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The development of a sensor capable of selectively detecting hydrogen levels in the environment holds immense importance for ensuring the safer utilization of hydrogen energy. In this study, a hydrogen sensor made of Ce-doped single-layer graphene (SLG)/SnO2 composite material was fabricated using a hydrothermal method. The study examined the impact of varying Ce doping concentrations on the hydrogen sensing capabilities of the SLG/SnO2 matrix. The results show that the SLG/SnO2 hydrogen sensor doped with 2 mol% Ce demonstrated optimal performance at a humidity of 20%. It operated most efficiently at 250 °C, with a response of 2.49, representing a 25.75% improvement over the undoped sample. The response/recovery times were 0.46/3.92 s, which are 54.9% shorter than those of the undoped sample. The enhancement in hydrogen sensitivity stems from the synergistic effect of Ce and SLG, which facilitates the coexistence of n–n and p–n heterojunctions, thereby increasing carrier mobility and refining grain structure. Analysis via X-ray photoelectron spectroscopy (XPS) reveals that Ce increases the material’s oxygen vacancy concentration, enhancing its hydrogen sensitivity. Ce-doped SLG/SnO2, with its robust hydrogen sensitivity, represents one of the leading candidates for future hydrogen gas sensors.

Using a p-n heterojunction is one of the efficient methods to increase charge transfer in photocatalysis applications. So, herein, p-type UiO-66 (NH2) and n-type CuFe2O4 (CFO) are used to form an effective p-n heterojunction. Due to their poor charge separation in their pristine form, both UiO-66 (NH2) and CFO materials cannot produce hydrogen; however, the composite p-n heterojunction formed between these materials makes fast charge separation and so hydrogen is efficiently produced. The optimized catalyst UCFO 25% produces a maximum of 62.5 µmol/g/h hydrogen in an aqueous methanol solution. The formation of a p-n heterojunction is confirmed by Mott–Schottky analysis and optical properties, crystallinity and the local atomic environment of the material was analyzed by various analytical tools like UV-Vis spectroscopy, XRD, and XANES.

A rapid and accurate monitoring of hazardous formaldehyde (HCHO) gas is extremely essential for health protection. However, the high-power consumption and humidity interference still hinder the application of HCHO gas sensors. Hence, zeolitic imidazolate framework-8 (ZIF-8)-loaded Pt-NiO/In2O3 hollow nanofibers (ZPNiIn HNFs) were designed via the electrospinning technique followed by hydrothermal treatment, aiming to enable a synergistic advantage of the surface modification and the construction of a p-n heterostructure to improve the sensing performance of the HCHO gas sensor. The ZPNiIn HNF sensor has a response value of 52.8 to 100 ppm HCHO, a nearly 4-fold enhancement over a pristine In2O3 sensor, at a moderately low temperature of 180 °C, along with rapid response/recovery speed (8/17 s) and excellent humidity tolerance. These enhanced sensing properties can be attributed to the Pt catalysts boosting the catalytic activity, the p-n heterojunctions facilitating the chemical reaction, and the appropriate ZIF-8 loading providing a hydrophobic surface. Our research presents an effective sensing material design strategy for inspiring the development of cost-effective sensors for the accurate detection of indoor HCHO hazardous gas.

Two-dimensional transition metal dichalcogenides (2D-TMDs) possess appropriate bandgaps and interact via van der Waals (vdW) forces between layers, effectively overcoming lattice compatibility challenges inherent in traditional heterojunctions. This property facilitates the creation of heterojunctions with customizable bandgap alignments. However, the prevailing method for creating heterojunctions with 2D-TMDs relies on the low-efficiency technique of mechanical exfoliation. Sb2Te3, recognized as a notable p-type semiconductor, emerges as a versatile component for constructing diverse vertical p–n heterostructures with 2D-TMDs. This study presents the successful large-scale deposition of 2D Sb2Te3 onto inert mica substrates, providing valuable insights into the integration of Sb2Te3 with 2D-TMDs to form heterostructures. Building upon this initial advancement, a precise epitaxial growth method for Sb2Te3 on pre-existing WS2 surfaces on SiO2/Si substrates is achieved through a two-step chemical vapor deposition process, resulting in the formation of Sb2Te3/WS2 heterojunctions. Finally, the development of 2D Sb2Te3/WS2 optoelectronic devices is accomplished, showing rapid response times, with a rise/decay time of 305 μs/503 μs, respectively.

The combination of two-dimensional material MXene and one-dimensional metal oxide semiconductor can improve the carrier transmission rate, which can effectively improve sensing performance. We prepared a trimethylamine gas sensor based on MoO3 nanofibers and layered Ti3C2Tx MXene. Using electrospinning and chemical etching methods, one-dimensional MoO3 nanofibers and two-dimensional Ti3C2Tx MXene nanosheets were prepared, respectively, and the composites were characterized via XPS, SEM, and TEM. The Ti3C2Tx MXene–MoO3 composite material exhibits excellent room-temperature response characteristics to trimethylamine gas, showing high response (up to four for 2 ppm trimethylamine gas) and rapid response–recovery time (10 s/7 s). Further, we have studied the possible sensitivity mechanism of the sensor. The Ti3C2Tx MXene–MoO3 composite material has a larger specific surface area and more abundant active sites, combined with p–n heterojunction, which effectively improves the sensitivity of the sensor. Because of its low detection limit and high stability, it has the potential to be applied in the detection system of trimethylamine as a biomarker in exhaled air.

