Ultra-Sensitive Photo-Induced Hydrogen Gas Sensor Based on Two-Dimensional CeO2-Pd-PDA/rGO Heterojunction Nanocomposite

A two-dimensional (2D) CeO2-Pd-PDA/rGO heterojunction nanocomposite has been synthesised via an environmentally friendly, energy efficient, and facile wet chemical procedure and examined for hydrogen (H2) gas sensing application for the first time. The H2 gas sensing performance of the developed conductometric sensor has been extensively investigated under different operational conditions, including working temperature up to 200 °C, UV illumination, H2 concentrations from 50–6000 ppm, and relative humidity up to 30% RH. The developed ceria-based nanocomposite sensor was functional at a relatively low working temperature (100 °C), and its sensing properties were improved under UV illumination (365 nm). The sensor’s response towards 6000 ppm H2 was drastically enhanced in a humid environment (15% RH), from 172% to 416%. Under optimised conditions, this highly sensitive and selective H2 sensor enabled the detection of H2 molecules down to 50 ppm experimentally. The sensing enhancement mechanisms of the developed sensor were explained in detail. The available 4f electrons and oxygen vacancies on the ceria surface make it a promising material for H2 sensing applications. Moreover, based on the material characterisation results, highly reactive oxidant species on the sensor surface formed the electron–hole pairs, facilitated oxygen mobility, and enhanced the H2 sensing performance.


Introduction
Amongst all the clean energy sources, hydrogen (H 2 ) is an alternative renewable source used in the carbon-neutral hydrogen technologies that can replace traditional energy sources, such as fossil fuels, to avoid carbon emissions, air pollution, and climate change [1]. Therefore, due to the growing economic demand and energy consumption, H 2 is now being used in different industries to produce green energy and power for mobile and stationary applications [1,2]. Across the H 2 supply chain-from generation, transportation, storage, and ultimate use-care must be taken to ensure the safe handling of this volatile fuel [3]. H 2 gas is lighter than air and tends to accumulate in enclosed spaces from even small leaks. Its broad explosive range (4 to 75%), minimal ignition energy (0.017 mJ), and near colourless flame present significant hazards even under a small-scale leakage [4]. Thus, there is a critical need for the subsequent development of H 2 sensing and measurement techniques that are accurate, robust, real-time, power efficient, and scalable for deployment over large spatial scales to accommodate critical data for safe, effective, and efficient H 2 production, storage, and usage [1]. Many semiconducting materials are used for conductometric H 2 sensing, including graphene-based materials, transition metal dichalcogenides, and metal oxides [5,6]. Many different sensing technologies have been developed for H 2 sensing [7][8][9] tal results confirm the potential application of 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite as a high-performance H 2 gas sensing device.

Material Synthesis Procedure and Gas Sensor Fabrication
Commercially produced graphene oxide (GO) powder was obtained from JCNano Inc. Advanced Materials Supplier, Nanjing, China, and the 2D cerium oxide (CeO 2 ) dispersion was purchased from 2D Semiconductors Inc. (Scottsdale, AZ, USA); the concentration was 0.15 mg/mL and the size was less than 100 nm. All the other materials used for the synthesis of CeO 2 -Pd-PDA/rGO heterojunction nanocomposite, (dopamine hydrochloride (DA), palladium (II) chloride (PdCl 2 ), and sodium borohydride (NaBH 4 )), were bought from Sigma-Aldrich, NSW, Australia. Figure 1 demonstrates the schematic diagram of an environmentally friendly and facile synthesis technique for the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite [31,33]. At the start, the GO NSs (10 mg) were mixed in 30 mL of Tris buffer (pH 8.5) and sonicated for 1 h. Then, 10 mg of DA was added to the suspension and sonication was continued until DA was fully dissolved. Later, the mixture was put under vigorous shaking conditions for 24 h. The GO was reduced and functionalised with polydopamine (PDA) through these steps via the self-polymerisation process. The DA initiates self-polymerisation to form polydopamine (PDA) in the presence of GO oxygen functional groups in a weak alkaline environment, with the catechol groups undergoing oxidation until producing the quinone groups, resulting in the reduction of GO [31,33]. the developed sensor is also functional at room temperature (30 °C). The synthesis technique, material characterisation, and H2 sensing mechanisms of the developed 2D CeO2-Pd-PDA/rGO heterojunction nanocomposite are fully explained. The experimental results confirm the potential application of 2D CeO2-Pd-PDA/rGO heterojunction nanocomposite as a high-performance H2 gas sensing device.

Material Synthesis Procedure and Gas Sensor Fabrication
Commercially produced graphene oxide (GO) powder was obtained from JCNano Inc. Advanced Materials Supplier, Nanjing, China, and the 2D cerium oxide (CeO2) dispersion was purchased from 2D Semiconductors Inc. (Scottsdale, AZ, USA); the concentration was 0.15 mg/mL and the size was less than 100 nm. All the other materials used for the synthesis of CeO2-Pd-PDA/rGO heterojunction nanocomposite, (dopamine hydrochloride (DA), palladium (II) chloride (PdCl2), and sodium borohydride (NaBH4)), were bought from Sigma-Aldrich, NSW, Australia. Figure 1 demonstrates the schematic diagram of an environmentally friendly and facile synthesis technique for the CeO2-Pd-PDA/rGO heterojunction nanocomposite [31,33]. At the start, the GO NSs (10 mg) were mixed in 30 mL of Tris buffer (pH 8.5) and sonicated for 1 h. Then, 10 mg of DA was added to the suspension and sonication was continued until DA was fully dissolved. Later, the mixture was put under vigorous shaking conditions for 24 h. The GO was reduced and functionalised with polydopamine (PDA) through these steps via the self-polymerisation process. The DA initiates self-polymerisation to form polydopamine (PDA) in the presence of GO oxygen functional groups in a weak alkaline environment, with the catechol groups undergoing oxidation until producing the quinone groups, resulting in the reduction of GO [31,33]. Afterwards, the synthesised PDA/rGO nanocomposite was sonicated, centrifuged, and washed several times with deionised water (DI). Then, DI water (3 mL) and 1 mL of PdCl2 solution (5 mg/mL) were added to 1 mL of PDA/rGO (1 mg/mL) and mixed for 2 h. Next, 1 mL of freshly made NaBH4 solution (0.5 M) was added to the mixture and stirred for 5 h. The mixture was then centrifuged and washed 3 times with DI water in order to collect the final product, the Pd-PDA/rGO nanocomposite [33]. Then, 0.5 mL of DI was added to the Pd-PDA/rGO nanocomposite powder to form a homogeneous suspension. Afterwards, 1 µL of Pd-PDA/rGO dispersion (1 mg/mL) was drop-casted onto 10 × 6 mm gold interdigitated electrode fingers with a spacing of ~10 µm as a first layer of the sensor. Finally, 1 µL of CeO2 (0.15 mg/mL) dispersion was drop-casted on top of the Pd-PDA/rGO as the second layer to make the CeO2-Pd-PDA/rGO heterojunction nanocomposite sensor device. Afterwards, the synthesised PDA/rGO nanocomposite was sonicated, centrifuged, and washed several times with deionised water (DI). Then, DI water (3 mL) and 1 mL of PdCl 2 solution (5 mg/mL) were added to 1 mL of PDA/rGO (1 mg/mL) and mixed for 2 h. Next, 1 mL of freshly made NaBH 4 solution (0.5 M) was added to the mixture and stirred for 5 h. The mixture was then centrifuged and washed 3 times with DI water in order to collect the final product, the Pd-PDA/rGO nanocomposite [33]. Then, 0.5 mL of DI was added to the Pd-PDA/rGO nanocomposite powder to form a homogeneous suspension. Afterwards, 1 µL of Pd-PDA/rGO dispersion (1 mg/mL) was drop-casted onto 10 × 6 mm gold interdigitated electrode fingers with a spacing of~10 µm as a first layer of the sensor. Finally, 1 µL of CeO 2 (0.15 mg/mL) dispersion was drop-casted on top of the Pd-PDA/rGO as the second layer to make the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite sensor device.

