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银修饰石墨相氮化碳中的超快电荷注入。

Ultrafast Charge Injection in Silver-Modified Graphitic Carbon Nitride.

机构信息

Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana 59717, United States.

Montana Tech Nanotechnology Laboratory, Montana Technological University, Butte, Montana 59701, United States.

出版信息

ACS Appl Mater Interfaces. 2023 Mar 29;15(12):15478-15485. doi: 10.1021/acsami.2c22870. Epub 2023 Mar 16.

Abstract

Graphitic carbon nitride (gCN) is a promising organic platform for driving light-activated charge-transfer reactions in a number of valuable photocatalytic cycles. A primary limitation of gCN as a photocatalyst is its short excited-state lifetime, which is mediated by a high density of trap and defect sites that result in rapid excited-state decay and low photocatalytic efficiency. To enhance the catalytic activity, gCN is often functionalized with a metal co-catalyst; however, the mechanism by which metal co-catalysts enhance the reactivity has not been clearly established. In this work, the excited-state dynamics of gCN and silver-modified gCN are compared using ultrafast transient absorption and time-resolved photoluminescence spectroscopies. In silver-modified gCN, an ultrafast spectral shift in the silver plasmon resonance provides direct spectral evidence of electron transfer from gCN to the silver nanoparticles. The electron-transfer rate is competitive with other non-radiative relaxation pathways, with electron-transfer yields approaching 50%, thus providing an effective strategy for mitigating losses associated with defects and trap sites.

摘要

石墨相氮化碳(gCN)是一种很有前途的有机平台,可以在许多有价值的光催化循环中驱动光激活的电荷转移反应。gCN 作为光催化剂的一个主要局限性是其激发态寿命短,这是由高密度的陷阱和缺陷位引起的,导致快速的激发态衰减和低的光催化效率。为了提高催化活性,gCN 通常用金属助催化剂进行功能化;然而,金属助催化剂增强反应性的机制尚未明确建立。在这项工作中,使用超快瞬态吸收和时间分辨光致发光光谱比较了 gCN 和银修饰 gCN 的激发态动力学。在银修饰的 gCN 中,银等离子体共振的超快光谱位移提供了 gCN 向银纳米粒子电子转移的直接光谱证据。电子转移速率与其他非辐射弛豫途径竞争,电子转移产率接近 50%,从而为减轻与缺陷和陷阱位相关的损耗提供了一种有效的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/220d/10064998/fe0c901a93b7/am2c22870_0002.jpg

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