材料科学
共价键
碳纳米管
催化作用
三碘化物
量子点
石墨氮化碳
纳米技术
化学工程
碳纤维
活动站点
堆积
有机化学
化学
物理化学
光催化
复合材料
电极
工程类
复合数
色素敏化染料
电解质
作者
Siyi Hou,Chang Yu,Xuedan Song,Yiwang Ding,Jiangwei Chang,Yingbin Liu,Lin Chen,Qianbing Wei,Xiubo Zhang,Jieshan Qiu
标识
DOI:10.1002/adfm.202212112
摘要
Abstract The catalytic performance of carbon nanotubes has still been hindered by the intrinsic and limited in‐plane electrocatalytic active sites, with a focus on improving their catalytic activity by covalent modifications, which require the relatively high energy input to dissociate the in‐plane atoms and create the active sites. Herein, an effective route is developed to modulate the in‐plane defective density and electronic structure of multi‐walled carbon nanotubes (MWCNTs) by ultra‐small‐sized g‐C 3 N 4 quantum dots (CNQDs) with abundant nitrogen species via π–π stacking. The non‐covalent bonded CNQDs on MWCNTs endow them with abundant catalytic active sites on the basal plane, still inheriting the intrinsic and fast electron‐transfer characteristics of MWCNTs. The optimized CNQDs/MWCNTs‐4 heterogeneous catalyst exhibits an optimal photoelectric conversion efficiency of up to 8.30% in probing reaction for triiodide reduction, outperforming the Pt reference (7.86%). The thermodynamic calculations further reveal that the CNQDs integrated on MWCNTs are capable of reducing the reaction energy barrier (Δ G ) of the rate‐determining step from I 2 to I − and adsorption state I * . The present study provides an efficient and non‐covalent strategy to construct excellent carbon‐based catalysts with abundant active sites, which is also enlightening for the preparation and application of other carbon‐based catalysts.
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