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将石墨烯共价接枝到硅光阴极上以加速水相光电化学 CO 还原。

Covalently Grafting Graphene onto Si Photocathode to Expedite Aqueous Photoelectrochemical CO Reduction.

机构信息

Soochow Institute of Energy and Material Innovations, College of Energy, Soochow University, Suzhou, 215006, China.

Jiangsu Key Laboratory of Advanced Negative Carbon Technologies, Soochow University, Suzhou, 215123, Jiangsu, P. R. China.

出版信息

Angew Chem Int Ed Engl. 2023 Jul 10;62(28):e202305558. doi: 10.1002/anie.202305558. Epub 2023 Jun 1.

Abstract

Silicon semiconductor functionalized with molecular catalysts emerges as a promising cathode for photoelectrochemical (PEC) CO reduction reaction (CO 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 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 RR performance in contrast to the reported photocathodes functionalized with molecular catalysts.

摘要

功能化硅半导体与分子催化剂结合,成为光电化学(PEC)CO 还原反应(CO RR)有前途的阴极。然而,动力学和稳定性的限制仍然是此类复合材料发展的主要障碍。我们在此报告了一种通过化学接枝将导电石墨烯层接到 n-p Si 表面上,然后进行催化剂固定的硅光阴极组装策略。共价键合的石墨烯层有效地增强了阴极和还原催化剂之间的光生载流子转移,并提高了电极的工作稳定性。引人注目的是,我们证明通过煅烧改变固定化钴四苯基卟啉(CoTPP)催化剂的堆叠构型可以进一步提高电子转移率和 PEC 性能。最后,石墨烯涂覆的 Si 阴极固定化 CoTPP 催化剂在近中性电位(相对于可逆氢电极为-0.1 V)下的水中成功地维持了稳定的 1 太阳光电流为-1.65 mA cm,用于 CO 生产,持续 16 小时。与报道的功能化分子催化剂的光阴极相比,这代表了 PEC CO RR 性能的显著提高。

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