Morphology and structure play a crucial role in influencing the performance of gas sensors. Hollow structures, in particular, not only increase the specific surface area of the material but also enhance the collision frequency of gases within the shell, and have been studied in depth in the field of gas sensing. Taking SnO2 as an illustrative example, a dual-shell structure SnO2 (D-SnO2) was prepared. D-SnO2@Polyaniline (PANI) (DSPx, x represents D-SnO2 molar content) composites were synthesized via the in situ oxidative polymerization method, and simultaneously deposited onto a polyethylene terephthalate (PET) substrate to fabricate an electrode-free, flexible sensor. The impact of the SnO2 content on the sensing performance of the DSPx-based sensor for NH3 detection at room temperature was discussed. The results showed that the response of a 20 mol% D-SnO2@PANI (DSP20) sensor to 100 ppm NH3 at room temperature is 37.92, which is 5.1 times higher than that of a pristine PANI sensor. Moreover, the DSP20 sensor demonstrated a rapid response and recovery rate at the concentration of 10 ppm NH3, with response and recovery times of 182 s and 86 s.

The aim of this work was to investigate a new, simple, one-pot combustion synthesis technique for creating sulphur-based CuS/ZnS p-n heterojunction nanocomposite photocatalysts. This study examined the photocatalytic activity and reusability of these nanocomposites in removing rhodamine B (RhB) dye under visible-light irradiation. Various methods of characterisation were employed to determine the properties of the materials, including particle morphology, crystalline phases, and bandgap energy. The intrinsic reaction parameters, such as catalyst loading, the pH level of the solution, and initial pollutant concentration, were varied to establish the optimal photodegradation conditions. The results showed that a binary CuS/ZnS catalyst with a 10 g L−1 loading, at pH 5, degraded 97% of 5 ppm RhB dye after 270 min of visible light irradiation. Additionally, this composite catalyst exhibited excellent chemical stability and reusability, achieving 83% RhB dye removal after five recycling runs. Scavenger tests identified the photogenerated holes (h+) and superoxide free radicals (•O2) as the primary reactive species responsible for degradation. This study provides valuable insight into the design of highly efficient nanomaterials for removing organic pollutants in wastewater, and a possible reaction mechanism is proposed.

In this study, a Z-Scheme WO3/CoO p-n heterojunction with a 0D/3D structure was designed and prepared via a simple solvothermal approach to remove the combined pollution of tetracycline and heavy metal Cr(VI) in water. The 0D WO3 nanoparticles adhered to the surface of the 3D octahedral CoO to facilitate the construction of Z-scheme p-n heterojunctions, which could avoid the deactivation of the monomeric material due to agglomeration, extend the optical response range, and separate the photogenerated electronhole pairs. The degradation efficiency of mixed pollutants after a 70 min reaction was significantly higher than that of monomeric TC and Cr(VI). Among them, a 70% WO3/CoO heterojunction had the best photocatalytic degradation effect on the mixture of TC and Cr(VI) pollutants, and the removing rate was 95.35% and 70.2%, respectively. Meanwhile, after five cycles, the removal rate of the mixed pollutants by the 70% WO3/CoO remained almost unchanged, indicating that the Z-scheme WO3/CoO p-n heterojunction has good stability. In addition, for an active component capture experiment, ESR and LC-MS were employed to reveal the possible Z-scheme pathway under the built-in electric field of the p-n heterojunction and photocatalytic removing mechanism of TC and Cr(VI). These results offer a promising idea for the treatment of the combined pollution of antibiotics and heavy metals by a Z-scheme WO3/CoO p-n heterojunction photocatalyst, and have broad application prospects: boosted tetracycline and Cr(VI) simultaneous cleanup over a Z-scheme WO3/CoO p-n heterojunction with a 0D/3D structure under visible light.

A p–n heterojunction semiconductor structure composed of Ce3O4 and BiVO4 has been synthesized and then incorporated into reduced graphene oxide (rGO) by the hydrothermal method. The ternary composites were characterized by X-ray diffraction, transmission electron microscopy (TEM), scanning electron microscopy (SEM), electron diffraction spectroscopy (EDS), and UV–vis spectroscopy. The efficiency of the composites as photocatalysts was determined by studying the oxidative degradation of methyl orange in aqueous solution under visible light irradiation. The effect of parameters such as pH, catalyst loading, and concentration of the dye solution was examined in order to determine their influence on the photocatalytic activity of the composites. The composite incorporated into reduced graphene oxide presented the highest percentage (above 90%) in 2 h time, attributed to the effect of the increased surface area. The process of the enhanced photocatalytic activity has been discussed based on the energy band positions of the nanoparticles within the composite.

