文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,364+ SCI 论文 与阿拉丁产品引用相关
2,295,288.15 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

热门产品

视图 列表 网格

4 项

设置提升方向
P掺杂g-C3N4
MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2024 · IF 4.2

0D/2D Ti3+-TiO2/P-doped g-C3N4 S-scheme heterojunctions for efficient photocatalytic H2 evolution

Min Yuan,Ke Huang,Dongqing Dai,Hongfei Yin,Wei Zhao,Yixin Jiang,Yahui Feng

The integration of heterogeneous photocatalysts has emerged as a promising approach to boost the effectiveness of photocatalytic reactions for hydrogen evolution. In this study, we explore the synergistic effects of Ti 3+ -TiO 2 /P-doped g-C 3 N 4 heterojunctions on the enhancement of visible light-induced hydrogen generation efficiency. The photocatalytic hydrogen evolution performance of the as-prepared TPCN100 (280.38 μmol g −1  h −1 ) surpasses that of pristine P-doped g-C 3 N 4 (34.89 μmol g −1  h −1 ) and Ti 3+ -TiO 2 (39.71 μmol g −1  h −1 ) by factors of 8.0 and 7.1 respectively. Through a comprehensive investigation of the structural, electronic, and photocatalytic properties, the underlying mechanisms accountable for the observed enhancement in efficiency within the heterojunction system were elucidated. Based on the in-situ X-ray photoelectron spectrometer (XPS) examination, measurement of band edge, and electron paramagnetic resonance (EPR) analysis, the S-scheme photocatalytic mechanism was proposed. The integration of Ti 3+ -TiO 2 and P-doped g-C 3 N 4 offers new insights into the design of advanced photocatalytic materials for sustainable energy applications.

CAS / MDL: 108-78-1 102-71-6
研究领域: 材料科学 · 能源化学 · 环境科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Synergistically enhanced photocatalytic degradation of tetracycline hydrochloride by Z-scheme heterojunction MT-BiVO4 microsphere/P-doped g-C3N4 nanosheet composite

Xudong Yin,Xiaojie Sun,Yufeng Mao,Ruzhen Wang,Dehao Li,Wenyu Xie,Zhenghui Liu,Zhisen Liu

The elimination of tetracycline hydrochloride (TC-HCl) from water has attracted extensive research attention. This study hydrothermally synthesized composite photocatalysts composed of BiVO 4 microspheres containing coexisting phases of monoclinic scheelite (M-BiVO 4 ) and tetragonal zircon (T-BiVO 4 ), i.e., MT-BiVO 4 , loaded onto P-doped g-C 3 N 4 nanosheets (PCNS). Furthermore, their morphology, structure, and photoelectrochemical properties were comprehensively characterized, and the performance and stability of photocatalytic degradation of TC-HCl were examined. Additionally, the effects of humic acid (HA), coexisting anions/cations, and actual water samples on the degradation efficiency of TC-HCl were investigated, and the degradation mechanism and pathways were examined. The findings indicated that the percentage of M-BiVO 4 in MT-BiVO 4 considerably influences the photocatalytic activity of the composite catalyst. Furthermore, the excellent photocatalytic performance of 5% BVO/PCNS was attributed to the synergistic effects of P-doping the modified g-C 3 N 4 , MT-BiVO 4 isotype heterojunction effects, and the Z-scheme heterojunction constructed from MT-BiVO 4 and PCNS, which can enhance the absorption range of the visible light and accelerate the transfer and separation of charge carriers between catalysts. The free radical capture experiments and electron spin resonance tests indicated that holes and O 2 - were the dominant active species in the photocatalytic degradation process. With high reusability and stability, the 5% BVO/PCNS composite has great potential for practical wastewater treatment applications. This study offers a new approach for preparing photocatalysts synergized by isotype and Z-scheme heterojunctions.

CAS / MDL: 7803-55-6 64-75-5
研究领域: 环境科学 · 材料科学
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Journal of Materials Chemistry A · 2020 ·Vol. 8 ·期 43 ·22720-22727 · IF 11.301

Efficient visible-light activation of molecular oxygen to produce hydrogen peroxide using P doped g-C3N4 hollow spheres

Xueming Dang,Ruying Yang,Zhe Wang,Siyi Wu,Huimin Zhao

Graphitic carbon nitride (g-C3N4) possesses unique electronic and optical properties in the visible-light-driven production of H2O2. However, bulk g-C3N4 suffers from inefficient sunlight absorption and low carrier mobility. Herein, P doped g-C3N4 with a hollow sphere architecture was synthesized. The hollow sphere structure provides a large accessible surface area for charge transfer and enhances photo-absorption properties. Particularly, the doped P can regulate the energy band structure with stronger reducibility for O2 activation and accelerate photo-generated carrier separation. Meanwhile, the P heteroatom is beneficial to produce 1,4-endoperoxide species more easily and enhance selectivity for H2O2 synthesis through a two-electron O2 reduction process. The resultant catalyst exhibits a high H2O2 production rate of 174 μmol h−1 g−1 in pure water and 1684 μmol h−1 g−1 with isopropanol as a hole scavenger, which are 7.5 and 11.2 times those of bulk g-C3N4. This work provides a new avenue for the design and modification of other photocatalysts for H2O2 production.

研究领域: 材料科学 · 光化学 · 催化
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ChemistrySelect · 2025 ·Vol. 10 ·期 30 ·e01615 · IF 2

In-Situ Construction of P-Doped G-C3N4/Ag3PO4 Z-Scheme Heterojunctions with Broad pH Adaptability in Combination with Persulfate for Ultra-Efficient Photocatalytic Degradation of RhB

Bing Wang,Pinliang Lai,Jian Zhang,Guomin Li,Rao Fu,Hui Liu

Graphical The AgPCN+APS photocatalytic system was constructed in situ and its performance in degrading dyes in complex water environments was systematically investigated. It is of vital importance to develop highly efficient photocatalysts capable of removing dyes from actual wastewater environments. In this study, we constructed a in-situ, novel P-doped g-C 3 N 4 /Ag 3 PO 4 Z-scheme heterojunction photocatalyst (AgPCN) to degrade rhodamine B(RhB) in wastewater activated by persulfate (APS). Without the addition of persulfate, the kinetic degradation constant of RhB degraded by AgPCN can reach 0.53619 min −1 . Under the activation with a specific amount of persulfate, the kinetic degradation constant of RhB in the AgPCN + APS photocatalytic system can reach 0.78844 min −1 , which is 1.47 times higher than that of pure AgPCN. This is attributed to the structural defects of AgPCN itself and the energy level transformation caused by doping. Additionally, the activation of APS stimulates the generation of free radicals such as SO 4 · 2− , O 2 · − , and ·OH during the degradation process of AgPCN. It is worth noting that the AgPCN + APS system has a wide pH tolerance, indicating its application potential in complex actual wastewater environments. After three cycles of experiments, it still maintained a degradation efficiency of over 95%. Therefore, the AgPCN + APS system features excellent stability and wide applicability, providing a promising technical approach for the industrial treatment of dye wastewater.

研究领域: 环境科学 · 材料科学 · 化学工程 · 光催化 · 水处理技术
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。