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Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid SCIE
期刊论文 | 2025 , 64 (4) | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
WoS CC Cited Count: 1
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Abstract :

The construction of solar-to-chemical conversion system by mimicking the photosynthetic network of the chloroplast holds great promise on efficient solar energy utilization. We developed an artificial photosynthetic cell (APC) based on molecular biomimetic thylakoid (CoTPP-FePy) to split water into hydrogen and oxygen (H2 and O2) at low driving voltage (1.1 V) and neutral condition (pH approximate to 7). The CoTPP-FePy can emulate the light reaction in thylakoids to produce O2 by coupling light harvesting, photocatalysis, and electron/energy storage (FeIII/FeII-Py). Subsequently, a membrane electrode assembly (MEA) were employed to simulate the dark reaction, wherein the proton, electron and energy generated by the light reaction can drive the H2 producing process. By a temporally and spatially coupling of the light and dark reactions, the resulting APC achieved a solar conversion efficiency of 3.1 %, exceeding that of natural photosynthetic systems and demonstrating the potential of artificial photosynthesis.

Keyword :

Artificial photosynthesis Artificial photosynthesis Biomimetic chemistry Biomimetic chemistry Metal organic cage Metal organic cage Photocatalytic water oxidation Photocatalytic water oxidation Water splitting Water splitting

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GB/T 7714 Zhou, Enbo , Yan, Shichen , Zhang, Xiang et al. Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid [J]. | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2025 , 64 (4) .
MLA Zhou, Enbo et al. "Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid" . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION 64 . 4 (2025) .
APA Zhou, Enbo , Yan, Shichen , Zhang, Xiang , Baloch, Ateeq Ur Rehman , Hui, Yangdan , Wang, Futong et al. Artificial Photosynthetic Cell with Molecular Biomimetic Thylakoid . | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION , 2025 , 64 (4) .
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Fully Conjugated Biscarboxylate Self-Assembled Molecule Anchoring Enhances Conductive Oxide for Efficient Textured Perovskite/Silicon Tandem Solar Cells SCIE
期刊论文 | 2025 | ADVANCED FUNCTIONAL MATERIALS
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Abstract :

The solution-processible perovskite materials, utilizing the existing silicon infrastructure for perovskite/silicon tandem solar cells (P/S-TSCs), have attracted significant interest due to their low-cost and high efficiency. Hole-selective layers (HSLs) are essential for charge extraction and transport in P/S-TSCs. However, conventional HSLs often encounter issues such as poor conductivity, energy level mismatch, and incomplete coverage on textured surfaces. In this regard, a novel fully conjugated biscarboxylate-anchored self-assembled molecule with limited acidity, 5-(9H-dibenzo[a,c]carbazol-9-yl)-isophthalic acid (IPAPhCz), is developed to enhance interaction with the conductive oxide of ITO (Indium tin oxide), which forms a uniform and conformal coverage that significantly improves the crystalline quality of the top perovskite. Additionally, IPAPhCz features a large tilted dipole moment with optimized energy alignment for hole extraction. The resulting 1.68 eV single-junction PSC achieved a champion power conversion efficiency (PCE) of 22.78%, an increase of approximate to 10.37% over devices using 4PACz (PCE = 20.64%). Furthermore, textured P/S-TSCs based on IPAPhCz reached a champion PCE of 31.80% (approximate to 1 cm2), reflecting a approximate to 9.58% enhancement compared to that on 4PACz (PCE = 29.02%). Both devices incorporating IPAPhCz demonstrated improved stability. The findings present a significant methodology for the design of high-performance HSL materials for textured P/S-TSCs.

Keyword :

enhanced interaction on conductive oxide enhanced interaction on conductive oxide fully conjugated biscarboxylate self-assembled molecule fully conjugated biscarboxylate self-assembled molecule hole-selective layer hole-selective layer perovskite/silicon tandem solar cells perovskite/silicon tandem solar cells

