光电阴极
石墨烯
催化作用
光电流
材料科学
化学工程
阴极
电子转移
硅
光化学
纳米技术
化学
光电子学
有机化学
物理
物理化学
量子力学
工程类
电子
作者
Zhihe Wei,Yanhui Su,Weiyi Pan,Junxia Shen,Ronglei Fan,Wenjun Yang,Zhao Deng,Mingrong Shen,Yang Peng
标识
DOI:10.1002/anie.202305558
摘要
Abstract Silicon semiconductor functionalized with molecular catalysts emerges as a promising cathode for photoelectrochemical (PEC) CO 2 reduction reaction (CO 2 RR). However, the limited kinetics and stabilities remains a major hurdle for the development of such composites. We herein report an assembling strategy of silicon photocathodes via chemically grafting a conductive graphene layer onto the surface of n + ‐p Si followed by catalyst immobilization. The covalently‐linked graphene layer effectively enhances the photogenerated carriers transfer between the cathode and the reduction catalyst, and improves the operating stability of the electrode. Strikingly, we demonstrate that altering the stacking configuration of the immobilized cobalt tetraphenylporphyrin (CoTPP) catalyst through calcination can further enhance the electron transfer rate and the PEC performance. At the end, the graphene‐coated Si cathode immobilized with CoTPP catalyst managed to sustain a stable 1‐Sun photocurrent of −1.65 mA cm −2 over 16 h for CO production in water at a near neutral potential of −0.1 V vs. reversible hydrogen electrode. This represents a remarkable improvement of PEC CO 2 RR performance in contrast to the reported photocathodes functionalized with molecular catalysts.
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