Efficient solar light-driven H2 production: post-synthetic encapsulation of a Cu2O co-catalyst in a metal-organic framework (MOF) for boosting the effective charge carrier separation

被引:62
|
作者
Karthik, Peramaiah [1 ,2 ]
Balaraman, Ekambaram [3 ]
Neppolian, Bernaurdshaw [1 ,2 ]
机构
[1] SRM Univ, SRM Res Inst, Madras 603203, Tamil Nadu, India
[2] SRM Univ, Dept Chem, Madras 603203, Tamil Nadu, India
[3] CSIR NCL, Div Organ Chem, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
关键词
REDUCED GRAPHENE OXIDE; P-N HETEROJUNCTION; VISIBLE-LIGHT; PHOTOCATALYTIC ACTIVITY; HYDROGEN-PRODUCTION; POSTSYNTHETIC LIGAND; CR(VI) REDUCTION; HIGH-STABILITY; NANOPARTICLES; EXCHANGE;
D O I
10.1039/c8cy00604k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The development of new and efficient catalytic systems for solar light-driven hydrogen generation is one of the prime focuses of contemporary chemical sciences. Indeed, the charge carrier separation efficiency of a photocatalyst plays a vital role in photocatalysis. Herein, we have successfully designed a Cu2O-encapsulating NH2-MIL-125(Ti) MOF by a post-synthetic encapsulation strategy. The Cu2O-encapsulating MOF material showed a remarkable enhancement in photocatalytic H-2 production activity under solar light illumination. Gratifyingly, the H-2 production activity under solar light was around approximate to 28-fold higher than that of the pristine MOF. The enhancement in photocatalytic activity may be attributed to efficient charge carrier separation through Ti3+ sites and the broad light absorption of the Cu2O-encapsulating MOF photocatalyst. The possible electron transport mechanism, potential energy diagram (V vs. NHE), and the existence of Ti3+ ions have been demonstrated by various spectroscopic studies.
引用
收藏
页码:3286 / 3294
页数:9
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