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GB/T 7714 Yan, Tingxia , Zhou, Enbo , Li, Chi et al. Fully Conjugated Biscarboxylate Self-Assembled Molecule Anchoring Enhances Conductive Oxide for Efficient Textured Perovskite/Silicon Tandem Solar Cells [J]. | ADVANCED FUNCTIONAL MATERIALS , 2025 .
MLA Yan, Tingxia et al. "Fully Conjugated Biscarboxylate Self-Assembled Molecule Anchoring Enhances Conductive Oxide for Efficient Textured Perovskite/Silicon Tandem Solar Cells" . | ADVANCED FUNCTIONAL MATERIALS (2025) .
APA Yan, Tingxia , Zhou, Enbo , Li, Chi , Zhong, Yanyi , Zhang, Jiangbin , Han, Kai et al. Fully Conjugated Biscarboxylate Self-Assembled Molecule Anchoring Enhances Conductive Oxide for Efficient Textured Perovskite/Silicon Tandem Solar Cells . | ADVANCED FUNCTIONAL MATERIALS , 2025 .
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功能化给-受体型COFs及其太阳能转化性能的研究
会议论文 | 2025 , 127-128 | 第三届全国太阳能电池材料与器件发展研讨会
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Abstract :

太阳能到电化学能或高值化学品的高效转化是推进国家清洁能源战略实施的重要方案。然而,其能量转化效率仍受制于光生电荷复合与氧化还原反应动力学之间的失配问题。针对该关键瓶颈,提出功能化给-受体型共价有机框架(COFs)材料创新策略:一方面,通过构建二维电子给-受体结构与三维柱层传输网络,实现光生电荷的高效分离与维持长寿命电荷分离态;另一方面,筛选高效的氧化还原活性位点,构筑孔道内高效质荷传输网络,同步强化反应活性与迁移速率。

Keyword :

共价有机框架材料 共价有机框架材料 太阳能转化 太阳能转化 电荷分离 电荷分离 给-受体 给-受体

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GB/T 7714 周恩博 , 欧阳新华 . 功能化给-受体型COFs及其太阳能转化性能的研究 [C] //第三届全国太阳能电池材料与器件发展研讨会论文集 . 2025 : 127-128 .
MLA 周恩博 et al. "功能化给-受体型COFs及其太阳能转化性能的研究" 第三届全国太阳能电池材料与器件发展研讨会论文集 . (2025) : 127-128 .
APA 周恩博 , 欧阳新华 . 功能化给-受体型COFs及其太阳能转化性能的研究 第三届全国太阳能电池材料与器件发展研讨会论文集 . (2025) : 127-128 .
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Electronically Modulated TpPa COF as a High-Performance Iodine Host for Zn-I2 Batteries SCIE
期刊论文 | 2025 | SMALL
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Abstract :

The practical application of aqueous zinc-iodine (Zn-I2) batteries is hindered by poor iodine utilization and limited cycling stability, primarily due to the shuttle effect of soluble polyiodide species. In this study, side-group engineering is employed to modulate the electronic structure of hexagonal porous TpPa covalent organic frameworks (COFs). Among the engineered COFs, the nitro-functionalized TpPa COF (TpPa-NO2) outperforms in both I2 utilization and cycling stability, achieving a high specific capacity of approximate to 183 mAh g-1 at 0.1 A g-1 and a remarkable capacity retention of 84.3% after 10 000 cycles at 5 A g-1. Notably, the TpPa-NO2-based Zn-I2 batteries maintain mitigated polarization and stable operation under harsh conditions, including low temperatures (-5 degrees C) and high iodine loading (approximate to 15 mg cm-2). Theoretical simulations reveal that the electronic modulation reduces the TpPa COF's band gap and enhances the affinity for polyiodide species, thus improving the I2 utilization. These findings are further supported by in situ Raman and UV-vis spectroscopy, which identified a dominant I-/I5 - redox pathway and confirmed suppression of polyiodide dissolution. This work underscores the promise of electronically tailored COFs as advanced cathode hosts for long-life Zn-I2 batteries, offering an effective dual strategy to enhance iodine utilization and mitigate the shuttle effect.

Keyword :

covalent organic framework covalent organic framework electronic modulation electronic modulation low-temperature low-temperature nitro group nitro group zinc-iodine battery zinc-iodine battery

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GB/T 7714 Sun, Yunlong , Shao, Qiwang , Wang, Shuangshou et al. Electronically Modulated TpPa COF as a High-Performance Iodine Host for Zn-I2 Batteries [J]. | SMALL , 2025 .
MLA Sun, Yunlong et al. "Electronically Modulated TpPa COF as a High-Performance Iodine Host for Zn-I2 Batteries" . | SMALL (2025) .
APA Sun, Yunlong , Shao, Qiwang , Wang, Shuangshou , Yu, Yinghua , Xu, Jie , Zhou, Enbo et al. Electronically Modulated TpPa COF as a High-Performance Iodine Host for Zn-I2 Batteries . | SMALL , 2025 .
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