Material Surface Characterisation
The structural and morphological characteristics of the CeO 2 -Pd-PDA/rGO nanocomposite were analysed using different techniques. The scanning electron microscope (EBL-SEM) (Raith150 Two, Raith Germany Co., Ltd., Dortmund, Germany), the high-resolution transmission electron microscope (HRTEM) JEOL ARM200F' NeoARM' (JEOL Ltd., Tokyo, Japan) at 200 kV, and energy-dispersive X-ray spectroscope (EDS) (TESCAN MIRA3 FEG-SEM combined with Thermo Scientific UltraDry EDS, ThermoFisher Scientific, Melbourne, VIC, Australia) were used to investigate the surface morphology and elemental composition of the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite. An X-ray diffractometer (D8-Advanced, Bruker Corporation, Bremen, Germany) with Cu K α and λ = 1.54 Å at 40 kV and 20 mA over the range of 5-95 degrees was applied to determine the crystal phases of the material. Raman spectroscopy (Renishaw plc, Gloucestershire, UK), using 514.5 nm laser excitation, was utilised to measure the Raman spectra of the material.

Gas Sensing Measurements
A gas sensing system [16] was used to examine the gas sensing properties of the conductometric CeO 2 -Pd-PDA/rGO heterojunction nanocomposite-based sensor under different operational conditions. The utilised gas sensing system consists of various parts, including six mass flow controllers (GE50A MFCs) for the regulation of the gas concentrations, temperature and humidity-controlled Linkam stage (T96, Linkam Scientific Instruments Ltd. Tadworth, UK), a built-in heater (LNP96), a Keithly Piccoammeter (model 6487) to periodically measure interval currents throughout the experiments, a humidity generator, and a UV LED (365 nm, M365D1 LED, with 8.9 µW/mm 2 power-driven with a current of 700 mA), which was installed on top of the Linkam stage. The sensor was tested under different working conditions, including temperatures from RT (30 • C) up to 200 • C, relative humidity from 0 to~30% RH at 100 • C, and H 2 concentration from 50 to 6000 ppm. Before each experiment, the sensors were left in pure air for 1 h before the gas exposure. The air/gas mixture flow rate was set at 200 sccm and the target gas exposure time for each experiment was 15 min, followed by two hours of purging for the recovery. For the experiments in the humid condition, the humidity was introduced to the system from the beginning of the experiments and settled for 1 h before gas exposure. The long-term stability and gas selectivity of the sensor were also investigated. The sensor was exposed to 50 ppm of various gases, including hydrogen, nitrogen dioxide, methane, ammonia, and acetone. A bias voltage of 1 V was applied throughout the experiments, and the resistivity change in the sensor was measured upon exposure to the target gas. The response of the sensor (R) was calculated towards the target gas as follows [52][53][54]: where R a is the sensor's resistivity in air and R g is the sensor's resistivity in contact with the target gas. The response and recovery times were calculated when the sensor reached 90% of its response and recovery (back to its initial baseline). Three similar sensors were fabricated for this work, and their gas sensing performance was evaluated. Each experiment was repeated at least three times under the exact operating conditions to validate the reliability and repeatability of the gas sensing process. The gas sensing results of all prepared sensors were comparable.