The S-scheme photocatalyst system has become increasingly popular in recent years for its ability to efficiently degrade various pollutants, including organic dyes, pesticides, and other harmful substances. This system uses two semiconductor photocatalysts with different bandgap energies, working together in a redox reaction to produce a highly reactive species capable of pollutant breakdown. Here, an S-scheme Ag2WO4/Ag6Si2O7 p-n heterojunction nanocomposite was successfully developed by a coprecipitation method. By decomposing Rhodamine B (RhB) under visible-light irradiation, the photocatalytic activities of Ag6Si2O7/Ag2WO4 showed enhanced photocatalytic degradation performance of organic dyes, especially at a 4% molar ratio of the Ag2WO4-modified Ag6Si2O7 sample, whose degradation rate was 23.7 and 4.65 times those of Ag2WO4 and Ag6Si2O7, respectively. The physical and chemical properties of the samples were determined by identifying the physical structure, chemical element composition, and optical responsiveness. The optimum composite amongst the prepared materials was AgSW-4, achieving the maximum RhB degradation efficiency of 97.5%, which was higher by 60% and 20% than its counterparts Ag6Si2O7 and Ag2WO4, respectively. These results showed that in the nanocomposite structure, Ag6Si2O7 was a p-type semiconductor and Ag2WO4 was an n-type semiconductor. Based on the analysis data, a comprehensive p-n heterojunction S-scheme process was proposed to demonstrate the enhanced photocatalytic performance of the Ag6Si2O7/Ag2WO4 nanocomposite.

High photoelectrochemical water oxidation efficiency can be achieved through an efficient photogenerated holes transfer pathway. Constructing a photoanode semiconductor heterojunction with close interface contact is an effective tactic to improve the efficiency of photogenerated carrier separation. Here, we reported a novel photoanode p-n junction of Ti:Fe2O3/Cu2O (n-Ti:Fe2O3 and p-Cu2O), Cu2O being obtained by in situ reduction in CuAl-LDH (layered double hydroxides). The Ti:Fe2O3/Cu2O photoanode exhibits a high photocurrent density reaching 1.35 mA/cm2 at 1.23 V vs. RHE is about 1.67 and 50 times higher than the Ti:Fe2O3 and α-Fe2O3 photoanode, respectively. The enhanced PEC activity for the n-Ti:Fe2O3/p-Cu2O photoelectrode is due to the remarkable surface charge separation efficiency (ηsurface 85%) and bulk charge separation efficiency (ηbulk 72%) formed by the p-n junction and the tight interface contact formed by in situ reduction. Moreover, as a cocatalyst, CuAl-LDH can protect the Ti:Fe2O3/Cu2O photoanode and improve its stability to a certain extent. This study provides insight into the manufacturing potential of in situ reduction layered double hydroxides semiconductor for designing highly active photoanodes in the field of photoelectrochemical water oxidation.

Photocatalysts derived from semiconductor heterojunctions for water splitting have bright prospects in solar energy conversion. Here, a Co3O4@ZIS p-n heterojunction was successfully created by developing two-dimensional ZnIn2S4 on ZIF-67-derived hollow Co3O4 nanocages, realizing efficient spatial separation of the electron-hole pair. Moreover, the black hollow structure of Co3O4 considerably increases the range of light absorption and the light utilization efficiency of the heterojunction avoids the agglomeration of ZnIn2S4 nanosheets and further improves the hydrogen generation rate of the material. The obtained Co3O4(20) @ZIS showed excellent photocatalytic H2 activity of 5.38 mmol g−1·h−1 under simulated solar light, which was seven times more than that of pure ZnIn2S4. Therefore, these kinds of constructions of hollow p-n heterojunctions have a positive prospect in solar energy conversion fields.

Herein, CuS was incorporated with ZnS to form a novel nanocomposite via cation exchange, and the product was then employed for dual application of the colorimetric determination and photocatalytic degradation of tetracycline (TC) in water. The formed p–n heterojunction provided an improved gap width and electron mobility, which could rapidly catalyze H2O2 to produce plenty of •OH, supporting a color conversion with TMB. Meanwhile, the addition of TC could lead to the further enhancement in colorimetric signal, and the distinction level was sensitive to the target amount. Additionally, under light conditions, the p-CuS/n-ZnS could produce •O2−, •OH, and h+ through photocatalysis, and these ions could degrade the TC via oxidation. In the colorimetric determination of TC, the signal responses were obtained within 10 min, and the detection limit was 20.94 nM. The recovery rates were 99% and 106% for the water samples from Ganjiang river. In the photocatalytic degradation, the TC was degraded by 91% within 120 min, which was threefold that of ZnS. Meanwhile, the morphology feature of the p-CuS/n-ZnS remained after multiple uses, suggesting a favorable material stability. This strategy provides application prospects for the monitoring and control of antibiotics in water.

