Suppr超能文献

由铜纳米片阵列支撑的用于全解水的有机光阴极。

Organic Photocathode Supported by Copper Nanosheets Array for Overall Water Splitting.

作者信息

Zhang Rui, Sun Xingjun, Zheng Lingcheng, Diao Lingxue, Chen Feifei, Li Yan, Wang Shuli, Wang Yajiang, Wang Weihua, Lu Feng, Dong Hong, Liu Hui, Cheng Yahui

机构信息

Department of Electronic Science and Engineering & Tianjin Key Laboratory of Green Chemistry and Pharmaceutical Process Control, Nankai University, Tianjin, 300350, P. R. China.

School of Mechanics and Photoelectric Physics, Anhui University of Science and Technology, Huainan, 232001, P. R. China.

出版信息

Chemistry. 2022 Jan 27;28(6):e202103495. doi: 10.1002/chem.202103495. Epub 2021 Dec 22.

Abstract

The Z-scheme overall solar water splitting is a mimic of natural photosynthesis to convert solar energy into chemical energy. Since the energy levels of most organic semiconductors match well with the hydrogen evolution potential, they have great application prospects as photocathodes in Z-scheme photoelectrochemical systems. However, due to the weak light absorption and difficult carrier separation, the photocurrent density and onset potential of organic photocathodes are still low. To solve these problems, we introduced a copper nanosheets array (Cu NSA) framework under organic layers to increase the surface reaction sites, improve the light absorption and enhance the distribution range of built-in electric field simultaneously. As a result, the photocurrent density and onset potential of poly(3-hexylthiophene) : [6,6]-phenyl-C -butyric acid (P3HT : PCBM) photocathode were enhanced significantly. The onset potential increased by 50 mV to 0.65 V vs. RHE, and the photocurrent density reached -1 mA cm at 0 V vs. RHE, which was 18 times that of the sample without Cu NSA. The optimized photocathode was connected with titanium dioxide nanorods array photoanode in a tandem manner to realize the spontaneous overall water splitting. Without bias and co-catalyst, the photocurrent density was maintained at 110 μA cm and the solar-to-fuel conversion efficiency was 0.14 % in neutral solution. These results provide a feasible method for optimizing the performance of organic photocathodes.

摘要

Z 型整体太阳能水分解是对自然光合作用的一种模仿,旨在将太阳能转化为化学能。由于大多数有机半导体的能级与析氢电位匹配良好,它们作为 Z 型光电化学系统中的光阴极具有巨大的应用前景。然而,由于光吸收较弱且载流子分离困难,有机光阴极的光电流密度和起始电位仍然较低。为了解决这些问题,我们在有机层下方引入了铜纳米片阵列(Cu NSA)框架,以增加表面反应位点、改善光吸收并同时增强内建电场的分布范围。结果,聚(3 - 己基噻吩):[6,6] - 苯基 - C - 丁酸(P3HT:PCBM)光阴极的光电流密度和起始电位得到了显著提高。相对于可逆氢电极(RHE),起始电位增加了 50 mV 至 0.65 V,并且在相对于 RHE 为 0 V 时,光电流密度达到 -1 mA cm,这是没有 Cu NSA 的样品的 18 倍。优化后的光阴极与二氧化钛纳米棒阵列光阳极串联连接,以实现自发的整体水分解。在中性溶液中,无偏压且无共催化剂的情况下,光电流密度保持在 110 μA cm,太阳能到燃料的转换效率为 0.14%。这些结果为优化有机光阴极的性能提供了一种可行的方法。

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