解聚
木质素
光催化
材料科学
碱度
碳纤维
化学工程
氮气
格式化
氮化碳
氮化物
离子液体
太阳能燃料
离子键合
降级(电信)
甲酸甲酯
苯甲醛
石墨氮化碳
纳米技术
分子工程
带隙
载流子
光化学
有机化学
水解
可见光谱
无机化学
化学
聚合物
作者
Jiyuan Xu,Rongrong Zhao,Xuele Geng,Yiyi Sun,Qingyan Chu,Feng Song,Yujiao Xie,Jian‐Ping Zou,Zhe‐Ning Chen,Hongyou Cui,Hongzi Tan
标识
DOI:10.1021/acs.jafc.6c05057
摘要
The urgent necessity for sustainable lignin valorization drives the development of photocatalytic depolymerization. This study introduces an alkali-mediated strategy to engineer intralayer nitrogen defects and interlayer spacing in carbon nitride. KOH-synthesized g-C3Nx (K-C3Nx) delivers the best performance due to balanced alkalinity and ionic radius. Comprehensive characterizations confirm that KOH generates abundant nitrogen defects and expanded interlayer spacing, synergistically narrowing the band gap and suppressing carrier recombination. These advantages endow K-C3Nx with prolonged carrier lifetime and efficient visible light harvesting, achieving 64.0% conversion of 2-phenoxy-1-phenylethanol to benzaldehyde (51.2%) and phenyl formate (34.8%) via Cα-Cβ cleavage. K-C3Nx also enables selective scission of Cα-Cβ in various lignin model compounds and extracted methanosolv lignin. Mechanistic studies reveal that photogenerated electrons reduce O2 to •O2-, which combine with H+ and •Cβ to form a six-membered transition state, facilitating Cα-Cβ cleavage. This work establishes a dual-parameter engineering approach for synthesizing carbon nitride, enabling sustainable lignin depolymerization into aromatic monomers.
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