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

3 项

设置提升方向
光子转换
JOURNAL OF ALLOYS AND COMPOUNDS · 2025 · IF 6.3

Enhanced near-infrared photocatalytic activity of Bi3O4Br nanosheets via dual roles of rare earth ions doping: Photon conversion and energy band regulation

Zhifeng Li,Haowen Yan,Zhaoyi Yin,Guofeng Zhang,Yichao Wang,Sicheng Gao,Jie Pan,Zhiguo Song,Jianbei Qiu,Yongjin Li

The efficient utilization of near-infrared (NIR) light is an important challenge to extend the spectral response range of photocatalysts. Here, the NIR photocatalytic performance of Bi 3 O 4 Br nanosheets was significantly enhanced by a rare earth ion doping strategy that synergistically utilizes the dual mechanism of photon conversion and energy band modulation. Under 980 nm excitation, the Bi 3 O 4 Br:Er 3 + nanosheets exhibit near-single-band green upconversion (UC) emission and are reabsorbed by Bi 3 O 4 Br. Combined with DFT density of states calculations, it is shown that the band gap of the material has been lowered and the carrier transport paths have been optimized by the energy-band structural tuning. In the NIR photocatalytic degradation experiment of bisphenol A, Bi 3 O 4 Br was not degraded, and Bi 3 O 4 Br:Er 3+ showed better performance, which was 2.27 times higher than that of Bi 3 O 4 Br:Yb 3+ , Er 3+ . ESR testing and capture experiments indicate that under NIR light irradiation, •OH and e − are the primary active species in the photocatalytic reaction process. This work provides new design ideas for the development of efficient NIR photocatalytic materials.

研究领域: 材料科学 · 催化化学 · 纳米技术
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
Advanced Optical Materials · 2024 · IF 8

Tuning the 5d State of Pr3+ in Oxyhalides for Efficient Deep Ultraviolet Upconversion

Yangyang Du,Zhengyuan Jin,Ziyu Li,Tianying Sun,Haotian Meng,Xiaojuan Jiang,Yu Wang,Dengfeng Peng,Jianwei Li,Aiwu Wang,Hua Zou,Feng Rao,Feng Wang,Xian Chen

Visible-to-ultraviolet (UV) upconversion provides a fascinating strategy to achieve deep UV emission through readily accessible visible light. However, the intensity of deep UV emission obtained through visible-to-UV upconversion progress is still far from satisfactory, severely constraining its practical applications. Herein, a novel class of praseodymium ion (Pr 3+ )-doped rare-earth oxyhalides (YOCl, YOBr, and LuOBr) to achieve efficient upconverted deep UV emission in the spectral range of 250–350 nm is developed. The upconverted UV emission intensity of LuOBr:Pr 3+ is determined to be 56.7 times stronger than that of the well-established Lu 7 O 6 F 9 :Pr 3+ . When employed as a photon-converter to activate photocatalytic water splitting reactions, upconverted deep UV emission enables H 2 generation under visible light ( λ > 420 nm) excitation from a xenon lamp. The efficient deep UV upconversion stems from tuning 4 f 1 5 d 1 state of Pr 3+ by oxyhalide constituent which both facilitates the absorption of excitation photons in long-lived intermediate 4 f 2 states and suppress the probability of nonradiative relaxation from 4 f 1 5 d 1 state. These findings not only provide new insights into a mechanistic understanding of the host effect on upconversion process but also make a breakthrough in developing efficient deep upconversion materials that will expand their further applications.

研究领域: 材料科学 · 光子学 · 化学 · 光电
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ADVANCED MATERIALS · 2025 · IF 26.8

Intermediate-States Mediated 2D MoO3-x Plasmon Enabling Pure-Phased CsPbX3 Photovoltaics with 27.33% Bifacial Efficiency

Meng Cai,Wei Liu,Tiankai Zhang,Pengfei Yan,Yuxuan Li,Weiqian Kong,Hangjuan Wu,Zongwei Chen,Zhenkun Gu,Lin Dong,Qun Xu,Yanlin Song,Junjie Ma,Chongxin Shan,Feng Gao

All-inorganic CsPbX 3 (X = I, Br, Cl) perovskites emerged as a crucial material for addressing the stability bottleneck due to their exceptional resistance to both light-thermal stress. However, their performance is limited by adverse optoelectronic dissipation arising from inadequate photon conversion and chaotic carrier energetics. Herein, the mechanism of the unique nonlinear plasmonic effect in van der Waals 2D MoO 3-x is elucidated, which is mediated by electronic intermediate states. It demonstrates that the 2D MoO 3-x serves as a light-capture-antenna in heterodimensional CsPbX 3 -MoO 3-x optically coupled system, contributing to the accumulation the optical field energy on the nanoscale and resulting in a remarkable 59% increase in photon convergence. Additionally, facet-oriented carrier channels can be established through heteroepitaxy along matched Mo-O octahedron. This optoelectrical-bimodal-coupling engineering combined with a bifacial light-harvesting configuration yields a bifacial equivalent efficiency of 27.33%, which stands as the supreme performance in all-inorganic perovskite photovoltaics. Graphical This remarkable work combines supercritical CO 2 chemical engineering, two-dimension plasmon photophysical science, and perovskite photovoltaic technology. It introduces novel concepts like broad - spectrum coupled photon absorption, the intermediate - localized - states model, and optoelectrical - bimodal - coupling engineering. It aims to combat optoelectronic dissipation and enhance energy harvesting via a heterodimensional van der Waals optically coupled system.

研究领域: 光伏技术 · 等离激元学 · 纳米光子学 · 材料科学 · 光电子学 · 钙钛矿太阳能电池 · 固体物理学
✓ 已验证 产品关联 DOI PubMed 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。