光催化
异质结
半导体
材料科学
插层(化学)
溴化物
催化作用
三元运算
肺表面活性物质
纳米技术
化学工程
光化学
光电子学
化学
无机化学
有机化学
工程类
计算机科学
程序设计语言
作者
H Zhang,Tingting Si,Lan Yuan,Chuang Han,Yi‐Jun Xu
标识
DOI:10.1021/acsmaterialslett.4c02060
摘要
The scarcity of strategies to finely modulate the interface assembly between MXene and semiconductors often restricts their full potential for photocatalysis. Herein, resorting to the cetyltrimethylammonium bromide (CTAB) surfactant intercalation effect, we report the rational synthesis of hierarchical seaurchin-like CdS-Ti3C2Tx MXene-CTAB (CdS-T-C) ensembles to modulate the interface and structure of MXene-semiconductor heterojunctions for significantly boosted photoredox coupling catalysis. The ternary CdS-T-C exhibits markedly enhanced activity toward visible light photoreforming of benzyl alcohol (BA) to benzaldehyde (BAD) and H2 cooperatively, as compared to bare CdS and conventional CdS-Ti3C2Tx MXene (CdS-T) that suffer from serious MXene restacking with obvious electronic and optical property attenuation. Mechanistic studies reveal that the CTAB interfacial intercalation alleviates the restacking of Ti3C2Tx, thus weakening the light shielding effect while promoting the charge transport and surface activity of MXene. This work demonstrates an appealing strategy to regulate the interfacial cross-coupling configuration of MXene-semiconductor composites for efficient solar-to-chemical conversion.
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