The photoactive material was of significant
importance in organic
photoelectrochemical transistor (OPECT) bioanalysis as it influences
the photoinduced voltage and the μC* product,
resulting in a varying sensor sensitivity. The utilization of metal–organic
frameworks (MOFs) as photoactive materials in OPECT analysis is promising,
yet it remains a grand challenge due to the inherently narrow light
absorption range and high electron–hole recombination rate.
Herein, Pd NPs were encapsulated as electron acceptors into the Cu-MOF
using a double-solvent method, followed by pyrolysis at the proper
temperature. After pyrolysis, Cu-MOF transformed into a carbon defect-rich
composite of CuO and Cu2O while retaining its high porosity
and structural morphology. The resulting carbon defect-rich pyrolysis
Cu-MOF (p-Cu-MOF) served as an active support, facilitating the separation
of electrons and holes. The photoelectrons trigger the electron transfer
of adjacent active metal components and the formation of a Schottky
junction between Pd and the MOFs. This effect induces the electron
donation from the MOFs. Moreover, Pd/pyrolysis Cu-MOF exhibits significantly
higher visible light absorption, better water stability, and higher
electrical conductivity compared to Cu-MOF and Pd/Cu-MOF. An OPECT
sensor was fabricated by utilizing Pd/p-Cu-MOF as the photoactive
material and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate)
(PEDOT:PSS) as the channel material on an integrated laser-etched
FTO. The aptamer was used as the recognition element, enabling sensitive
and efficient detection of residual isocarbophos.