Journal
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 11, Issue 20, Pages 8873-8879Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c02756
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Funding
- U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-FG02-07ER15909]
- National Science Foundation [1954453]
- DOE Office of Science [DE-SC0012704]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [1954453] Funding Source: National Science Foundation
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Graphitic carbon nitride (g-C3N4) and its doped analogues have been studied over the past decade in part due to their promising applications in heterogeneous photocatalysis; however, the effect of doping on the photoconductivity is poorly understood. Herein, we investigate Cu doped g-g-C3N4 (Cu-g-C3N4) and demonstrate via extended X-ray absorption fine structure that Cu+ incorporates as an individual ion. Time-resolved optical pump terahertz probe spectroscopy was utilized to measure the ultrafast photoconductivity in response to a 400 nm pump pulse and showed that the Cu+ dopant significantly enhances photoconductivity of the as-prepared powdered sample, which decays within 10 ps. Furthermore, a film preparation technique was applied that further enhanced the photoconductivity and induced a longer-lived photoconductive state with a lifetime on the order of 100 ps. This study provides valuable insight into the ultrafast photoconductivity dynamics of g-g-C3N4 materials, which is essential toward developing efficient g-g-C3N4 photocatalysts.
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