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中国物理学会期刊

紫精金属配合物Co(BPYBDC)(H2O)5∙(BDC)∙H2O的高压结构稳定性和光电性能

CSTR:32037.14.aps.75.20251347

High-pressure structural stability and photoelectric properties of viologen metal complex Co(BPYBDC)(H2O)5∙(BDC)∙H2O

CSTR:32037.14.aps.75.20251347
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  • 光探测器在光通信、环境监测和医学成像等领域具有重要应用, 其性能与核心材料的性质密切相关, 因此高性能光探测材料的研究一直是材料研究领域的热点和前沿方向. 紫精有机材料因其独特的氧化还原与变色特性, 在电致变色器件、生物传感器件及液流电池等方面得到广泛应用. 本工作设计并合成了含过渡金属元素Co的紫精配合物 Co(BPYBDC)(H2O)5·(BDC)·H2O (简称 1-Co), 利用一系列原位高压下的测试技术对 1-Co 开展了系统研究. 研究结果表明, 1-Co具有 Pc 晶体结构, 随着压强升至11.6 GPa, 其晶体结构保持稳定, 未发生结构相变. 紫外-可见吸收光谱显示, 升压过程中其吸收边红移, 样品颜色发生由无色透明向黄色的转变, 其高压下的输运和光电性能研究结果显示, 压强提高了电荷传输能力, 但显著削弱了光电流响应度. 研究揭示了高压下分子轨道重叠增加, 带隙降低, 分子间距离缩短, 使样品更容易形成电荷转移通道, 促进了紫精自由基的生成, 但紫精自由基的产生抑制了光电流的分离和传输过程. 本研究获得了1-Co在高压下的结构-性能关系, 为紫精基光电功能材料的应用提供了重要依据.

    Photodetectors play an essential role in optical communications, environmental monitoring, and medical imaging, and their performance strongly depends on the properties of the optoelectronic materials. Therefore, the exploration of high-performance optoelectronic materials has long been a research focus in the field of materials science. Viologen-based organic materials, owing to their unique redox and chromic characteristics, have been extensively utilized in electrochromic devices, biosensors, and flow batteries. In this work, a viologen complex containing the transition metal element Co, Co(BPYBDC) (H2O)5∙(BDC)∙H2O (denoted as 1-Co) is designed and synthesized. A series of in situ high-pressure characterization techniques is used to systematically investigate its structural and optoelectronic behaviors. The results reveal that 1-Co crystallizes in the Pc space group and remains structurally stable up to 11.6 GPa without any phase transition. UV-vis absorption spectroscopy shows a red-shift of the absorption edge upon compression, accompanied by a color change from colorless to yellow, indicating a pressure-induced narrowing of the optical bandgap. Consistent with the bandgap narrowing, impedance measurements show a significant decrease in total resistance under compression, which remains about two orders of magnitude lower than the initial value after decompression. Furthermore, the photocurrent response is markedly suppressed under compression and shows negligible recovery upon pressure release. This behavior can be attributed to the enhanced recombination of electrons with viologen groups under compression, leading to the formation of stable viologen radical states. These localized radicals cannot effectively participate in the separation and transport of photogenerated carriers, thereby contributing little to the photocurrent. These findings suggest that high pressure effectively modulates the optical and electrical behaviors of 1-Co by adjusting intermolecular interactions and the electronic band structure, thereby providing valuable insights into the pressure-dependent behavior of viologen-based materials.

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