key: cord-0907092-ud5d6fjs
authors: Lei, Yanhua; Huo, Da; Ding, Mengchao; Zhang, Fei; Yu, Ruixuan; Zhang, Yuliang; Du, Hailiang
title: Synthesis of Hollow N,P-Doped Carbon/Co(2)P(2)O(7) Nanotubular Crystals as an Effective Electrocatalyst for the Oxygen Reduction Reaction
date: 2022-02-09
journal: ACS Omega
DOI: 10.1021/acsomega.1c05608
sha: 4ffa0a04794a837e81e93fc8268d06a8aade85dc
doc_id: 907092
cord_uid: ud5d6fjs

[Image: see text] Herein, N,P-rich carbon/carbon/Co(2)P(2)O(7) hollow nanotubes with a multilayered wall structure were successfully fabricated for the ORR electrocatalyst. The hollow tube structure catalysts were obtained by carbonizing Co(2)P(2)O(7)/C coated with the phytate-doped PANI. The Co(2)P(2)O(7)/C was obtained by phosphorylating a basic cobalt carbonate with phytic acid (PA). Onset and positive half-wave potentials were measured at 0.90 and 0.84 V, respectively, with a diffusion-limited current density of 4.58 mA/cm(2). Effect of the thickness of polyaniline (PANI) in the electrocatalyst precursor was also investigated. The specific surface area as well as the content of graphitic N altered as the time of PANI polymerization increased, resulting in remarkably different catalytic activities. This study of hollow nanotube catalysts exhibits efficient noble-metal-free oxygen reduction reaction electrocatalysts for other chemical systems, which will provide abundant electrochemical active centers and sufficient energy.

Scientists are exploring new energy alternatives, such as solar energy and electrochemical energy, to combat environmental pollution and the current energy crisis. 1−3 In various electrochemical energy systems, fuel cells have received a lot of attention due to their high energy conversion efficiency, high specific energy, low environmental impact, and high reliability. Several factors limit the use of fuel cells on a large scale, including the poor reaction kinetics of the oxygen reduction reaction (ORR) on the cathode 4 and the use of noble metal catalysts. 4−6 Thus, to address the scarcity and high cost of noble-metal-based catalysts, nonmetallic electrocatalysts, 7,8 nonprecious metal catalysts, 9−12 and low noble metal catalysts 13, 14 have therefore been investigated and inspected.

Among the various alternatives, transition-metal phosphates are regarded as potential alternatives due to their good electrical conductivity, low price, stable properties, and environmental friendliness. The performance of pyrophosphates of divalent metals with the general formula M 2 P 2 O 7 (M1/4 Co, Ni, etc.) is expected to be a promising material of choice for fuel cells. 15 Heteroatom codoping (for example, boron, nitrogen, phosphorus, sulfur, and others) can considerably improve conductivity and functionality while disrupting the initial conjugated electron coordination environment and even achieve metallicity. 16−20 Taking Co-based materials as examples, most zeolite-imidazole framework (ZIF)-based precursors were used to develop active and nonvolatile bimetallic ZIF-derived catalysts to enhance the performance of oxygen reduction. Wang prepared CS Co@ NC-700 and Co@Co 4 N/MnO-NC catalysts using Zn and Mn bimetallic MOFs as precursors, respectively, which not only enhanced the performance of ORR but also acted on Zn-ion batteries to improve their stability. 21, 22 As one of the Co−P materials, Co 2 P 2 O 7 has superior performance in supercapacitors, magnetism, microwave absorption, and multiphase catalysis. 23, 24 In general, Co 2 P 2 O 7 is mostly used for testing OER mainly stemming from the fact that the valence electron density within the Co center of Co 2 P 2 O 7 decreases significantly when the metal undergoes carbonization. However, the performance of Co 2 P 2 O 7 in ORR catalytic performance was far from expectations. It has been reported that the catalytic performance of catalytic materials can be improved through structural design and composition optimization. Graphene nanocages doped with N,P and Co 2 P 2 O 7 act as Mott−Schottky heterojunction electrocatalysts to enhance their interfacial 25 and thus drive their intrinsic catalytic activity. The resulting N,P-doped carbon layer having a metallic nature not only regulates the overfilling of the Co center, for example, the orbitals occupied by the Co 2 P 2 O 7 nanorods (NRs) as cocatalysts, but also ensures continuous and long-term operation. 26 However, the smart structure design and synthesis of heterojunction-based Co 2 P 2 O 7 and N,P-codoped carbon nanostates for electrocatalysts with enhanced performance are problems that urgently need to be addressed.