Constructing heterojunction is an attractive strategy for promoting photoelectrochemical (PEC) performance in water splitting and organic pollutant degradation. Herein, a novel porous BiVO4/Boron-doped Diamond (BiVO4/BDD) heterojunction photoanode containing masses of ultra-micro electrodes was successfully fabricated with an n-type BiVO4 film coated on a p-type BDD substrate by magnetron sputtering (MS). The surface structures of BiVO4 could be adjusted by changing the duration of deposition (Td). The morphologies, phase structures, electronic structures, and chemical compositions of the photoanodes were systematically characterized and analyzed. The best PEC activity with the highest current density of 1.8 mA/cm2 at 1.23 VRHE was achieved when Td was 30 min, and the sample showed the highest degradation efficiency towards tetracycline hydrochloride degradation (TCH) as well. The enhanced PEC performance was ascribed to the excellent charge transport efficiency as well as a lower carrier recombination rate, which benefited from the formation of BiVO4/BDD ultra-micro p-n heterojunction photoelectrodes and the porous structures of BiVO4. These novel photoanodes were expected to be employed in the practical PEC applications of energy regeneration and environmental management in the future.

Layered perovskite-type semiconductor La2Ti2O7 has attracted lots of attention in photocatalytic hydrogen evolution, due to the suitable energy band position for water splitting, high specific surface area, and excellent physicochemical stability. However, the narrow light absorption range and the low separation efficiency of photogenerated carriers limit its photocatalytic activity. Herein, plate-like La2Ti2O7 with uniform crystal morphology was synthesized in molten NaCl salt. A p-n heterojunction was then constructed through the in situ hydrothermal growth of p-type Co3O4 nanoparticles on the surface of n-type plate-like La2Ti2O7. The effects of Co3O4 loading on photocatalytic hydrogen evolution performance were investigated in detail. The results demonstrate that composite Co3O4/La2Ti2O7 possesses much better photocatalytic activity than the pure component. The composite photocatalyst with 1 wt% Co3O4 exhibits the highest hydrogen evolution rate of 79.73 μmol·g−1·h−1 and a good cycling stability. The photoelectrochemistry characterizations illustrate that the improvement of photocatalytic activity is mainly attributed to both the enhanced light absorption from the Co3O4 ornament and the rapid separation of photogenerated electron-hole pairs driven by the built-in electric field close to the p-n heterojunction. The results may provide further insights into the design of high-efficiency La2Ti2O7-based heterojunctions for photocatalytic hydrogen evolution.

Self-powered ultraviolet (UV) photodetectors have attracted considerable attention in recent years because of their vast applications in the military and civil fields. Among them, self-powered UV photodetectors based on p-n heterojunction low-dimensional nanostructures are a very attractive research field due to combining the advantages of low-dimensional semiconductor nanostructures (such as large specific surface area, excellent carrier transmission channel, and larger photoconductive gain) with the feature of working independently without an external power source. In this review, a selection of recent developments focused on improving the performance of self-powered UV photodetectors based on p-n heterojunction low-dimensional nanostructures from different aspects are summarized. It is expected that more novel, dexterous, and intelligent photodetectors will be developed as soon as possible on the basis of these works.

Two-dimensional transition metal dichalcogenides (2D-TMDs) possess appropriate bandgaps and interact via van der Waals (vdW) forces between layers, effectively overcoming lattice compatibility challenges inherent in traditional heterojunctions. This property facilitates the creation of heterojunctions with customizable bandgap alignments. However, the prevailing method for creating heterojunctions with 2D-TMDs relies on the low-efficiency technique of mechanical exfoliation. Sb 2 Te 3 , recognized as a notable p-type semiconductor, emerges as a versatile component for constructing diverse vertical p-n heterostructures with 2D-TMDs. This study presents the successful large-scale deposition of 2D Sb 2 Te 3 onto inert mica substrates, providing valuable insights into the integration of Sb 2 Te 3 with 2D-TMDs to form heterostructures. Building upon this initial advancement, a precise epitaxial growth method for Sb 2 Te 3 on pre-existing WS 2 surfaces on SiO 2 /Si substrates is achieved through a two-step chemical vapor deposition process, resulting in the formation of Sb 2 Te 3 /WS 2 heterojunctions. Finally, the development of 2D Sb 2 Te 3 /WS 2 optoelectronic devices is accomplished, showing rapid response times, with a rise/decay time of 305 μs/503 μs, respectively.

A rapid and accurate monitoring of hazardous formaldehyde (HCHO) gas is extremely essential for health protection. However, the high-power consumption and humidity interference still hinder the application of HCHO gas sensors. Hence, zeolitic imidazolate framework-8 (ZIF-8)-loaded Pt-NiO/In 2 O 3 hollow nanofibers (ZPNiIn HNFs) were designed via the electrospinning technique followed by hydrothermal treatment, aiming to enable a synergistic advantage of the surface modification and the construction of a p-n heterostructure to improve the sensing performance of the HCHO gas sensor. The ZPNiIn HNF sensor has a response value of 52.8 to 100 ppm HCHO, a nearly 4-fold enhancement over a pristine In 2 O 3 sensor, at a moderately low temperature of 180 °C, along with rapid response/recovery speed (8/17 s) and excellent humidity tolerance. These enhanced sensing properties can be attributed to the Pt catalysts boosting the catalytic activity, the p-n heterojunctions facilitating the chemical reaction, and the appropriate ZIF-8 loading providing a hydrophobic surface. Our research presents an effective sensing material design strategy for inspiring the development of cost-effective sensors for the accurate detection of indoor HCHO hazardous gas.

