Computational screening of MN (M = Ti-Cu) based metal organic frameworks for CO reduction using the d-band centre as a descriptor

• Published in: Nanoscale 2020-03, Vol.12 (1), p.6188-6194
• Main Authors: Mao, Xin, Tang, Cheng, He, Tianwei, Wijethunge, Dimuthu, Yan, Cheng, Zhu, Zhonghua, Du, Aijun
• Format: Article
• Language: English
• ISSN: 2040-3364; 2040-3372
• DOI: 10.1039/c9nr09529b

Electrocatalytic reduction is considered to be a promising way for the green and sustainable conversion of CO 2 into fuels and chemicals. Transition metals, copper particularly, are the most popular catalysts for this process and a wide range of reduced carbon compounds can be obtained. In previous studies, the binding energies of *CO and *OH were adopted as descriptors to screen out the best catalyst. However, this approach is not effective for those catalysts that have a weak interaction with CO molecules. Herein, we present a theoretical work by using the d-band centre as a descriptor to predict the best catalyst for CO 2 reduction to CH 4 based on newly synthesized metal organic frameworks, namely porous M 3 (HITP) 2 (HITP, 2,3,6,7,10,11-hexaiminotriphenylene) two-dimensional metal organic frameworks (MN 4 -MOFs). The limiting potentials of MN 4 -MOFs (M = Ti to Cu) for CO 2 reduction, determined by the formation energy of *OCHOH and *OCH 2 OH species, are closely correlated with the d-band centre from the TiN 4 -MOF to CuN 4 -MOF. Among the eight catalysts examined, the FeN 4 -MOF turns out to be the most active one for the selective conversion of CO 2 to CH 4 with an ultralow limiting potential of only −0.41 V, which is comparable or even lower than that of other reported CO 2 reduction catalysts. Designing a new synthesized MOF for CO 2 reduction based on d band center.