The
ability of MXenes to efficiently absorb light is greatly enriched
by the surface plasmons oscillating at their two-dimensional (2D)
surfaces. Thus far, MXenes have shown impressive plasmonic absorptions
spanning the visible and infrared (IR) regimes. However, their potential
use in IR optoelectronic applications, including photodiodes, has
been marginally investigated. Besides, their relatively low resistivity
has limited their use as photosensing materials due to their intrinsic
high dark current. Herein, heterostructures made of methylammonium
lead triiodide (MAPbI3) perovskite and niobium carbide
(Nb2CT
x
) MXene
are prepared with a matching band structure and exploited for self-powered
visible-near IR (NIR) photodiodes. Using MAPbI3 has expanded
the operation range of the MAPbI3/Nb2CT
x
photodiode to the visible
regime while suppressing the relatively large dark current of the
NIR-absorbing Nb2CT
x
. In consequence, the fabricated MAPbI3/Nb2CT
x
photodiode has responded
linearly to white light illumination with a responsivity of 0.25 A/W
and a temporal photoresponse of <4.5 μs. Furthermore, when
illuminated by NIR laser (1064 nm), our photodiode demonstrates a
higher on/off ratio (∼103) and faster response times
(<30 ms) compared to that of planar Nb2CT
x
-only detectors (<2 and 20 s, respectively).
The performed space-charge-limited current (SCLC) and capacitance
measurements reveal that such an efficient and enhanced charge transfer
depends on the coordinate bonding between the surface groups of the
MXene and the undercoordinated Pb2+ ions of the MAPbI3 at the passivated MAPbI3/Nb2CT
x
interface.