过电位
光电流
异质结
电催化剂
催化作用
还原(数学)
氧化还原
材料科学
退火(玻璃)
复合材料
纳米技术
选择性
化学工程
光电子学
化学
物理化学
数学
工程类
几何学
电化学
电极
生物化学
冶金
作者
Erhui Zhang,Jing Tang,Zirong Li,Yongsheng Zhou
标识
DOI:10.1002/celc.202200134
摘要
A novel method for constructing a g-C3N4/SnO2 heterostructure for CO2 reduction reaction (CO2RR) is presented. In the heterostructure, the introduction of g-C3N4 makes for restraining the recombination of photo-induced electrons and holes while the existence of SnO2 plays a vital role in selective catalytic reduction of CO2 into HCOOH, thus their cooperative interaction makes the photoelectric property of g-C3N4/SnO2 towards CO2RR improved greatly. The so-fabricated g-C3N4/SnO2 shows an exclusive HCOOH selectivity and a high faradic efficiency of 58 %, which is about 8 times higher than that of single SnO2. The photocurrent reaches 7.5 μA cm−2 under 0.5 V. Besides, the overpotential is as low as 300 mV (vs. RHE). Moreover, the PL emission decreases obviously after the introduction of g-C3N4. Given these performance advantages of g-C3N4/SnO2, the solution-processed strategy with post-annealing treatment offers a facile, efficient, yet scalable approach reference to construct CO2RR heterostructure catalysts, which shows higher potential in CO2RR electrocatalysis.
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