光子
等离子体子
化学能
光电子学
吸收(声学)
量子效率
材料科学
太阳能
红外线的
碳氢化合物
人工光合作用
表面等离子体子
光化学
化学
催化作用
光学
物理
光催化
生物化学
有机化学
复合材料
生态学
生物
作者
Canyu Hu,Xing Chen,Jingxiang Low,Yaw‐Wen Yang,Hao Li,Di Wu,Shuangming Chen,Jianbo Jin,He Li,Huanxin Ju,Chia‐Hsin Wang,Zhou Lu,Ran Long,Li Song,Yujie Xiong
标识
DOI:10.1038/s41467-023-35860-2
摘要
Imitating the natural photosynthesis to synthesize hydrocarbon fuels represents a viable strategy for solar-to-chemical energy conversion, where utilizing low-energy photons, especially near-infrared photons, has been the ultimate yet challenging aim to further improving conversion efficiency. Plasmonic metals have proven their ability in absorbing low-energy photons, however, it remains an obstacle in effectively coupling this energy into reactant molecules. Here we report the broadband plasmon-induced CO2 reduction reaction with water, which achieves a CH4 production rate of 0.55 mmol g-1 h-1 with 100% selectivity to hydrocarbon products under 400 mW cm-2 full-spectrum light illumination and an apparent quantum efficiency of 0.38% at 800 nm illumination. We find that the enhanced local electric field plays an irreplaceable role in efficient multiphoton absorption and selective energy transfer for such an excellent light-driven catalytic performance. This work paves the way to the technique for low-energy photon utilization.
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