The combination of two-dimensional material MXene and one-dimensional metal oxide semiconductor can improve the carrier transmission rate, which can effectively improve sensing performance. We prepared a trimethylamine gas sensor based on MoO 3 nanofibers and layered Ti 3 C 2 T x MXene. Using electrospinning and chemical etching methods, one-dimensional MoO 3 nanofibers and two-dimensional Ti 3 C 2 T x MXene nanosheets were prepared, respectively, and the composites were characterized via XPS, SEM, and TEM. The Ti 3 C 2 T x MXene-MoO 3 composite material exhibits excellent room-temperature response characteristics to trimethylamine gas, showing high response (up to four for 2 ppm trimethylamine gas) and rapid response-recovery time (10 s/7 s). Further, we have studied the possible sensitivity mechanism of the sensor. The Ti 3 C 2 T x MXene-MoO 3 composite material has a larger specific surface area and more abundant active sites, combined with p-n heterojunction, which effectively improves the sensitivity of the sensor. Because of its low detection limit and high stability, it has the potential to be applied in the detection system of trimethylamine as a biomarker in exhaled air.

Photocatalytic water splitting for hydrogen production has been widely recognized as a promising strategy for relieving the pressure from energy crisis and environmental pollution. However, current efficiency for photocatalytic hydrogen generation has been limited due to a low separation of photogenerated electrons and holes. p-n heterojunction with a built-in electric field emerges as an efficient strategy for photocatalyst design to boost hydrogen evolution activities due to a spontaneous charge separation. In this work, we investigated the effect of different preparation methods on photocatalytic hydrogen production over NiO-TiO2 composites. The results demonstrated that a uniform distribution of NiO on a surface of TiO2 with an intimate interfacial interaction was formed by a sol-gel method, while direct calcination tended to form aggregation of NiO, thus leading to an uneven p-n heterojunction structure within a photocatalyst. NiO-TiO2 composites fabricated by different methods showed enhanced hydrogen production (23.5 ± 1.2, 20.4 ± 1.0 and 8.8 ± 0.7 mmolh−1g−1 for S1-20%, S2-20% and S3-10%, respectively) as compared with pristine TiO2 (6.6 ± 0.7 mmolh−1g−1) and NiO (2.1 ± 0.2 mmolh−1g−1). The current work demonstrates a good example to improve photocatalytic hydrogen production by finely designing p-n heterojunction photocatalysts.

Novel heterojunction photocatalysts with remarkable photocatalytic capabilities and durability for degrading recalcitrant contaminants are extremely desired; however, their development still remains quite challenging. In this study, a series of flower-like BiOI/BiOCOOH p−n heterojunctions were fabricated via a controlled in situ anion-exchange process. During the process, BiOI formation and even deposition on BiOCOOH microspheres with tight interfacial contact were realized. As expected, BiOI/BiOCOOH heterojunctions revealed remarkable enhancements in photocatalytic antibiotic degradation capacities under visible light irradiation compared with pristine BiOI and BiOCOOH. The best-performing BiOI/BiOCOOH heterojunction (i.e., IBOCH-2) showed much improved photocatalytic CIP degradation efficiency of approximately 81- and 3.9-fold greater than those of bare BiOI and BiOCOOH, respectively. The eminent photocatalytic performances were due not only to the enhanced capability in harvesting photon energies in visible light regions, but also the accelerated separation of electrons and holes boosted by the p−n heterojunction. Active species trapping tests demonstrated that superoxide free radicals (•O2−) and photo-generated holes (h+) were major active species for CIP degradation. Recycling experiments verified the good durability of BIBO-2 over four runs. The facile in situ synthesis route and excellent performance endow flower-like BiOI/BiOCOOH heterojunctions with a promising potential for actual environmental remediation.

Gallium nitride (GaN) is a superior candidate material for fabricating ultraviolet (UV) photodetectors (PDs) by taking advantage of its attractive wide bandgap (3.4 eV) and stable chemical and physical properties. However, the performance of available GaN-based UV PDs (e.g., in terms of detectivity and sensitivity) still require improvement. Fabricating nanoporous GaN (porous-GaN) structures and constructing organic/inorganic hybrids are two effective ways to improve the performance of PDs. In this study, a novel self-powered UV PD was developed by using p-type cobalt phthalocyanine (CoPc) and n-type porous-GaN (CoPc/porous-GaN) to construct a p–n vertical heterojunction via a thermal vapor deposition method. Under 365 nm 0.009 mWcm−2 light illumination, our device showed a photoresponsivity of 588 mA/W, a detectivity of 4.8 × 1012 Jones, and a linear dynamic range of 79.5 dB, which are better than CoPc- and flat-GaN (CoPc/flat-GaN)-based PDs. The high performance was mainly attributed to the built-in electric field (BEF) generated at the interface of the CoPc film and the nanoporous-GaN, as well as the nanoporous structure of GaN, which allows for a higher absorptivity of light. Furthermore, the device showed excellent stability, as its photoelectrical property and on/off switching behavior remained the same, even after 3 months.

