Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 38, Pages 25438-25443Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b07287
Keywords
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Funding
- Multi-Dimensional Directed Nanoscale Assembly Creative Research Initiative (CRI) Center of the National Research Foundation of Korea (MSIP) [2015R1A3A2033061]
- Asian Office of Airforce Research and Development program [AOARD FA 2386-14-1-4013]
- NRF - MEST [2014R1A2A1A09005656]
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Graphitic carbon nitride (g-C3N4) is a rising two-dimensional material possessing intrinsic semiconducting property with unique geometric configuration featuring superimposed heterocyclic sp2 carbon and nitrogen network, nonplanar layer chain structure, and alternating buckling. The inherent porous structure of heptazine-based g-C3N4 features electron-rich sp2 nitrogen, which can be exploited as a stable transition metal coordination site. Multiple metal-functionalized g-C3N4 systems have been reported for versatile applications, but local coordination as well as its electronic structure variation upon incoming metal species is not well understood. Here we present detailed bond coordination of divalent iron (Fe2+) through micropore sites of graphitic carbon nitride and provide both experimental and computational evidence supporting the aforementioned proposition. In addition, the utilization of electronic structure variation is demonstrated through comparative photocatalytic activities of pristine and Fe-g-C3N4.
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