Material Characterisation Analysis
The morphology and surface structure of the 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite have been analysed by SEM at different magnifications, as shown in Figure 2. The SEM images show the homogeneous distribution of Pd NPs with an average crystalline size of <13 nm and small nanoclusters and the heterogeneous distribution of 2D ceria nanoclusters. When the particle size is small, the surface area increases, resulting in the presence of more active atoms on the surface and consequently more oxygen vacancies accompanied by lattice strain [55]. The lattice parameter is higher for the smaller particle size of CeO 2 due to the higher concentration of oxygen vacancies and their associated Ce 3+ for ceria particles [55]. The porous and multi-layered structure of the PDA functionalised rGO can be seen, which confirms the PDA/rGO NSs are interconnected with some folded 2D ceria nanoclusters. When the particle size is small, the surface area increases, resulting in the presence of more active atoms on the surface and consequently more oxygen vacancies accompanied by lattice strain [55]. The lattice parameter is higher for the smaller particle size of CeO2 due to the higher concentration of oxygen vacancies and their associated Ce 3+ for ceria particles [55]. The porous and multi-layered structure of the PDA functionalised rGO can be seen, which confirms the PDA/rGO NSs are interconnected with some folded edges. Moreover, Figure 2b,c indicate that the PDA/rGO NSs are wrinkled and crumpled, showing the good distribution of the Pd NPs and ceria on both sides of the PDA/rGO NSs and the absence of significant agglomerations.   Elemental composition and surface coverage of the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite were investigated using EDS and presented in Figure 3. The EDS spectrum ( Figure 3f) confirms that the sample (drop-casted on Si substrate) is composed of five elements of carbon, oxygen, palladium, cerium, and Si (substrate). In addition, Figure 3b 2D ceria nanoclusters. When the particle size is small, the surface area increases, resulting in the presence of more active atoms on the surface and consequently more oxygen vacancies accompanied by lattice strain [55]. The lattice parameter is higher for the smaller particle size of CeO2 due to the higher concentration of oxygen vacancies and their associated Ce 3+ for ceria particles [55]. The porous and multi-layered structure of the PDA functionalised rGO can be seen, which confirms the PDA/rGO NSs are interconnected with some folded edges. Moreover, Figure 2b,c indicate that the PDA/rGO NSs are wrinkled and crumpled, showing the good distribution of the Pd NPs and ceria on both sides of the PDA/rGO NSs and the absence of significant agglomerations.   The XRD analysis of the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite is shown in Figure 4 to signify its degree of crystallinity. The XRD profile confirmed a relatively broad peak at 2θ = 27.3 • corresponding to the (002) graphitic plane of the partially restacked rGO NSs with the intralayer spacing of 0.326 nm between the rGO NSs, calculated from Bragg's law (2), as shown below: λ = 2dsin(θ) (2) where the λ (equals 0.154 nm) is the X-ray beam wavelength, θ is the diffraction angle, and d is the intralayer spacing between the rGO NSs. Subsequently, the Scherrer Equation (3) was used to calculate the graphene layers number in rGO NSs to be less than three layers, as follows: where the X is the number of rGO layers, K is a dimensionless shape factor, λ is the X-ray beam wavelength, β is the line broadening at half the maximum intensity (FWHM), and θ is the Bragg angle. The XRD analysis of the CeO2-Pd-PDA/rGO heterojunction nanocomposite is shown in Figure 4 to signify its degree of crystallinity. The XRD profile confirmed a relatively broad peak at 2θ = 27.3° corresponding to the (002) graphitic plane of the partially restacked rGO NSs with the intralayer spacing of 0.326 nm between the rGO NSs, calculated from Bragg's law (2), as shown below: Where the λ (equals 0.154 nm) is the X-ray beam wavelength, θ is the diffraction angle, and d is the intralayer spacing between the rGO NSs. Subsequently, the Scherrer equation (3) was used to calculate the graphene layers number in rGO NSs to be less than three layers, as follows: where the X is the number of rGO layers, K is a dimensionless shape factor, λ is the Xray beam wavelength, β is the line broadening at half the maximum intensity (FWHM), and θ is the Bragg angle.  [33]. Hydrogen adsorption selectivity of the sensing material is highly correlated to the morphology-dependent oxygen reducibility and oxygen vacancy concentrations [56]. Given that, different morphologies of CeO2 possess unique catalytic behaviour corresponding to the specific surface characteristics of each particular lattice plane [57,58]. For instance, the  [33]. Hydrogen adsorption selectivity of the sensing material is highly correlated to the morphologydependent oxygen reducibility and oxygen vacancy concentrations [56]. Given that, different morphologies of CeO 2 possess unique catalytic behaviour corresponding to the specific surface characteristics of each particular lattice plane [57,58]. For instance, the predominant (111) crystal plane is responsible for the selective hydrogenation reaction due to the lowest surface energy and highest oxygen vacancy concentration [59]. In addition, the H 2 molecules occupying the oxygen vacancies on the sensor's surface can improve the photocatalytic activity of the material due to the enhanced optical absorption and the bandgap states [48,60].
Raman analysis of the 2D ceria, Pd-PDA/rGO, and CeO 2 -Pd-PDA/rGO heterojunction nanocomposite was carried out using a 514 nm laser spectrometer and presented in Figure 5.
Raman spectroscopy provides information about the structural transformation of the material and can detect the formation of defects inside the material. Generally, the oxygen vacancies on the surface of ceria are produced due to the reversible reduction of Ce 4+ to Ce 3+ , based on the defect chemistry [61]. The concentration of oxygen vacancy is a critical element in the gas sensing characteristics of the ceria. As shown in Figure 5, the Raman spectrum of CeO 2 shows a sharp peak at~465 cm −1 corresponding to the F 2g mode of symmetric Ce-O 8 stretching vibration in the O h group, which is sensitive to any disorder in the oxygen sublattice [62]. It can be considered a symmetric breathing mode of six oxygen atoms around the central cerium ion. The results confirm the hexagonal shape of the ceria, which is consistent with the TEM results. A small peak at~265 cm −1 can be ascribed to the second-order transverse acoustic mode (2TA). 2D bands can be seen near~2769 cm −1 and~2969 cm −1 , which are slightly shifted to higher wavenumbers in comparison with the 2D band of the Pd-PDA/rGO and CeO 2 -Pd-PDA/rGO heterojunction nanocomposite (~2730 cm −1 and~2923 cm −1 ) due to the layer thickness increase [63]. The Raman spectrum of the Pd-PDA/rGO shows two characteristic peaks at~1355 cm −1 and 1605 cm −1 ascribed to the D and G bands, while the D and G bands of CeO 2 -Pd-PDA/rGO are slightly shifted to the lower wavenumbers (~1352 cm −1 and 1601 cm −1 ), due to the formation of heterojunction between the ceria and Pd-PDA/rGO, and charge transfer [64]. The presence of D and G bands in two spectra also confirms that the Pd-PDA/rGO NSs structure has been maintained after combining with ceria. The D band is correlated with the density of defects in the sp 2 material, and the G band corresponds to the active E 2g phonon mode of the graphite's symmetric structure [65,66]. However, the intensity of the D and G bands of the composite material is downshifted due to the electron transfer from the ceria to rGO NSs, confirming the formation of heterojunctions between ceria and Pd-PDA/rGO NSs, which is consistent with the TEM results [64]. The comparison of the Raman spectra of the pure ceria and CeO 2 -Pd-PDA/rGO nanocomposite reveals that the F 2g mode (Ce-O 8 vibration unit) is shifted to the lower wavenumber (~446 cm −1 ) due to the strong interaction between the ceria Pd-PDA/rGO NSs forming the structural defects, such as oxygen vacancies, which facilitate the charge transfer from the ceria to the rGO NSs [67]. The 2D bands are broadened for the nanocomposite, indicating exfoliation of the rGO [67]. In addition, the Raman spectrum of the nanocomposite confirms that the ceria is successfully incorporated into the Pd-PDA/rGO NSs. The defect density on the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite and Pd-PDA/rGO NSs can be calculated by the intensity ratio (I D /I G ) of the D band to G band, which is increased by loading the ceria to the Pd-PDA/rGO NSs. The I D /I G for Pd-PDA/rGO NSs and CeO 2 -Pd-PDA/rGO nanocomposite were found to be 0.99 and 1.1, respectively, which reflects the higher defect density in the nanocomposite and greater oxygen vacancies on the nanocomposite surface.
Crystal structural features and internal morphology of 2D CeO 2 and CeO 2 -Pd-PDA/rGO heterojunction nanocomposite were investigated by HRTEM, as shown in Figure 6.  (222), and Pd (311) lattice planes, respectively. According to Bragg's law (Equation (2)), the XRD pattern of the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite is consistent with the obtained crystal structural features by HRTEM. As shown in Figure 6c,d, the PDA/rGO NSs are relatively thin layers that help to support the Pd NPs and nanoclusters and 2D CeO 2 to form the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite.  Figure 6c,d demonstrates a few layers of transparent and thin film-like structure of the PDA-rGO NSs decorated with the Pd NPs and 2D CeO2. It can be seen that the Pd NPs are uniformly dispersed onto PDA/rGO NSs surface with a nearly spherical shape, and CeO2 is heterogeneously dispersed into PDA/rGO NSs with some agglomerations. These images prove that the distribution and morphology of the 2D CeO2 and Pd NPs into the

