4.8 Article

Plasma Oxidized Ti3C2Tx MXene as Electron Transport Layer for Efficient Perovskite Solar Cells

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 27, Pages 32495-32502

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c07146

Keywords

perovskite solar cell; Ti3C2Tx; MXene; plasma; electron transport layer

Funding

  1. National Natural Science Foundation of China [62004082, 61674070, 61722501]
  2. Fundamental Research Funds for the Central Universities [21619318, 21618313]
  3. Science and Technology Planning Project of Guangzhou China [201605030008]
  4. China Postdoctoral Science Foundation [2020M670036]

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Researchers utilized Ti3C2Tx MXene as the electron transport layer and conducted surface modification through oxygen plasma treatment. The treatment broke some Ti-C bonds, generating abundant Ti-O bonds and altering the surface properties of MXene, resulting in reduced trap states and improved electron transport. Contact angle and topography measurements were used to investigate the surface tension of MXene and the morphology of corresponding perovskite.
Recently, the two-dimensional material Ti3C2Tx MXene has attracted interest from researchers in perovskite solar cells (PSCs) with its great advantages in terms of high transmittance, high conductivity, tunable work function, and solution processability. However, the MXene-based PSC performance has still been inferior to that of the traditional TiO2 - or SnO2-based counterpart up until now. Some critical issues regarding to the MXene/perovskite interface still have not been well addressed. Herein, we used the Ti3C2Tx MXene as electron transport layer in PSCs via a room-temperature solution process followed by oxygen plasma treatment. Various characterization techniques were taken to establish the correlation between the surface properties and termination groups of MXene. We showed that oxygen plasma treatment could break parts of Ti-C bonds and generate abundant Ti-O bonds randomly distributed on MXene. The surface modification resulted in tunable work functions of MXene, as well as reduced trap states and improved electron transport close to the interface. In addition, the surface tension of MXene and corresponding perovskite morphology were thoroughly investigated by the contact angle and topography measurements. High-resolution XPS spectra indicated the Pb-O interactions between perovskite and MXene, which contributed to the device stability improvement.

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