Photocatalytic technology has been considered to be an ideal approach to solve the energy and environmental crises, and TiO2 is regarded as the most promising photocatalyst. Compared with bare TiO2, TiO2 based p-n heterojunction exhibits a much better performance in charge separation, light absorption and photocatalytic activity. Herein, we developed an efficient method to prepare p-type TiO2 quantum dots (QDs) and decorated graphitic carbonitrile (g-C3N4) nanocomposites, while the composition and structure of the TiO2@g-C3N4 were analyzed by X-ray diffraction, Fourier transform infrared spectroscopy ,thermogravimetric analysis, transmission electron microscopy, X-ray photoelectron spectroscopy and UV-visible diffuse reflectance spectroscopy characterizations. The characterization results reveal the surface decorated TiO2 quantum dots is decomposed by titanium glycerolate, which exhibits p-type conductivity. The presence of p-n heterojunction over interface is confirmed, and photoluminescence results indicate a better performance in transfer and separation of photo-generated charge carriers than pure semiconductors and type-II heterojunction. Moreover, the synergy of p-n heterojunction over interface, strong interface interaction, and quantum-size effect significantly contributes to the promoted performance of TiO2 QDs@g-C3N4 composites. As a result, the as-fabricated TiO2 QDs@g-C3N4 composite with a p/n mass ratio of 0.15 exhibits improved photo-reactivity of 4.3-fold and 5.4-fold compared to pure g-C3N4 in degradation of organic pollutant under full solar spectrum and visible light irradiation, respectively.

Metal oxide p-n heterojunction nanofibers (NFs) are among the most promising approaches to enhancing the efficiency of gas sensors. In this paper, we report the preparation of a series of p-NiO-loaded n-ZnO NFs, namely (1−x)ZnO-xNiO (x = 0.03, 0.05, 0.7, 0.1, and 0.15 wt%), for hydrogen gas sensing experiments. Samples were prepared through the electrospinning technique followed by a calcination process. The sensing experiments showed that the sample with 0.05 wt% NiO loading resulted in the highest sensing performance at an optimal sensing temperature of 200 °C. The sensing mechanism is discussed in detail and contributions of the p-n heterojunctions, metallization of ZnO and catalytic effect of NiO on the sensing enhancements of an optimized gas sensor are analyzed. This study demonstrates the possibility of fabricating high-performance H2 sensors through the optimization of p-type metal oxide loading on the surfaces of n-type metal oxides.

There is a need for highly efficient photocatalysts, particularly for water purification. In this study, we fabricated a mesoporous TiO2 thin film on a boron-doped diamond (BDD) layer by a surfactant-assisted sol-gel method, in which self-assembled amphiphilic surfactant micelles were used as an organic template. Scanning electron microscopy revealed uniform mesopores, approximately 20 nm in diameter, that were hexagonally packed in the TiO2 thin film. Wide-angle X-ray diffraction and Raman spectroscopy clarified that the framework crystallized in the anatase phase. Current⁻voltage (I⁻V) measurements showed rectification features at the TiO2/BDD heterojunction, confirming that a p⁻n hetero-interface formed. The as-synthesized mesoporous TiO2/BDD worked well as a photocatalyst, even with a small volume of TiO2 (15 mm × 15 mm × c.a. 1.5 µm in thickness). The use of deep UV light (λ = 222 nm) as a light source was necessary to enhance photocatalytic activity, due to photo-excitation occurring in both BDD and TiO2.

A new and simple procedure for the deposition of lead (II, IV) oxide films by screen printing was developed. In contrast to conventional electrochemical methods, films can be also deposited on non-conductive substrates without any specific dimensional restriction, being the only requirement the thermal stability of the substrate in air up to 500 °C to allow for the calcination of the screen printing paste and sintering of the film. In this study, films were exploited for the preparation of both photoresponsive devices and photoelectrochemical cell photoanodes. In both cases, screen printing was performed on FTO (Fluorine-Tin Oxide glass) substrates. The photoresponsive devices were tested with I-V curves in dark and under simulated solar light with different irradiation levels. Responses were evaluated at different voltage biases and under light pulses of different durations. Photoelectrochemical cells were tested by current density–voltage (J-V) curves under air mass (AM) 1.5 G illumination, incident photon-to-current efficiency (IPCE) measurements, and electrochemical impedance spectroscopy.

