Photoelectrochemical alcohols oxidation over polymeric carbon nitride photoanodes with simultaneous H2 production

被引:27
作者
Karjule, Neeta [1 ,2 ]
Phatake, Ravindra S. [1 ,2 ]
Barzilai, Shmuel [3 ]
Mondal, Biswajit [1 ,2 ]
Azoulay, Adi [1 ,2 ]
Shames, Alexander, I [4 ]
Volokh, Michael [1 ,2 ]
Albero, Josep [5 ]
Garcia, Hermenegildo [5 ]
Shalom, Menny [1 ,2 ]
机构
[1] Ben Gurion Univ Negev, Dept Chem, IL-8410501 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Ilse Katz Inst Nanoscale Sci & Technol, IL-8410501 Beer Sheva, Israel
[3] Nucl Res Ctr Negev, Dept Chem, POB 9001, IL-84910 Beer Sheva, Israel
[4] Ben Gurion Univ Negev, Dept Phys, IL-8410501 Beer Sheva, Israel
[5] Univ Politecn Valencia UPV, Inst Univ Tecnol Quim ITQ, CSIC, Avda Narajos S-N, Valencia 46022, Spain
基金
欧洲研究理事会; 以色列科学基金会;
关键词
SELECTIVE OXIDATION; BENZYL ALCOHOL; VISIBLE-LIGHT; G-C3N4; O-2; EFFICIENCY; CATALYSIS; ALDEHYDES;
D O I
10.1039/d2ta03660f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photoelectrochemical oxidation of organic molecules into valuable chemicals is a promising technology, but its development is hampered by the poor stability of photoanodic materials in aqueous solutions, low faradaic efficiency, low product selectivity, and a narrow working pH range. Here, we demonstrate the synthesis of value-added aldehydes and carboxylic acids with clean hydrogen (H-2) production in water using a photoelectrochemical cell based solely on polymeric carbon nitride (CN) as the photoanode. Isotope labeling measurements and DFT calculations reveal a preferential adsorption of benzyl alcohol and molecular oxygen to the CN layer, enabling fast proton abstraction and oxygen reduction, which leads to the synthesis of an aldehyde at the first step. Further oxidation affords the corresponding acid. The CN photoanode exhibits excellent stability (>40 h) and activity for the oxidation of a wide range of substituted benzyl alcohols with high yield, selectivity (up to 99%), and faradaic efficiency (>90%).
引用
收藏
页码:16585 / 16594
页数:10
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