H 2 Gas Sensing Description
The effect of different operating conditions, including H 2 concentration (50-6000 ppm), working temperature (30-200 • C), UV (365 nm) illumination, and relative humidity (up to 30% RH) on the H 2 sensing performance of the 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite sensor was investigated, respectively, and reported in the following sections. that help to support the Pd NPs and nanoclusters and 2D CeO2 to form the CeO2-Pd-PDA/rGO heterojunction nanocomposite.

H2 Gas Sensing Description
The effect of different operating conditions, including H2 concentration (50-6000 ppm), working temperature (30-200 °C), UV (365 nm) illumination, and relative humidity (up to 30% RH) on the H2 sensing performance of the 2D CeO2-Pd-PDA/rGO heterojunction nanocomposite sensor was investigated, respectively, and reported in the following sections.

Effect of Operating Temperature on the H2 Sensing Performance
The gas sensing properties of semiconductor sensors are greatly dependent on the operating temperature due to the direct relation with their chemo-resistive adsorptiondesorption behaviour and, more importantly, the association with power consumption

Effect of Operating Temperature on the H 2 Sensing Performance
The gas sensing properties of semiconductor sensors are greatly dependent on the operating temperature due to the direct relation with their chemo-resistive adsorptiondesorption behaviour and, more importantly, the association with power consumption and cost of experiment [68]. Therefore, to optimise the operating temperature as a key element in gas sensing valuation, the dynamic response of the fabricated CeO 2 -Pd-PDA/rGO sensor towards H 2 with different concentrations (200-600 ppm) was examined at different working temperatures (30 • C up to 200 • C) and 0% relative humidity (% RH) in the dark environment ( Figure 7). As shown in Figure 7, the CeO 2 -Pd-PDA/rGO sensor behaves as a p-type semiconductor, where its resistivity increases upon exposure to H 2 (reducing gas) due to the charge transfer from the target gas molecules to the sensing layer [3]. The electrons move from H 2 , as an electron donor gas, to the valence band of the CeO 2 -Pd-PDA/rGO nanocomposite, which reduces the hole concentration on the surface and, as a result, its conductivity.
at different working temperatures (30 °C up to 200 °C) and 0% relative humidity (% RH) in the dark environment ( Figure 7). As shown in Figure 7, the CeO2-Pd-PDA/rGO sensor behaves as a p-type semiconductor, where its resistivity increases upon exposure to H2 (reducing gas) due to the charge transfer from the target gas molecules to the sensing layer [3]. The electrons move from H2, as an electron donor gas, to the valence band of the CeO2-Pd-PDA/rGO nanocomposite, which reduces the hole concentration on the surface and, as a result, its conductivity. The 2D CeO2-Pd-PDA/rGO heterojunction nanocomposite-based sensor has shown promising H2 sensing responses at low operating temperatures in dark conditions, as shown in Table 1. However, a baseline drift happens due to partly irreversible gas/material chemisorption, indicating that the sensor is not fully recovered to its baseline. This is resolved by introducing UV radiation and changing the charge carrier density on the surface of the CeO2-Pd-PDA/rGO by stimulating the electrons from the valence band.  The 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite-based sensor has shown promising H 2 sensing responses at low operating temperatures in dark conditions, as shown in Table 1. However, a baseline drift happens due to partly irreversible gas/material chemisorption, indicating that the sensor is not fully recovered to its baseline. This is resolved by introducing UV radiation and changing the charge carrier density on the surface of the CeO 2 -Pd-PDA/rGO by stimulating the electrons from the valence band. The change in resistivity of the sensor upon exposure to H 2 gas at different concentrations was measured throughout the experiment. Based on the acceleration of the adsorption/desorption kinetics between the CeO 2 -Pd-PDA/rGO nanocomposite and H 2 molecules, the sensor's responses were enhanced by increasing the operating temperature from 30 • C up to 100 • C [6,69,70]. The maximum sensor response at 600 ppm H 2 was 114% at 100 • C; thus, the 100 • C was chosen as the optimum working temperature. By further increasing the operating temperature above 100 • C, the sensing responses gradually reduced due to the Langmuir effect, where the desorption rate of H 2 molecules exceeds its adsorption rate on the surface of the CeO 2 -Pd-PDA/rGO nanocomposite [57]. In addition, by increasing the temperature beyond the optimum, the adsorbed H 2 molecules on the CeO 2 -Pd-PDA/rGO nanocomposite surface might escape before the charge transfer due to the high activation, resulting in a poor response [71].