Photocatalysts derived from semiconductor heterojunctions for water splitting have bright prospects in solar energy conversion. Here, a Co 3 O 4 @ZIS p-n heterojunction was successfully created by developing two-dimensional ZnIn 2 S 4 on ZIF-67-derived hollow Co 3 O 4 nanocages, realizing efficient spatial separation of the electron-hole pair. Moreover, the black hollow structure of Co 3 O 4 considerably increases the range of light absorption and the light utilization efficiency of the heterojunction avoids the agglomeration of ZnIn 2 S 4 nanosheets and further improves the hydrogen generation rate of the material. The obtained Co 3 O 4 (20) @ZIS showed excellent photocatalytic H 2 activity of 5.38 mmol g -1 ·h -1 under simulated solar light, which was seven times more than that of pure ZnIn 2 S 4 . Therefore, these kinds of constructions of hollow p-n heterojunctions have a positive prospect in solar energy conversion fields.

Solar radiation is a cheap and abundant energy for water remediation, hydrogen generation by water splitting, and CO 2 reduction. Supported photocatalysts have to be tuned to the pollutants to be eliminated. Spectral engineering may be a handy tool to increase the efficiency or the selectivity of these. Photonic nanoarchitectures of biological origin with hierarchical organization from nanometers to centimeters are candidates for such applications. We used the blue wing surface of laboratory-reared male Polyommatus icarus butterflies in combination with atomic layer deposition (ALD) of conformal ZnO coating and octahedral Cu 2 O nanoparticles (NP) to explore the possibilities of engineering the optical and catalytic properties of hybrid photonic nanoarchitectures. The samples were characterized by UV-Vis spectroscopy and optical and scanning electron microscopy. Their photocatalytic performance was benchmarked by comparing the initial decomposition rates of rhodamine B. Cu 2 O NPs alone or on the butterfly wings, covered by a 5 nm thick layer of ZnO, showed poor performance. Butterfly wings, or ZnO coated butterfly wings with 15 nm ALD layer showed a 3 to 3.5 times enhancement as compared to bare glass. The best performance of almost 4.3 times increase was obtained for the wings conformally coated with 15 nm ZnO, deposited with Cu 2 O NPs, followed by conformal coating with an additional 5 nm of ZnO by ALD. This enhanced efficiency is associated with slow light effects on the red edge of the reflectance maximum of the photonic nanoarchitectures and with enhanced carrier separation through the n-type ZnO and the p-type Cu 2 O heterojunction. Properly chosen biologic photonic nanoarchitectures in combination with carefully selected photocatalyst(s) can significantly increase the photodegradation of pollutants in water under visible light illumination.

p-BiOI nanosheets/n-TiO2 nanofibers (p-BiOI/n-TiO2 NFs) have been facilely prepared via the electrospinning technique combining successive ionic layer adsorption and reaction (SILAR). Dense BiOI nanosheets with good crystalline and width about 500 nm were uniformly assembled on TiO2 nanofibers at room temperature. The amount of the heterojunctions and the specific surface area were well controlled by adjusting the SILAR cycles. Due to the synergistic effect of p-n heterojunctions and high specific surface area, the obtained p-BiOI/n-TiO2 NFs exhibited enhanced visible-light photocatalytic activity. Moreover, the p-BiOI/n-TiO2 NFs heterojunctions could be easily recycled without decreasing the photocatalytic activity owing to their one-dimensional nanofibrous structure. Based on the above, the heterojunctions of p-BiOI/n-TiO2 NFs may be promising visible-light-driven photocatalysts for converting solar energy to chemical energy in environment remediation.

Herein, CuS was incorporated with ZnS to form a novel nanocomposite via cation exchange, and the product was then employed for dual application of the colorimetric determination and photocatalytic degradation of tetracycline (TC) in water. The formed p-n heterojunction provided an improved gap width and electron mobility, which could rapidly catalyze H 2 O 2 to produce plenty of •OH, supporting a color conversion with TMB. Meanwhile, the addition of TC could lead to the further enhancement in colorimetric signal, and the distinction level was sensitive to the target amount. Additionally, under light conditions, the p-CuS/n-ZnS could produce •O 2 - , •OH, and h + through photocatalysis, and these ions could degrade the TC via oxidation. In the colorimetric determination of TC, the signal responses were obtained within 10 min, and the detection limit was 20.94 nM. The recovery rates were 99% and 106% for the water samples from Ganjiang river. In the photocatalytic degradation, the TC was degraded by 91% within 120 min, which was threefold that of ZnS. Meanwhile, the morphology feature of the p-CuS/n-ZnS remained after multiple uses, suggesting a favorable material stability. This strategy provides application prospects for the monitoring and control of antibiotics in water.

