Efficient photocatalytic hydrogen evolution over carbon supported antiperovskite cobalt zinc nitride

Photocatalytic solar to chemical energy conversion is an important energy conversion process but suffer from low efficiency. Thus, development of efficient photocatalytic system using earth-abundant elements with low costs is highly desirable. Here, antiperovskite cobalt zinc nitride has been synthesized and coupled with carbon black (Co3ZnN/C) for visible light driven hydrogen production in an Eosin Y-sensitized system. Replacement of cobalt atom by zinc atom leads to an improved charge transfer kinetics and catalytic properties compared with Co4N. Density functional theory (DFT) calculations further reveal the adjusted electronic structure of Co3ZnN by zinc atom introducing. The lower antibonding energy states of Co3ZnN are beneficial for the hydrogen desorption. Moreover, carbon black as support effectively reduces the particle size of Co3ZnN and benefits to the electron storage and adsorption capabilities. The optimal Co3ZnN/C catalysts exhibit the H-2 evolution rate of 15.4 mu mol mg(-1) h(-1),which is over 6 times higher than that of monometallic Co4N. It is even greater than those of most of Eosin Y-sensitized systems.

Automated summary

The development of efficient photocatalytic system using earth-abundant elements with low costs is highly desirable, and Co3ZnN coupled with carbon black has been synthesized for visible light driven hydrogen production. The replacement of cobalt atom by zinc atom leads to improved charge transfer kinetics and catalytic properties, while carbon black support effectively reduces particle size and enhances electron storage capabilities. The optimal Co3ZnN/C catalysts exhibit a H-2 evolution rate over 6 times higher than monometallic Co4N and outperform most Eosin Y-sensitized systems.