光催化
石墨氮化碳
材料科学
化学工程
热解
多孔性
产量(工程)
过氧化氢
制氢
碳纤维
催化作用
氮化物
电子转移
蒽醌
熔盐
分解水
能量转换效率
氮化碳
纳米技术
无机化学
多孔介质
盐(化学)
量子产额
作者
Jian Gao,Juan Zhang,Mingqing Zuo,Shufan Han,Jiaxian Wu,Yaping Chen,Zeyan Zhou,Xiaoping Zheng,Le Yu,Lei Han
出处
期刊:Small
[Wiley]
日期:2026-04-23
卷期号:22 (32): e73507-e73507
被引量:2
摘要
ABSTRACT Photocatalytic conversion of H 2 O and O 2 into H 2 O 2 provides a promising sustainable ambient–condition route alternative to energy–intensive anthraquinone processes for on–site H 2 O 2 production. Herein a series of K–doped cyano–rich g–C 3 N 4 with porous structure (g–PC 3 N 4 K) have been successful synthesized by a molten salt assisted pyrolysis with subsequent secondary pyrolysis under the assistance of sublimated sulfur. Experimental and theoretical results demonstrate that the synergistic effects of K─N electron channels and the introduction of ─C≡N as well as porous structure is beneficial to the exposure of catalytically activity sites and the rapid separation and transfer of photogenerated electron–hole pairs, which contributes to the improved photocatalytic performance for H 2 O 2 production. As expected, the optimal g–PC 3 N 4 K exhibits a 14.05–fold higher H 2 O 2 yield than pristine g–C 3 N 4 and high H 2 O 2 yield of 1625 µ M and high solar–to–chemical conversion (SCC) efficiency of 5.93% can be also achieved within one hour under sunlight illumination, indicating its excellent performance and potentially practical application for photocatalytic H 2 O 2 synthesis.
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