Herein, hollow nanotube (HNTs) catalysts of N,P-rich carbon/carbon/Co 2 P 2 O 7 (Co 2 P 2 O 7 /C@N,P−C) were successfully fabricated by combining the advantages of both heteroatom-doped carbon materials and transition-metal phosphides to realize the multifunctionality of the catalyst by carbonizing the PANI-coated Co 2 P 2 O 7 . The effect of PANI amount varying by the polymerization time in the catalyst precursor on the catalytic performance was also investigated. The as-prepared catalysts exhibited a much higher electrocatalytic performance and stability for ORR.

The steps needed for electrocatalyst syntheses are depicted in Figure 1 . Co 2 P 2 O 7 /C nanorods were fabricated first by PAcoated chemical Co(CO 3 ) 0.5 (OH)·0.11H 2 O carbonization. The final N,P-rich carbon-coated Co 2 P 2 O 7 /C catalysts were produced in an in situ reaction through high-temperature carbonization and PANI polymerization.

2.1. Synthesis of Co(CO 3 ) 0.5 (OH)·0.11H 2 O. In 30 mL of deionized water (DI), dissolution of urea (0.0902 g, 1.5 mmol) and Co(NO 3 ) 2 ·6H 2 O (0.1455 g, 0.5 mmol) took place. After 1 h of continuous stirring, the formed light-pink solution was transferred to a stainless steel autoclave composed of poly(tetrafluoroethylene) and placed in an electric oven at 120°C for 12 h. The resulting precipitates were then subjected to centrifugation followed by washing with DI water after cooling, and Co(CO 3 ) 0.5 (OH)·0.11H 2 O was collected as a light-pink solid powder after drying in an oven at 60°C.

2.2. Synthesis of Co 2 P 2 O 7 /C NRs. Co 2 P 2 O 7 /C nanorods were synthesized by dissolving 0.1 g of Co(CO 3 ) 0.5 (OH)· 0.11H 2 O prepared above in 10 mmol/L (50 mL) of PA solution and stirring at 60°C for 1 h. The precipitate was then collected and dried before being annealed in an Ar atmosphere at 800°C for 2 h at a heating rate of 5°C/min from room temperature. The resultant samples were labeled Co 2 P 2 O 7 /C NRs.

2.3. Synthesis of N,P-Rich Carbon-Coated Co 2 P 2 O 7 /C Hollow Nanotubes (HNTs). First, 0.1 g of Co 2 P 2 O 7 /C NRs was placed in a 50 mL PA 10 mM solution in a bilayer flask. The temperature of the flask was cooled to 0−5°C by a recirculating cooling pump. Then, 0.1 mL of aniline monomer was injected into the solution. After that, 0.1 g of ammonium persulfate (APS) as an oxidant was sonicated in 50 mL of a 10 mM PA solution and dropped into the bilayer flask at a constant rate using a constant pressure drop funnel. The polymerization reaction was carried out for 3−5 h at 5°C with constant stirring. The PANI-coated Co 2 P 2 O 7 NR product (PANI-co-Co 2 P 2 O 7 /C) was filtered and rinsed multiple times with DI before drying in a vacuum at 60°C. Subsequently, the PANI-co-Co 2 P 2 O 7 /C was annealed for 2 h at 800°C in an Ar atmosphere at a heating rate of 5°C/min. The resultant N,Prich carbon-coated Co 2 P 2 O 7 /C samples were labeled Co 2 P 2 O 7 /C@N,P−C HNTs. For comparison, the catalyst of PANI-derived N,P-doped carbon was obtained by paralyzing the phytate-doped PANI free from the presence of Co 2 P 2 O 7 at 800°C for 2 h.

