Key Laboratory of Advanced Materials and Devices for Post-Moore Chips, Ministry of Education, State Key Laboratory for Advanced Metals and Materials, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
Angew Chem Int Ed Engl. 2024 Nov 25;63(48):e202406527. doi: 10.1002/anie.202406527. Epub 2024 Oct 30.
Photosynthetic microorganisms, which rely on light-driven electron transfer, store solar energy in self-energy carriers and convert it into bioenergy. Although these microorganisms can operate light-induced charge separation with nearly 100 % quantum efficiency, their practical applications are inherently limited by the photosynthetic energy conversion efficiency. Artificial semiconductors can induce an electronic response to photoexcitation, providing additional excited electrons for natural photosynthesis to improve solar conversion efficiency. However, challenges remain in importing exogenous electrons across cell membranes. In this work, we have developed an engineered gold nanocluster/organic semiconductor heterostructure (AuNCs@OFTF) to couple the intracellular electron transport chain of living cyanobacteria. AuNCs@OFTF exhibits a prolonged excited state lifetime and effective charge separation. The internalized AuNCs@OFTF permits its photogenerated electrons to participate in the downstream of photosystem II and construct an oriented electronic highway, which enables a five-fold increase in photocurrent in living cyanobacteria. Moreover, the binding events of AuNCs@OFTF established an abiotic-biotic electronic interface at the thylakoid membrane to enhance electron flux and finally furnished nicotinamide adenine dinucleotide phosphate. Thus, AuNCs@OFTF can be exploited to spatiotemporally manipulate and enhance the solar conversion of living cyanobacteria in cells, providing an extended nanotechnology for re-engineering photosynthetic pathways.
光合微生物依赖于光驱动的电子转移,将太阳能储存在自我能量载体中,并将其转化为生物能。虽然这些微生物可以以近 100%的量子效率进行光诱导电荷分离,但它们的实际应用受到光合作用能量转换效率的固有限制。人工半导体可以对光激发产生电子响应,为天然光合作用提供额外的激发电子,从而提高太阳能转换效率。然而,在外源电子穿过细胞膜方面仍存在挑战。在这项工作中,我们开发了一种工程化的金纳米团簇/有机半导体杂化结构(AuNCs@OFTF),以偶联活蓝藻的细胞内电子传递链。AuNCs@OFTF 表现出延长的激发态寿命和有效的电荷分离。内化的 AuNCs@OFTF 允许其光生电子参与光系统 II 的下游,并构建定向的电子高速公路,从而使活蓝藻的光电流增加五倍。此外,AuNCs@OFTF 的结合事件在类囊体膜上建立了非生物-生物电子界面,以增强电子通量,并最终提供烟酰胺腺嘌呤二核苷酸磷酸。因此,AuNCs@OFTF 可用于在细胞内时空操纵和增强活蓝藻的太阳能转换,为重新设计光合作用途径提供了一种扩展的纳米技术。