Layered perovskite-type semiconductor La 2 Ti 2 O 7 has attracted lots of attention in photocatalytic hydrogen evolution, due to the suitable energy band position for water splitting, high specific surface area, and excellent physicochemical stability. However, the narrow light absorption range and the low separation efficiency of photogenerated carriers limit its photocatalytic activity. Herein, plate-like La 2 Ti 2 O 7 with uniform crystal morphology was synthesized in molten NaCl salt. A p-n heterojunction was then constructed through the in situ hydrothermal growth of p-type Co 3 O 4 nanoparticles on the surface of n-type plate-like La 2 Ti 2 O 7 . The effects of Co 3 O 4 loading on photocatalytic hydrogen evolution performance were investigated in detail. The results demonstrate that composite Co 3 O 4 /La 2 Ti 2 O 7 possesses much better photocatalytic activity than the pure component. The composite photocatalyst with 1 wt% Co 3 O 4 exhibits the highest hydrogen evolution rate of 79.73 μmol·g -1 ·h -1 and a good cycling stability. The photoelectrochemistry characterizations illustrate that the improvement of photocatalytic activity is mainly attributed to both the enhanced light absorption from the Co 3 O 4 ornament and the rapid separation of photogenerated electron-hole pairs driven by the built-in electric field close to the p-n heterojunction. The results may provide further insights into the design of high-efficiency La 2 Ti 2 O 7 -based heterojunctions for photocatalytic hydrogen evolution.

Self-powered ultraviolet (UV) photodetectors have attracted considerable attention in recent years because of their vast applications in the military and civil fields. Among them, self-powered UV photodetectors based on p-n heterojunction low-dimensional nanostructures are a very attractive research field due to combining the advantages of low-dimensional semiconductor nanostructures (such as large specific surface area, excellent carrier transmission channel, and larger photoconductive gain) with the feature of working independently without an external power source. In this review, a selection of recent developments focused on improving the performance of self-powered UV photodetectors based on p-n heterojunction low-dimensional nanostructures from different aspects are summarized. It is expected that more novel, dexterous, and intelligent photodetectors will be developed as soon as possible on the basis of these works.

Novel heterojunction photocatalysts with remarkable photocatalytic capabilities and durability for degrading recalcitrant contaminants are extremely desired; however, their development still remains quite challenging. In this study, a series of flower-like BiOI/BiOCOOH p-n heterojunctions were fabricated via a controlled in situ anion-exchange process. During the process, BiOI formation and even deposition on BiOCOOH microspheres with tight interfacial contact were realized. As expected, BiOI/BiOCOOH heterojunctions revealed remarkable enhancements in photocatalytic antibiotic degradation capacities under visible light irradiation compared with pristine BiOI and BiOCOOH. The best-performing BiOI/BiOCOOH heterojunction (i.e., IBOCH-2) showed much improved photocatalytic CIP degradation efficiency of approximately 81- and 3.9-fold greater than those of bare BiOI and BiOCOOH, respectively. The eminent photocatalytic performances were due not only to the enhanced capability in harvesting photon energies in visible light regions, but also the accelerated separation of electrons and holes boosted by the p-n heterojunction. Active species trapping tests demonstrated that superoxide free radicals (•O 2 - ) and photo-generated holes (h + ) were major active species for CIP degradation. Recycling experiments verified the good durability of BIBO-2 over four runs. The facile in situ synthesis route and excellent performance endow flower-like BiOI/BiOCOOH heterojunctions with a promising potential for actual environmental remediation.

Gallium nitride (GaN) is a superior candidate material for fabricating ultraviolet (UV) photodetectors (PDs) by taking advantage of its attractive wide bandgap (3.4 eV) and stable chemical and physical properties. However, the performance of available GaN-based UV PDs (e.g., in terms of detectivity and sensitivity) still require improvement. Fabricating nanoporous GaN (porous-GaN) structures and constructing organic/inorganic hybrids are two effective ways to improve the performance of PDs. In this study, a novel self-powered UV PD was developed by using p -type cobalt phthalocyanine (CoPc) and n -type porous-GaN (CoPc/porous-GaN) to construct a p-n vertical heterojunction via a thermal vapor deposition method. Under 365 nm 0.009 mWcm -2 light illumination, our device showed a photoresponsivity of 588 mA/W, a detectivity of 4.8 × 10 12 Jones, and a linear dynamic range of 79.5 dB, which are better than CoPc- and flat-GaN (CoPc/flat-GaN)-based PDs. The high performance was mainly attributed to the built-in electric field (BEF) generated at the interface of the CoPc film and the nanoporous-GaN, as well as the nanoporous structure of GaN, which allows for a higher absorptivity of light. Furthermore, the device showed excellent stability, as its photoelectrical property and on/off switching behavior remained the same, even after 3 months.

Metal oxide p - n heterojunction nanofibers (NFs) are among the most promising approaches to enhancing the efficiency of gas sensors. In this paper, we report the preparation of a series of p -NiO-loaded n -ZnO NFs, namely (1-x)ZnO-xNiO (x = 0.03, 0.05, 0.7, 0.1, and 0.15 wt%), for hydrogen gas sensing experiments. Samples were prepared through the electrospinning technique followed by a calcination process. The sensing experiments showed that the sample with 0.05 wt% NiO loading resulted in the highest sensing performance at an optimal sensing temperature of 200 °C. The sensing mechanism is discussed in detail and contributions of the p - n heterojunctions, metallization of ZnO and catalytic effect of NiO on the sensing enhancements of an optimized gas sensor are analyzed. This study demonstrates the possibility of fabricating high-performance H₂ sensors through the optimization of p -type metal oxide loading on the surfaces of n -type metal oxides.