Effect of UV Radiation on the H 2 Sensing Performance
The UV radiance effect on H 2 sensing performance of the 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite-based sensor was investigated at 100 • C and 0% RH as a function of H 2 concentration. Figure 8 compares the dynamic response of the sensor upon exposure to H 2 with different concentrations (200-600 ppm) at 100 • C and 0% RH without and with UV (365 nm) illumination. The resistivity change depends on the adsorption/desorption rates of the H 2 molecules onto the CeO 2 -Pd-PDA/rGO sensing layer, which is correlated to the H 2 concentrations [72]. By increasing the gas concentration, the number of gas molecules interacting with the surface of the sensing layer rises until the adsorption and desorption reach a balanced state [73]. Figure 8 compares the dynamic response of the sensor in the dark and under UV illumination, which indicates that the sensor was not fully recovered to its original baseline in the dark. However, the sensor is fully recovered by introducing the UV, and no drift has happened in the baseline. These results reveal that the interaction between the H 2 molecules and the CeO 2 -Pd-PDA/rGO sensing layer under UV radiation is fully reversible [12,74,75].
The change in resistivity of the sensor upon exposure to H2 gas at different concentrations was measured throughout the experiment. Based on the acceleration of the adsorption/desorption kinetics between the CeO2-Pd-PDA/rGO nanocomposite and H2 molecules, the sensor's responses were enhanced by increasing the operating temperature from 30 °C up to 100 °C [6,69,70]. The maximum sensor response at 600 ppm H2 was 114% at 100 °C; thus, the 100 °C was chosen as the optimum working temperature. By further increasing the operating temperature above 100 °C, the sensing responses gradually reduced due to the Langmuir effect, where the desorption rate of H2 molecules exceeds its adsorption rate on the surface of the CeO2-Pd-PDA/rGO nanocomposite [57]. In addition, by increasing the temperature beyond the optimum, the adsorbed H2 molecules on the CeO2-Pd-PDA/rGO nanocomposite surface might escape before the charge transfer due to the high activation, resulting in a poor response [71].

Effect of UV Radiation on the H2 Sensing Performance
The UV radiance effect on H2 sensing performance of the 2D CeO2-Pd-PDA/rGO heterojunction nanocomposite-based sensor was investigated at 100 °C and 0% RH as a function of H2 concentration. Figure 8 compares the dynamic response of the sensor upon exposure to H2 with different concentrations (200-600 ppm) at 100 °C and 0% RH without and with UV (365 nm) illumination. The resistivity change depends on the adsorption/desorption rates of the H2 molecules onto the CeO2-Pd-PDA/rGO sensing layer, which is correlated to the H2 concentrations. [72]. By increasing the gas concentration, the number of gas molecules interacting with the surface of the sensing layer rises until the adsorption and desorption reach a balanced state [73]. Figure 8 compares the dynamic response of the sensor in the dark and under UV illumination, which indicates that the sensor was not fully recovered to its original baseline in the dark. However, the sensor is fully recovered by introducing the UV, and no drift has happened in the baseline. These results reveal that the interaction between the H2 molecules and the CeO2-Pd-PDA/rGO sensing layer under UV radiation is fully reversible [12,74,75].  The UV photoexcitation weakens the bonding forces between the H 2 molecules and CeO 2 -Pd-PDA/rGO nanocomposite sensing layer throughout the physisorption, leading to reversible adsorption/desorption processes [74,76,77]. Moreover, UV illumination stimulates the electrons from the valence band of the CeO 2 -Pd-PDA/rGO surface [78]. It changes the charge carrier density on its surface and consequently accelerates the adsorption of H 2 molecules by these photogenerated electrons from the pre-adsorbed ambient oxygen species [78]. As shown, the oxygen vacancies play a significant role in the photocatalytic activities and adsorption behaviour in semiconducting metal oxides, including CeO 2 , due to the creation of isolated levels below the conduction band [79]. In addition, ceria is a photocatalyst with a 4f electron configuration, which improves its adsorption capacity, especially under UV illumination. When exposed to H 2 as a reducing agent, the electrons transfer into the Ce 4f orbitals and consequently to oxygen, forming superoxide anion radicals [40]. In other words, under UV illumination, highly reactive oxidant species including • OH, HO 2 • , and O 2 •− can be produced on the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite surface, resulting in electron-hole pair formation, i.e., where the electrons are excited from the valence band to the conduction band, leaving holes in the valence band [80]. These photoproduced electron-hole pairs migrate to the surface, giving rise to the reduction reaction of the electron acceptor (O 2 ) to active oxygen ( • O 2 − ) and the holes oxidise H 2 (the electron donor), forming hydroxyl radicals and/or H 2 O. The active • O 2 − and OH • facilitate the oxidisation of the adsorbed H 2 molecules, improving its H 2 sensing performance [81].
The response values of the CeO 2 -Pd-PDA/rGO sensor without and with UV illumination at 100 • C and 0% RH were analysed for each experiment at different H 2 concentrations (200-600 ppm) and reported in Table 2.  Table 2 confirms an enhancement in the H 2 sensing responses of the sensor under UV radiation, which can be attributed to the reduction in the adsorption energy barrier between the H 2 molecules and the photo-induced sensing layer [82]. In addition, the wide bandgap of ceria (3.1 eV) needs UV illumination to enhance its photocatalytic reaction, resulting in increased numbers of oxygen vacancies in the CeO 2 lattice and Ce 3+ ions on the surface [83]. Therefore, increasing the number of H 2 molecules occupying the oxygen vacancies on the sensor's surface improves the sensor's gas sensing activity based on the UV light effect of shifting the ceria's bandgap and accelerating the adsorption rate [48,60]. However, the gas sensing mechanism of the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite based-sensor is complicated and cannot be generalised due to various physical and chemical adsorption/desorption interactions, such as π-π interactions, van der Waals forces, oxygen molecule adsorption/desorption, formation of different chemical bonds, and charge transfer between the H 2 molecules and the sensing layer [70,84].