Characterizations. An X-ray diffraction (XRD) device of the Bruker D8-advance model was used at 40 mA and 40 kV with a 2θ range of 5−90°to analyze the XRD of the catalysts. The X-ray photon spectra (XPS) were collected using a JPS-9200 instrument supplemented with the radiation of Mg Ka. The Bunko−Keiki M30-TP-M setup was used to perform Raman spectroscopy with a polychromator using YVO 4 532 nm laser for excitation. Investigation of the thermal stability of specimens was carried out through the Perkin Elmer Diamond TG/DTA Lab system's thermogravimetry (TG). The specimens were heated up to 1000°C at the rate of 10°C/min under a constant N 2 flow of 50 mL/min. Transmission electron microscopy (TEM) and scanning electron microscopy (SEM) were performed under the JEOL-2010F and JEOL JSM-6510LA instruments, respectively. The electrical conductivity measurements of the composite particles were performed using an ST2253 digital four-probe resistance tester (Suzhou Jingge Electronics Co., Ltd.) at room temperature.

2.5. Electrochemical Analysis. The electrocatalytic performance of the as-prepared samples was evaluated with cyclic voltammetry (CV) and linear sweep voltammetry (LSV) tests on a Gamry workstation connected with a rotating disc setup. Rotating discs and rotation ring-disk electrodes (RRDEs) (PINE) were used to assess the electrochemical catalytic performance. The electrolyte used in this experiment was 0.1 mol/L KOH solution, and the working electrode was a glassy carbon disc with a diameter of about 5 mm equipped with an electrocatalyst, while the reference and counter electrodes were an Ag/AgCl solution using 0.1 mol/L KOH and a platinum wire, respectively. A two-channel Gamry 1010E constant potential meter was used for the rotating disc ring device. For testing, a cleaned reaction cell was used and the electrolyte was passed through oxygen until oxygen saturation; the working electrode was polished and cleaned, and a drop of catalyst ink was applied. The catalyst ink was composed of 2 mg of catalysts, ethanol (400 μL), and Nafion (25 μL, 5 wt %). The working electrode had 0.2 mg/cm 2 catalyst loading density. Also, the specific tests can be found in a previous work of our group. 27 The catalytic electrode was first activated by CV performed at 0−1.2 V (vs reversible hydrogen electrode (RHE)) at a 50 mV/s scanning rate in an O 2 -saturated 0.1 M KOH solution until a steady curve was observed. LSV was collected in the 0−1.2 V range (vs RHE) at 10 mV/s rate in the O 2 -saturated 0.1 M KOH at 100, 400, 900, 1225, 1600, 2000, 2025, and 2500 rpm. All ORR tests were carried out in the presence of a constant oxygen gas stream.

The way to prepare the RRED electrode is to apply a potential of 0.5 V to the Pt ring electrode. Based on the data obtained by RRED, the number of electrons transferred during ORR, n, and the H 2 O 2 yield are determined by the following equations. where I D and I R are the disk and the ring currents, respectively, and N is the current collection efficiency (equal to 0.37). All of the potential values were measured relative to the Ag/ AgCl potential and were recalculated to the RHE scale using the Nernst equation below i k j j j j j y

3. RESULTS AND DISCUSSION 3.1. Synthesis and Characterization of Co 2 P 2 O 7 /C@ N,P−C HNTs. The hollowed Co 2 P 2 O 7 /C@N,P−C NTs were synthesized through carbonizing the PANI-coated Co 2 P 2 O 7 , and the Co 2 P 2 O 7 was obtained by paralyzing the PAsurrounded Co(CO 3 ) 0.5 (OH)·0.11H 2 O NRs, schematically illustrated in Figure 1 . Specifically, the Co(CO 3 ) 0.5 (OH)· 0.11H 2 O clubs with widths of 100−200 nm were first synthesized from Co(NO 3 ) 2 ·6H 2 O and urea. Then, PA with a high P-content was allowed to coat on the surface of Co(CO 3 ) 0.5 (OH)·0.11H 2 O with the help of electrostatic attraction. Subsequently, the protonated PA will react with Co(CO 3 ) 0.5 (OH)·0.11H 2 O and form the coordination of Co 2+ and phytate (Co-phytate). Co 2 P 2 O 7 /C was achieved after carbonization of phytate/Co(CO 3 ) 0.5 (OH)·0.11H 2 O. Then, PANI was polymerized on the surface of Co 2 P 2 O 7 /C from the PA-containing solution. Finally, hollow-tube-structured Co 2 P 2 O 7 /C@N,P−C catalysts are achieved, after calcination, in which PANI acts as the C,N source, while PA acts as the P source.

