4.8 Article

Boosting Unassisted Alkaline Solar Water Splitting Using Silicon Photocathode with TiO2 Nanorods Decorated by Edge-Rich MoS2 Nanoplates

Journal

SMALL
Volume 17, Issue 39, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202103457

Keywords

hydrogen evolution; molybdenum disulfide; photoelectrochemical water splitting; silicon; tandem device

Funding

  1. National Research Foundation of Korea (NRF) - Korea government Ministry of Science and ICT (MSIT) [2021R1A2B5B03001851, 2018M3D1A1058793, 2019M3E6A1103818, 2020M2D8A206983011, 2021R1A4A3027878, 2021M3D1A2039641, 2021M3H4A1A03057403]
  2. National Research Foundation of Korea [2021M3H4A1A03057403, 2021R1A2B5B03001851, 2021M3D1A2039641, 2018M3D1A1058793] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study achieves stable and efficient solar water splitting in alkaline conditions by developing new catalysts and optimizing the structure of the silicon photocathode. The MoS2 nanoplates/TiO2 nanorods/p-Si photocathode shows high photoelectrochemical performance in alkaline media, with a high photocurrent density and stability, leading to a high solar-to-hydrogen efficiency when integrated with semiconductor photovoltaic cells.
To construct a highly efficient photoelectrochemical tandem device with silicon photocathode operating in alkaline conditions, it is desirable to develop stable and active catalysts which enable the photocathode to reliably perform under an alkaline environment. With nanostructured passivation layer and edge-exposed transition metal disulfides, silicon photocathode provides new opportunities for achieving unbiased alkaline solar water splitting. Here, the TiO2 nanorod arrays decorated by edge-rich MoS2 nanoplates are elaborately synthesized and deposited on p-Si. The vertically aligned TiO2 nanorods fully stabilize the Si surface and improve anti-reflectance. Moreover, MoS2 nanoplates with exposed edge sites provide catalytically active regions resulting in the kinetically favored hydrogen evolution under an alkaline environment. Interfacial energy band bending between p-Si and catalyst layers facilitates the transport of photogenerated electrons under steady-state illumination. Consequently, the MoS2 nanoplates/TiO2 nanorods/p-Si photocathode exhibits significantly improved photoelectrochemical-hydrogen evolution reaction (PEC-HER) performance in alkaline media with a high photocurrent density of 10 mA cm(-2) at 0 V versus RHE and high stability. By integrating rationally designed photocathode with earth-abundant Fe-60(NiCo)(30)Cr-10 anode and perovskite/Si tandem photovoltaic cell, an unassisted alkaline solar water splitting is accomplished with a current density of 5.4 mA cm(-2) corresponding to 6.6% solar-to-hydrogen efficiency, which is the highest among p-Si photocathodes.

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