IR) spectroscopy, energy-dispersive X-ray spectroscopy (EDX), atomic-force microscopy (AFM), X-ray diffraction (XRD), and scanning electron microscopy (SEM), while surface chemical composition was tested by X-ray photoelectron spectroscopy (XPS). Based on textural characterization data, a suitable reaction mechanism was proposed that involved the preferential reaction between GOs-SH and 1,2 C=C of SBS. The currently designed GOs-SH incorporated asphalt via thiol-ene click reaction provides new ideas for the preparation of modified asphalt with enhanced mechanical properties for target-oriented applications.
研究领域:
材料科学
·
土木工程
✓ 已验证
DOI
高影响因子
RSC Advances
·
2019
·Vol. 9
·期 71
·41591-41602
·
IF 3.049
Yu Qiao,Qian Han,Dong Li,Hongji Li,Bing Wei,Guangbo Che,Wei Jiang,Weisheng Guan
A novel Ag/metal–organic framework/graphitic carbon nitride (Ag/HKUST-1/g-C3N4, AHC) photocatalyst was prepared via an in situ growth strategy and photo-deposition technique for environmental remediation. The as-obtained samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), N2 adsorption–desorption isotherm measurement, UV-vis diffuse reflection spectroscopy (UV-vis DRS), and photoluminescence (PL) spectroscopy. The results indicated that the hybrids have large surface area, mesoporous structure and enhanced visible-light absorption. The as-prepared hybrid samples exhibited considerable improvement in photocatalytic activity and stability for rhodamine B (RhB) degradation under visible light irradiation (λ > 420 nm). In addition, they also have good adsorption properties. Compared to the pure g-C3N4 and Ag/g-C3N4, the 5% AHC photocatalyst showed superior photocatalytic activity. Moreover, 5% AHC exhibits good photocatalytic activity even after four cycles. Additionally, the active species trapping and electron spin resonance (ESR) experiments indicated that h+ and ·OH were the main active species.
研究领域:
环境催化
·
材料化学
·
光化学
·
纳米材料
·
环境污染治理
✓ 已验证
DOI
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Jianfei Li,Bin Zhang,Junyan Lu,Zihao Guo,Mingxia Zhang,Degang Li,Zengdian Zhao,Shasha Song,Yan Liu,Luchang Qin
The path and mechanism of charge transfers in composite catalyst are important for degrading organic pollutants effectively. A quasi-ternary Z-scheme heterojunction photocatalyst with carbon quantum dots (CQD), CdS, and graphitic carbon nitride (g-C 3 N 4 ) (CQD/CdS/g-C 3 N 4 ) has been successfully constructed in this work, and its electron transfer path is elucidated by contrast CdS/CQD/g-C 3 N 4 photocatalyst. The built-in electric field at the interface between CdS and g-C 3 N 4 induces exciton separations. The energy barrier between CQD and CdS accelerated charge transfers and further prevents exciton annihilation. As a result, CQD/CdS/g-C 3 N 4 exhibits the greatest photocatalytic degradation, and the removal rates of Rhodamine B and sulfadiazine are 94.7 % and 76.0 %, which are 2.46 times and 1.47 times of CdS/CQD/g-C 3 N 4 , 7.02 times and 7.92 times of g-C 3 N 4 , respectively. It is further proved that CQD as the active site can promote the generation of H 2 O 2 and effectively inhibit the formation of •O 2 – in the photocatalytic reaction. In addition, the degradation pathway and products of sulfadiazine are explored by means of HPLC-MS and calculation of Gaussian software. This work demonstrates the relationship between photocatalytic activity and electron transfer path, meanwhile, provides a reference for the design of efficient heterogeneous photocatalysts for environmental remediation.
研究领域:
环境科学
·
材料科学
·
催化化学
✓ 已验证
DOI
高影响因子
危险品化学品经营许可证（带存储）