材料科学
氮化碳
光催化
聚合
化学工程
过氧化氢
碳纤维
氮化物
兴奋剂
氢
氧气
载流子
纳米技术
化学气相沉积
石墨氮化碳
冷凝
制氢
析氧
缩合反应
分解水
光化学
降级(电信)
反应条件
聚合物
催化作用
作者
Devesh Garg,Gabriel Mark,Venugopala Rao Battula,Yotam Engel,Rohit Kumar Saini,Alexander I. Shames,Thamaraichelvan Marichelvam,Daniel A. Grave,Michael Volokh,Menny Shalom
出处
期刊:Small
[Wiley]
日期:2026-01-17
卷期号:22 (14): e13234-e13234
被引量:1
标识
DOI:10.1002/smll.202513234
摘要
Potassium-ion (K+)-doped polymeric carbon nitride (CN) photocatalyst panels (PCPs) with cyano group defects stand out as an easy, low-cost, and scalable strategy for solar-driven chemical transformations, particularly for hydrogen peroxide (H2O2) production via the oxygen reduction reaction (ORR). However, due to the challenges inherent to the synthetic routes, it is almost impossible to grow alkali-metal-doped CN directly on substrates as panels. Here, we introduce a scalable and straightforward vapor-phase condensation and polymerization of CN precursors over KCl-coated substrates, achieving K+ doping and forming stable layers with enhanced light absorption, which results in the successful formation of charge carriers below the undoped CN's band edge. The optimal PCPs exhibit improved H2O2 production, particularly in 100% ethanol, reaching (3.0 ± 0.4) × 102 mM m-2 h-1, ∼18 times higher than control undoped CN PCPs (17 ± 4 mM m-2 h-1) in batch mode. The optimized PCP was evaluated as a large-scale panel (ca. 46 cm2) in a continuous-flow configuration for 96 h, yielding ∼39 mM m- 2 h-1 H2O2 during the first 24 h and demonstrating this configuration's scalability.
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