Selective cleavage of C-C linkages is the key and a challenge for lignin degradation to harvest value-added aromatic compounds. To this end, electrocatalytic oxidation presents a promising technique by virtue of mild reaction conditions and strong sustainability. However, the existing electrocatalysts (traditional bulk metal and metal oxides) for C-C bond oxidative cleavage suffer from poor selectivity and low product yields. We show for the first time that atomically dispersed Pt-NC sites planted on nitrogen-doped carbon nanotubes (Pt/N-CNTs), constructed via a stepwise polymerization-carbonization-electrostatic adsorption strategy, are highly active and selective toward C-C bond cleavage in β-O-4 model compounds under ambient conditions. Pt/N-CNTs exhibits 99% substrate conversion with 81% yield of benzaldehyde, which is exceptional and unprecedented compared with previously reported electrocatalysts. Moreover, Pt/N-CNTs using only 0.41 wt % Pt achieved a much higher benzaldehyde yield than those of the state-of-the-art bulk Pt electrode (100 wt % Pt) and commercial Pt/C catalyst (20 wt % Pt). Systematic experimental investigation together with density functional theory (DFT) calculation suggests that the superior performance of Pt/N-CNTs arises from the atomically dispersed Pt-NC sites facilitating the formation of a key C radical intermediate, further inducing a radical/radical cross-coupling path to break the C-C bond. This work opens up opportunities in lignin valorization via a green and sustainable electrochemical route with ultralow noble metal usage.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jacs.1c02328DOI Listing

Publication Analysis

Top Keywords

c-c bond
16
atomically dispersed
12
dispersed pt-nc
12
pt-nc sites
12
bond cleavage
8
ambient conditions
8
c-c
5
sites enabling
4
enabling efficient
4
efficient selective
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!