Relative Humidity Effect on the H 2 Sensing Performance
The above discussed H 2 sensing parameters of the CeO 2 -Pd-PDA/rGO nanocomposite sensor was investigated under dry ambient conditions. One of the critical environmental elements affecting the H 2 sensing parameters is relative humidity (% RH) [85]. Water molecules in humid environments contribute to the adsorption/desorption mechanism, influencing physisorption and chemisorption processes [76,86]. Therefore, we studied the effect of the humid environment, changing from a dry ambient up to 30% RH, on the CeO 2 -Pd-PDA/rGO sensing parameters at different H 2 concentrations and 100 • C. All experiments were performed under UV (365 nm) illumination. Table 3 presents all the calculated H 2 sensing response magnitudes of the CeO 2 -Pd-PDA/rGO sensor towards H 2 concentrations of 4000 and 6000 ppm at different % RH. As indicated in Table 3, the sensor's responses are improved by raising the H 2 concentration from 4000 to 6000 ppm. The sensing mechanism of the p-type CeO 2 -Pd-PDA/rGO heterojunction conductometric sensor is based on ion-sorption of H 2 molecules, followed by a charge transfer directly between the H 2 molecules and heterostructure-based CeO 2 -Pd-PDA/rGO that produces a variation in the Fermi level (i.e., change in the electrical conductivity). The presence of more H 2 molecules on the surface facilitates the electron transfer from the H 2 , as an electron donor gas, to the valence band of the CeO 2 -Pd-PDA/rGO nanocomposite, decreasing the hole concentration on the surface and improving the response. It can also be seen that the response magnitude increases by enriching the % RH up to 15%, which may be due to the participation of water molecules in physical and chemical adsorption/desorption reactions [87]. The water molecules act as electron donors, so by increasing the humidity percentage, the number of adsorbed water molecules increases on the surface, resulting in a narrowing of the depletion region and an increase in the sensor's resistance [87,88]. This reaction leads to an enhancement in gas sensing response for the p-type CeO 2 -Pd-PDA/rGO sensor.
Moreover, carbonyl and hydroxyl functional groups on the CeO 2 -Pd-PDA/rGO nanocomposite surface facilitate its interaction with water molecules, consequently changing the conductivity [89]. On the other hand, the surface-adsorbed active oxygen species play a significant role in the H 2 sensing performance. The interaction between the oxygen species on the CeO 2 -Pd-PDA/rGO surface and adsorbed H 2 molecules can form the hydroxyl active sites, improving the response [90]. Table 3 also reveals that the response magnitude declines by further elevating the humidity up to 30%. With increasing the % RH beyond 15%, the excess water molecules on the surface cause widening of the bandgap by breaking the material sublattice and symmetry (especially the rGO), which leads to a change in conductivity and a reduction in the response [91]. Moreover, in an environment with a high humidity level, the water molecules cannot be readily adsorbed on the surface of the sensing layer because the size of water molecules is greater than H 2 molecules [85]. Therefore, the response of the sensor decreases. Table 4 compares the calculated H 2 sensing parameters of the CeO 2 -Pd-PDA/rGO sensor, including response magnitude and response and recovery times towards H 2 with various concentrations at 0 and 15% RH. It can be seen that by raising the H 2 concentration, the response of the sensor increases, which can be attributed to the increased number of H 2 molecules interacting with the sensor, enhancing its adsorption rate on the surface of the sensing layer. This continues until the sensor becomes saturated and the adsorption and desorption rate reach a balance.
As shown in Table 4, the maximum response of the CeO 2 -Pd-PDA/rGO sensor was 172% in dry ambient conditions towards 6000 ppm H 2 at 100 • C under UV radiation. However, the sensor response drastically improved, to 416%, by raising the humidity to 15% RH under the same operational conditions. This can be attributed to the competition between the H 2 and water molecules to be adsorbed on the sensing layer's surface [75,92]. The H 2 O molecules participate in the adsorption process in the humid environment, influencing the chemisorption and physisorption sensing mechanisms [6,76,92]. In addition, the high response of the sensor and its sensing improvement in a humid environment can be due to the hydroxylation reaction of the water molecules and the reaction between the hydrogen and oxygen ions (O 2− (ads) and O − (ads) ) on the sensing layer surface [93]. Table 4 also reveals that response and recovery times of the sensor were improved by introducing 15% RH. Quick response and recovery of 70 s and 180 s were observed when the sensor was exposed to 6000 ppm H 2 at 100 • C and 15% RH under UV due to the high permeability of the CeO 2 -Pd-PDA/rGO sensor to water molecules. Figure 9a demonstrates the dynamic response of the sensor at 0% and 15% RH at H 2 with different concentrations and 100 • C. Figure 9b,c compares the response and recovery times trends while increasing the humidity and H 2 concentrations.
creases, which can be attributed to the increased number of H2 molecules interacting with the sensor, enhancing its adsorption rate on the surface of the sensing layer. This continues until the sensor becomes saturated and the adsorption and desorption rate reach a balance.
As shown in Table 4, the maximum response of the CeO2-Pd-PDA/rGO sensor was 172% in dry ambient conditions towards 6000 ppm H2 at 100 °C under UV radiation. However, the sensor response drastically improved, to 416%, by raising the humidity to 15% RH under the same operational conditions. This can be attributed to the competition between the H2 and water molecules to be adsorbed on the sensing layer's surface [75,92]. The H2O molecules participate in the adsorption process in the humid environment, influencing the chemisorption and physisorption sensing mechanisms [6,76,92]. In addition, the high response of the sensor and its sensing improvement in a humid environment can be due to the hydroxylation reaction of the water molecules and the reaction between the hydrogen and oxygen ions ( ( ) and ( ) ) on the sensing layer surface [93]. Table 4 also reveals that response and recovery times of the sensor were improved by introducing 15% RH. Quick response and recovery of 70 s and 180 s were observed when the sensor was exposed to 6000 ppm H2 at 100 °C and 15% RH under UV due to the high permeability of the CeO2-Pd-PDA/rGO sensor to water molecules. Figure 9a demonstrates the dynamic response of the sensor at 0% and 15% RH at H2 with different concentrations and 100 °C. Figure 9b,c compares the response and recovery times trends while increasing the humidity and H2 concentrations. Comparing these dynamic responses reveals that a slight drift happens when the sensor is functioning at 0% RH, showing that the sensor doesn't fully recover, which affects the response. It could be because of some irreversible chemisorption reactions due to the high number of H2 molecules interacting with the sensing surface at high H2 concentrations. However, when the sensor operated at 15% RH, it is fully recovered to its original baseline after each H2 exposure as a result of the presence of H2O molecules. Comparing these dynamic responses reveals that a slight drift happens when the sensor is functioning at 0% RH, showing that the sensor doesn't fully recover, which affects the response. It could be because of some irreversible chemisorption reactions due to the high number of H 2 molecules interacting with the sensing surface at high H 2 concentrations. However, when the sensor operated at 15% RH, it is fully recovered to its original baseline after each H 2 exposure as a result of the presence of H 2 O molecules.
In a humid environment, the response is improved because of the presence of hydroxyl active sites (as electron donors) on the surface, which enhances the electric charge density by forming the hydronium cations from the ionised H 2 O molecules as in [76,86]: In addition, it is observed that by increasing the H 2 concentration from 2000 to 6000 ppm, the response and recovery become quicker due to an increase in the surface coverage rate, accelerating the adsorption/desorption process of the H 2 molecules [70]. Moreover, the sensor reaches its saturation level quicker when exposed to higher H 2 concentrations. Another critical element affecting the fast response and recovery is the formation of the covalent bonds on the CeO 2 -Pd-PDA/rGO sensing layer because of the participation of the hydroxyl and carbonyl groups in the H 2 physisorption and chemisorption reactions and also their interactions with water molecules on the surface [94]. The H 2 O molecules are known as electron donors, facilitating the ionisation of the OH and COOH functional groups on the sensing layer surface to generate a concentration gradient of protons [22]. This gradient induces the diffusion of the protons to the CeO 2 -Pd-PDA/rGO nanocomposite, carrying the voltage and current in the external circuit that accelerates the response [95,96].

