Z-Scheme nanocomposite with high redox ability for efficient cleavage of lignin C–C bonds under simulated solar light. Issue 24 (25th November 2021)

• Record Type: Journal Article
• Authors: Wu, Xuejiao; Lin, Jinchi; Zhang, Huizhen; Xie, Shunji; Zhang, Qinghong; Sels, Bert F.; Wang, Ye
• Is Part Of: Green chemistry. Volume 23:Issue 24(2021)
• Page Start: 10071
• Page End: 10078
• Publication Date: 2021-11-25
• Subjects: Environmental chemistry -- Industrial applications -- Periodicals; Environmental management -- Periodicals; 660
• DOI: 10.1039/d1gc03455c
• Languages: English
• ISSNs: 1463-9262

Abstract

Abstract : Ag3 PO4 –PCN nanocomposite effectively cleaves C–C bonds of β-1 lignin models under simulated solar light mainly through an electron–hole coupled mechanism. The strong redox capability of the Z-scheme photocatalyst is the key to high efficiency. Abstract : Depolymerization of lignin, a key component of lignocellulose, is a sustainable approach to provide value-added aromatics. Selective cleavage of recalcitrant C–C linkages is a key challenge for lignin depolymerization. Photocatalysis, which can provide highly reactive species under mild conditions, represents a potential strategy for such C–C bond cleavage. Here, we report an efficient approach to break lignin C–C bonds using a Z-scheme Ag3 PO4 −polymeric carbon nitride (PCN) nanocomposite under simulated solar light at room temperature. Various lignin model compounds were converted into aromatic aldehydes with high yields of 66%–95%. Our mechanistic study reveals that the C–C bond cleavage mainly involves an electron–hole coupled photoredox mechanism. The construction of a Z-scheme Ag3 PO4 –PCN heterojunction structure is essential to simultaneously preserve the strong reduction and oxidation capability of its components, which is key for the electron–hole coupled Cα –Cβ bond cleavage. The present work offers useful guidance for the design of efficient semiconductors for C–C bond cleavage through band structure engineering.