Powder XRD was employed to ascertain the sample's crystal structure and phase purity. The XRD outcomes in Figure 2a indicated that the products for the samples with the PA cladding pretreatment and PA cladding treatment followed by PANI were composed of Co 2 P 2 O 7 . Other than the peaks of diffraction related to Co 2 P 2 O 7 (JCPDS No. , no impurities could be found in the XRD pattern. The main diffraction and peaks at 29.6, 30.1, 35.3, 43.7, 49.3 and 58.3°c ould be assigned to the (012), (-3̅ 02), (130), (032), (-424) and (-1̅ 34) facets of the Co 2 P 2 O 7 phase, respectively. Further, as shown in Figure 2a , the intensity of the Co 2 P 2 O 7 /C@N,P− Figure 2 . (a) Patterns of XRD for Co 2 P 2 O 7 /C, Co 2 P 2 O 7 /C@N,P−C, and Co 2 P-Co 2 P 2 O 7 /C@N,P−C. (b) Raman spectra of Co 2 P 2 O 7 /C and Co 2 P 2 O 7 /C@N,P−C.

C diffraction peak is significantly higher than that of Co 2 P 2 O 7 / C after the introduction of the conducting polymer. This indicates that the crystallinity of the nanotubule is improved. However, it is interesting that, when carbonizing the PANI-PAcoated Co-(CO 3 ) 0.5 (OH)·0.11H 2 O without the PA cladding pretreatment, the calcination product was composed of Co 2 P 2 O 7 and Co 2 P. The peaks around 40.7, 43.3, 52, and 54.1°are related to the (121), (211), (130), and (002) crystallographic planes of Co 2 P, respectively (JCPDS No. 54-0413). Further, we adopted the solution of bicarbonization to obtain the hollow-structured Co 2 P 2 O 7 /C@N,P−C NT catalysts. Figure 2b shows Raman spectra of Co 2 P 2 O 7 /C and Co 2 P 2 O 7 /C@N,P−C samples. The symmetric stretching vibrations vs PO 3 were attributed to the weak peak at 1033 cm −1 , while the POP bridge in Co 2 P 2 O 7 was related to the peak at 674 cm −1 , 28 confirming the formation of Co 2 P 2 O 7 . The Raman spectrum of the PANI-coated Co 2 P 2 O 7 /C is provided in Figure S1 , in which the Raman shift at 578 cm −1 was allocated to Co 2 P 2 O 7 and the other peaks were attributed to PANI, confirming the successful coating of PANI on Co 2 P 2 O 7 . After carbonization, as shown in Figure 2b , there are two distinct Raman peaks: the G-band at 1600 cm −1 and the Dband at 1350 cm −1 , 29 exhibiting the coating of carbon layers. The D-band emerges as a result of the vibration of sp 3 hybridized C and is thus typical of a graphitic plane that is somewhat disordered or flawed. The appearance of the G-band is due to the E2g vibrations of sp 2 hybridized C and hence shows the degree of graphitization. 30, 31 The intensity ratio (I D / I G ) of these two peaks is often used to assess the degree of disorder or defects in graphitic materials. 32 Defects will change the charge distribution of the neighboring carbon, which may be favorable for electrochemical reactions. 33−35 The I D /I G of Co 2 P 2 O 7 /C @N,P−C at 1.13 is higher than that of the Co 2 P 2 O 7 /C catalyst (which is 1.05), suggesting a higher defect degree in Co 2 P 2 O 7 /C@N,P−C. As a result, the N-doped carbon coated on Co 2 P 2 O 7 /C has a lattice with several defects and disorders. 36 The surface electronic states and composition of the synthesized catalysts were determined using XPS measurements, and the outcomes are illustrated in Figure 3 . The results showed that Co, P, C, and O elements were present in both the Co 2 P 2 O 7 /C and Co 2 P 2 O 7 /C@N,P−C samples (see Figure  3a ). The phosphorization of the phytate derivatives was successful because of the presence of P elements. The PANI resulted in the presence of N in Co 2 P 2 O 7 /C@N,P−C. Detailed information on the structure and composition of Co 2 P 2 O 7 /C@N,P−C is revealed by the Co 2p, P 2p, N 1s, and C 1s XPS spectra (Figure 3 ). Co 2p 3/2 and Co 2p 1/2 peaks are situated at 781.3 and 797.4 eV, and 786.1 and 802.7 eV, respectively, in the Co 2p spectra of Co 2 P 2 O 7 /C, as depicted in Figure 3b . Compared to the Co 2 P 2 O 7 /C NRs, the corresponding peaks of Co 2 P 2 O 7 /C@N,P−C in the low-energy direction of Co 2p 3/2 and Co 2p 1/2 are shifted slightly (Figure 2b ). This is attributed to the Co electron cloud migration due to the PANI surface-doped nitrogen species' strong electronegativity, which indicates the covalent coupling between Co 2 P 2 O 7 /C and the PANI support. 13−15 There is a close association ACS Omega http://pubs.acs.org/journal/acsodf Article between these two components, making the catalysts more conductive and electrochemically active, which aims to enhance ORR activity. 37, 38 As shown in Figure 3c , the C 1s spectrum of Co 2 P 2 O 7 /C@N,P−C contains four distinct peaks, one for aromatic, aliphatic, and graphitic CC bonds at 284.1 eV, while the peaks at 284.4 and 285.6 eV represent C−C and 

