光催化
催化作用
材料科学
介孔材料
同种类的
金属
可见光谱
降级(电信)
吡啶
制氢
化学工程
纳米技术
化学
光电子学
有机化学
计算机科学
物理
冶金
工程类
电信
热力学
作者
Qin Su,Lei Yang,Jianfeng Huang,Limin Xiao,Jun‐Min Liu
标识
DOI:10.1002/asia.202100469
摘要
Abstract The design of photochemical molecular devices (PMDs) for photocatalytic H 2 production from water is a meaningful but challenging subject currently. Herein, a Pd 2 L 4 type metal‐organic cage (denoted as MOC‐Q2) is designed as a PMD, which consists of two catalytic centers (Pd 2+ ) and four photosensitive ligands (L‐2) with four pyridine anchoring groups. Subsequently, the MOC‐Q2 is combined with TiO 2 to form TiO 2 ‐MOC‐Q2 hybrid materials with different MOC‐Q2 contents by a facile sol‐gel method, which have micro/mesoporous structures and large surface areas. The optimized TiO 2 ‐MOC‐Q2 (6.5 wt%) exhibits high H 2 production activity (7.9 mmol g −1 h −1 within 5 h) and excellent durability, giving a TON value of 23477 or 11739 (based on MOC‐Q2 or Pd moles) after recycling for 7 rounds. By contrast, the pure MOC‐Q2 only shows an ordinary photocatalytic H 2 production rate (0.84 mmol g −1 h −1 within 5 h) in the homogeneous system. It can be deduced that TiO 2 drives the photocatalysis and simultaneously acts as the structure promoter. This study presents a meaningful and distinctive attempt of a new approach for the design and development of MOC‐based heterogeneous photocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI