A highly selective self-powered sensor based on the upconversion nanoparticles/CdS nanospheres for chlorpyrifos detection.

Light sources are crucial for photoelectrochemical (PEC) self-powered sensing, where visible light is widely used. However, due to its high energy, it has some downsides as an irradiation source for overall system, so it is urgent to achieve effective near-infrared (NIR) light absorption because it makes up a significant portion of the solar spectrum. Herein, up-conversion nanoparticles (UCNPs) that could increase the energy of low-energy radiation were combined with semiconductor CdS as the photoactive material (UCNPs/CdS), which broadens the response range of solar spectrum. The NIR light-excited self-powered sensor could be produced via oxidizing H2O at photoanode and lowering dissolved oxygen at cathode under the NIR light without external voltage. Meanwhile, molecularly imprinted polymer (MIP) was added to photoanode as a recognition element to increase the sensor's selectivity. The open-circuit voltage of the self-powered sensor grew linearly as chlorpyrifos concentration climbed from 0.01 to 100 ng mL-1, showing good selectivity as well as reproducibility. This work provides valuable basis for the preparation of efficient and practical PEC sensor with NIR light response.

3D printed bionic self-powered sensing device based on fern-shaped nitrogen doped BiVO4 photoanode with enriched oxygen vacancies.

A portable three-dimensional (3D) printed bionic sensing device with enhanced photoelectric response was fabricated for sensitive detection of Bisphenol A (BPA). The proposed sensor is operated upon by using a highly reactive dual-electrode system to generate electrical output and provide the sensing signal under photoirradiation, without an external power source. The fern-shaped nitrogen doped BiVO4 photoanode with enriched oxygen vacancies (Ov) bismuth vanadate (N/Ov/BiVO4) photoanode was first synthesized and applied to construct a bionic sensing device. Density functional theoretical (DFT) calculation shows that the synergistic of nitrogen doping and Ov on the surface of photoanode leads to the emergence of impurity levels in BiVO4's electronic structure, promoting the effective separation of photogenerated electron-hole pairs. Impressively, the unique fern-shaped bionic structure enhances the mass transfer efficiency of the sensing system and provides abundant binding sites of aptamer, realizing signal amplification. Moreover, a portable sensing device for automatic sample injection and detection is developed by integrating the detection system into a micromodel based on micro-nano 3D printing technology. Benefit from this ingenious design, the proposed bionic aptasensor displayed excellent electricity output and achieved high sensitivity and selectivity of BPA detection with a low limit of detection (0.025 nM) and broad linear range from 0.1 nM to 100 µM, paving a new way for the development of portable and on-site sensing devices.

Self-Powered Photoelectrochemical Aptasensor for Oxytetracycline Cathodic Detection Based on a Dual Z-Scheme WO3/g-C3N4/MnO2 Photoanode.

With the high sensitivity and anti-interference provided by a dual Z-scheme structure photoanode and a two-electrode system, a high-performance self-powered photoelectrochemical (PEC) aptasensor for oxytetracycline (OTC) detection was established in this work. Graphitic carbon nitride (g-C3N4) with excellent photoelectric properties was used to be combined with WO3 and MnO2 to form a kind of dual Z-scheme heterojunction. The designed unique structure and the complementary performances of the three materials collectively guaranteed the highly stable photocurrent output of the photoanode due to the wide range of light absorption and the high separation rate of electron-hole pairs. The aptamer-based cathode modified with reduced graphene oxide (rGO) and Au nanoparticles (Au NPs) provided high conductivity and aptamer-binding sites, which brought excellent selective recognition of OTC as well as the self-powered capacity by receiving electrons from the photoanode. In the PEC sensing of OTC, the device presented a wide detection range from 1 pM to 150 nM and a low detection limit of 0.1 pM. Besides, the developed PEC aptasenor showed good selectivity, reproducibility, and stability, so as to be applied to real samples. The proposed PEC sensing method can be considered an effective and promising direction for the detection of antibiotics in the future.