http://pubs.acs.org/journal/acsodf Article C−N bonds, respectively, with one disordered peak at 288.1 eV. During the pyrolysis step, we observed carbon bonds (unsaturated and saturated) in samples, which indicates that PANI graphitization had been successful. In particular, compared to Co 2 P 2 O 7 /C, the C−N bond indicates the successful incorporation of N atoms of PANI into the carbon matrix. 39, 40 The P 2p peak of Co 2 P 2 O 7 /C@N,P−C ( Figure  3d ) demonstrates three peaks at 133.1, 133.9, and 134.9 eV. The first two peaks correspond to the P 2p 3/2 and P 2p 1/2 phosphate group central phosphorus atom nuclear levels, whereas the latter (134.9 eV) is linked to the phosphorus-like bonding to the carbon lattice structure. 41−44 In the P 2p region of Co 2 P 2 O 7 /C, two distinct P species were introduced ( Figure  2d ). The first (133.5 eV) is because of P atoms chemically bound to O atoms, whereas the second (135.2 eV) is due to P−C coordination. The presence of P−O−P and P−C bonding is in agreement with the FTIR study in Figure S2 , in which the vibrations of P−O−P and P−C in the infrared spectrum were attributed to the peaks at 765 and 1076 cm −1 , respectively. 28 The morphology and structure of the synthesized catalysts were then observed with SEM and TEM. The results in Figure  4a −c show that the sample Co 2 P 2 O 7 /C is composed of carbon-coated wrapping nanobars (Co 2 P 2 O 7 ) with a length of over 1 μm and a diameter of approximately 100 nm. However, after the pyrolyzation treatment of the PANI-co-Co 2 P 2 O 7 /C precursor, one-dimensional (1D) hollow nanotube catalysts were observed, as shown in Figure 4d ,e. Interestingly, the hollow tube structure is more remarkably pronounced with an inner diameter of around 100 nm. This hollowed structure is very beneficial to the penetration of the electrolyte and the transfer of electrons/protons during electrocatalysis. Meanwhile, the rough surface added by the carbon shell provides the potential for efficient mass transport and ion diffusion.