Gas Selectivity and Sensor Stability
Gas selectivity of the CeO 2 -Pd-PDA/rGO sensor was examined at 0% RH and optimum operating temperature of 100 • C and displayed in Figure 10a. The sensor was exposed to 50 ppm of H 2 , nitrogen dioxide (NO 2 ), acetone (C 3 H 6 O), ammonia (NH 3 ), and methane (CH 4 ) for 30 min. It can be seen that the sensor was highly responsive to H 2 in comparison with the other gases. The sensor showed a 136% response to H 2 while indicating a low response towards NH 3 (1.4%), C 3 H 6 O (2.6%), and CH 4 (3.2%). Although the sensor showed a 38% response to NO 2 , it was more selective and responsive to H 2 .
In addition, it is observed that by increasing the H2 concentration from 2000 to 6000 ppm, the response and recovery become quicker due to an increase in the surface coverage rate, accelerating the adsorption/desorption process of the H2 molecules [70]. Moreover, the sensor reaches its saturation level quicker when exposed to higher H2 concentrations. Another critical element affecting the fast response and recovery is the formation of the covalent bonds on the CeO2-Pd-PDA/rGO sensing layer because of the participation of the hydroxyl and carbonyl groups in the H2 physisorption and chemisorption reactions and also their interactions with water molecules on the surface [94]. The H2O molecules are known as electron donors, facilitating the ionisation of the OH and COOH functional groups on the sensing layer surface to generate a concentration gradient of protons [22]. This gradient induces the diffusion of the protons to the CeO2-Pd-PDA/rGO nanocomposite, carrying the voltage and current in the external circuit that accelerates the response [95,96].

Gas Selectivity and Sensor Stability
Gas selectivity of the CeO2-Pd-PDA/rGO sensor was examined at 0% RH and optimum operating temperature of 100 °C and displayed in Figure 10a. The sensor was exposed to 50 ppm of H2, nitrogen dioxide (NO2), acetone (C3H6O), ammonia (NH3), and methane (CH4) for 30 min. It can be seen that the sensor was highly responsive to H2 in comparison with the other gases. The sensor showed a 136% response to H2 while indicating a low response towards NH3 (1.4%), C3H6O (2.6%), and CH4 (3.2%). Although the sensor showed a 38% response to NO2, it was more selective and responsive to H2.  The p-type CeO 2 -Pd-PDA/rGO nanocomposite sensing mechanism is mainly based on the charge transfer from the H 2 gas to the sensing material along with the adsorption/desorption interactions of the H 2 molecules with the oxygen active sites on the surface [34,97,98]. The free electrons on the CeO 2 -Pd-PDA/rGO nanocomposite surface interact with oxygen molecules in the air to produce reactive oxygen species (O 2− , O 2 − , and O − ) ions. These reactive ions interact with the H 2 molecules as an electron donor gas, improving the electron charge transfer to the sensing layer, lowering the hole concentration, and rising resistivity [3,34,99]. As mentioned before, the H 2 adsorption selectivity of the CeO 2 -Pd-PDA/rGO is highly correlated to its morphology due to oxygen vacancy concentrations [56]. Therefore, the presence of the CeO 2 (111) facet facilitates the selective hydrogenation reaction based on its lowest surface energy and highest oxygen vacancy concentration [59]. The CeO 2 -Pd-PDA/rGO sensor was repeatedly tested over seven months at 100 • C and 0% RH towards 6000 ppm H 2 . Figure 10b indicates comparable responses of the sensor over time, confirming its long-term stability and lack of significant degradation.

Discussion and Conclusions
An environmentally friendly wet chemistry procedure was used to synthesise the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite, and its H 2 gas sensing behaviour was thoroughly investigated under different working conditions, including temperature up to 200 • C, H 2 concentration from 50-6000 ppm, UV radiation, and relative humidity up to 30% RH. The fabricated p-type sensor performed rapidly with a maximum response of 172% towards 6000 ppm H 2 at the optimum operating temperature of 100 • C in dry ambient conditions, due to the enhanced number of H 2 molecules interacting with the sensing material, accelerating the adsorption/desorption rate on the surface until a balanced state is reached. The heterostructured CeO 2 -Pd-PDA/rGO nanocomposite also showed an excellent response, of 416%, to 6000 ppm H 2 at 15% RH and 100 • C, with high selectivity compared to other gases. This could be attributed to the high volume to surface area ratio of the hybrid sensing material along with the presence of defects on the surface related to oxygen vacancies, as well as the heterojunction interface between the rGO, Pd NPS, and 2D ceria, which leads to additional reaction sites [100]. The surface physical characteristics of the sensor confirmed a heterogeneous distribution of the 2D CeO 2 and Pd NPs onto the PDA/rGO nanosheets. In addition, the multi-layered porous structure of the CeO 2 -Pd-PDA/rGO nanocomposite improved its H 2 gas sensing characteristics. The sensor efficiently exhibited a high response of 136% at a low concentration (50 ppm) of H 2 .
The gas sensing mechanisms of hybrid nanocomposites are still under debate. Many surface characteristics can influence the gas sensing performance, including the grain size, crystal orientation, surface thickness, and lateral dimension, which require further systematic studies on the hybridisation impact on the material's physical, chemical, and electrical characteristics, consequently improving the sensing properties.
However, for p-type conductometric gas sensors in contact with reducing gas, the primary sensing mechanism is based on molecular adsorption and chemisorption of the oxygen species on the surface followed by a charge transfer from the reducing gas molecules to the heterostructure nanocomposite leading to a change in the Fermi level and electrical resistance [24]. The surface morphology and particle size of the materials also influence the H 2 sensing properties. As mentioned before, the grain size highly affects the activity of the sensing layer and the oxygen vacancies on the surface. When the particle size decreases, the surface area and the available active atoms on the surface increase, i.e., more oxygen vacancies accompanied by lattice strain [55]. When the CeO 2 -Pd-PDA/rGO nanocomposite is exposed to H 2 as a reducing gas, Ce 3+ is generated through the reduction of Ce 4+ by the electron left behind due to oxygen vacancies. Therefore, as the concentration of oxygen vacancies increases, the CeO 2 lattice parameter rises [55]. In addition, hybridising the Pd decorated rGO NSs with ceria in the form of the p-n heterojunction nanocomposite has shown a promising influence on the H 2 sensing performance at a low operating temperature (100 • C) with enhanced sensing properties compared to a Pd-rGO sensor [16] and ceria sensor [39].
Since ceria is an n-type semiconductor with a bandgap of 3.1 eV, the presence of UV light reduces its bandgap and activates its photocatalytic reactions. On the other hand, when ceria is exposed to a reducing gas such as H 2 , it releases oxygen, forming suboxides as follows [40]: CeO 2 + xH 2 ↔ CeO 2−x + xH 2 O + xV (7) where V is an oxygen vacancy. Doping the ceria with noble metals such as Pd can lower the reduction temperature, while generally, the reduction requires high temperatures [101]. Doping the ceria also introduces a lattice strain that weakens Ce-O bonds, which reduces oxygen vacancy formation energy and, consequently, alters oxygen ion diffusion [101].
In addition, a further beneficial effect is the formation of Pd-O-Ce bonds in the interface, which are proposed as the active sites on Pd/CeO 2 where chemisorbed H 2 reacts with lattice oxygen [102,103]. In this process, at the optimum temperature, the PdO/Pd phase transforms to Pd-O-Ce, allowing the Pd NPs to adsorb H 2 at low temperatures [103]. Consequently, there is a synergic effect between ceria and Pd, which helps the reducibility of the Pd at a low temperature due to the formation of active interfacial sites [37]. This synergic effect also benefits the material's durability due to the Pd NPs anchoring to the support with Pd-O-Ce bonds [103]. On the other hand, when the CeO 2 (111) is exposed to H 2 gas, the H atoms sit on top of the O atoms on the surface, forming hydroxyl O-H bonds [104]. The adsorption of H atoms on the ceria surface leads to the reduction of Ce ions based on the electron transfer from the H 1s to Ce 4F orbital [104]. Therefore, the reduced Ce ions can trap the H 2 and increase the response. Hybridising CeO 2 with rGO also affected the sensing performance via the formation of a p-n heterojunction between the rGO and CeO 2 and also the appearance of C-O bonding at the interface between rGO and ceria. In summary, the CeO 2 -Pd-PDA/rGO heterojunction nanocomposite can produce highly reactive oxidant species including • OH, HO 2 • , and O 2 •− under UV illumination, where the electrons are excited from the valence band to the conduction band, leaving holes in the valence band. This results in the formation of photoproduced electron-hole pairs, which can migrate to the surface, giving rise to the reduction reaction by adsorbed H 2 molecules on its surface.
The H 2 adsorption selectivity of the sensing material is highly correlated to the morphology-dependent oxygen reducibility and oxygen vacancy concentrations [56]. Given that, different morphologies of CeO 2 possess unique catalytic behaviour corresponding to the specific surface characteristics of each particular lattice plane [57,58]. For instance, the predominant (111) crystal plane is responsible for the selective hydrogenation reaction due to the lowest surface energy and highest oxygen vacancy concentration [59]. In addition, the H 2 molecules occupying the oxygen vacancies on the sensor's surface can improve the photocatalytic activity of the material due to the enhanced optical adsorption and the bandgap states [48,60].
More importantly, one of the critical parameters influencing the H 2 sensing performance is the adsorption of atmospheric H 2 O molecules as a significant source of interference [17,26]. According to the literature, the effect of humidity on the gas sensing parameters is a complex challenge for most resistive H 2 sensors [17,105,106]. However, fabricating H 2 sensors capable of detecting H 2 in a humid environment is necessary for real-world operating conditions [107]. Therefore, the effect of the % RH on the H 2 sensing performance of the 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite-based sensor was investigated in this study. The response of the sensor was drastically enhanced from 172% to 416% by increasing the humidity to 15% at 6000 ppm H 2 and 100 • C under UV light. The response and recovery times also improved from 90 s to 70 s and 660 s to 180 s, respectively. This result can be ascribed to increasing the charge carriers on the sensing layer surface by enriching the % RH because of the adsorbed ionised water molecules. Water is known as a reducing agent and transfers electrons to the sensing layer. In a humid environment, the following reactions can happen:  As shown in Table 5, the H 2 gas sensing parameters of the developed 2D CeO 2 -Pd-PDA/rGO nanocomposite-based sensor are more promising in comparison with the reviewed literature, including pure ceria, Pd-rGO, and metal oxide-doped rGO sensors. Based on the experimental results, reducing the GO by adding the DA, as an environmentally friendly chemical, considerably improved its reduction process, affecting the sensing performance. Moreover, hybridising the PDA/rGO with Pd NPs and 2D CeO 2 suggestively enhanced the H 2 sensing parameters [23]. Last, but not least, the fabricated 2D CeO 2 -Pd-PDA/rGO heterojunction nanocomposite was highly selective to H 2 and displayed acceptable durability over seven months, as well as a very high response and quick response and recovery, and ability to function at low operating temperature.  Acknowledgments: The views expressed herein are not necessarily the views of the Australian Government, and the Australian Government does not accept responsibility for any information or advice contained herein. The authors would like to thank Jamie Riches for assistance in obtaining TEM images at the Central Analytical Research Facility (CARF) at QUT. We would like to acknowledge Christopher Harrison and Andrew Moore for their support in developing the gas sensing system at Swinburne.