The shape and microstructure of the catalysts, as well as the precursors, were further observed with TEM and highresolution TEM (HRTEM). The precursor of Co-(CO 3 ) 0.5 (OH)·0.11H 2 O nanowires (solid) with a diameter of around 100 nm and different lengths of ∼μm can be observed in Figure S3 . Then, after the PA was introduced into the solution of Co (CO 3 ) 0.5 (OH)·0.11H 2 O, PA induced decomposition of Co (CO 3 ) 0.5 (OH)·0.11H 2 O, thus resulting in the coordination of Co 2+ with surface phytate (Co-phytate) with the help of electrostatic attraction. Figure S3c ,d shows that an organic layer covered the porous substrates with a thickness of approximately 10 nm, indicating that PA was successfully covered on the surface of Co(CO 3 ) 0.5 (OH)·0.11H 2 O. Figure  S4 shows the TEM images of Co 2 P 2 O 7 /C, which were obtained by carbonization of the PA-treated Co (CO 3 ) 0.5 (OH)·0.11H 2 O NRs. Interestingly, the rodlike Co 2 P 2 O 7 /C with a carbon shell can be seen in Figure S4 , and further high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and element-mapping images in Figure S4 verify that the C and P elements are distributed around Co 2 P 2 O 7 .

Further, after the carbonization of the PANI-PA-coated Co 2 P 2 O 7 /C, as presented in the low-magnification TEM images in Figure 5a , the feature with hollowed nanotube walls was confirmed. The Co 2 P 2 O 7 nanoparticles are wrapped by the hollowed PANI-derived N, P-doped carbon tube. The Co 2 P 2 O 7 nanoparticles are inserted into the carbon skeleton when we magnify the wall (Figure 5b ). The lattice fringes show that the 0.31 nm interlayer spacing corresponds to the (012) plane of Co 2 P 2 O 7 , which is in agreement with the XRD assessment. The hollow feature is further demonstrated in Figure 5d by the high-angle annular dark-field (HAADF) image and related EDS maps of Co 2 P 2 O 7 @N,P−C with uniform distributions of Co, P, and O elements in the inside and N, C elements in the exterior. These findings contribute to the development of a heterogeneous electrocatalyst comprising Co 2 P 2 O 7 nanoparticles embedded in N,P-codoped tubular carbon. According to previous reports on carbon nanostructures wrapping metal or other inorganic nanoparticle hybrids, the introduced carbon layer can not only "armor" the Co 2 P 2 O 7 cores and prevent them from being destroyed during electrochemical cycling but also enhance electron penetration or tunneling and facilitate electrocatalytic application. N 2 adsorption−desorption tests were employed to assess the specific surface area and porosity of the prepared materials. The BET specific surface area of Co 2 P 2 O 7 /C@N,P−C was found to be 459.3 m 2 /g, which was greater than that of Co 2 P 2 O 7 /C (104.7 m 2 /g, Figure 6 ). The formation of the 1D hollowed tube structure obviously promotes the BET specific surface area. The hierarchical porous structure is noted to have an average pore diameter of 2.63 nm in Co 2 P 2 O 7 /C@N,P−C. Meanwhile, the large pore with the diameter close to 80 nm in the pore distribution curve of Figure 6b mainly corresponded to the inner diameter of the formed hollow Co 2 P 2 O 7 /C@ Figure 6 . (a)Adsorption−desorption isotherms for N 2 for Co 2 P 2 O 7 /C@N,P−C and Co 2 P 2 O 7 /C; (b) pore diameter distribution diagram.

http://pubs.acs.org/journal/acsodf Article N,P−C tubes. The porous carbon derived from the carbonized PANI matrix as well as the 1D hollowed tube structure was responsible for the increased specific surface area. The hierarchical porous structure develops a specific surface area, which provides numerous energetic spots for the catalytic reaction; meanwhile, porosity facilitates the transfer of reactants, promotes the occurrence of catalytic response, and thus improves the catalytic ability. 3.2. Electrochemical Activity of Co 2 P 2 O 7 /C@N,P−C HNTs. To study the electrochemical properties, a three-electrode system was used in an aqueous 0.1 M KOH. The voltage range was 0−0.5 V (relative to RHE). Figure 7a illustrates the curves of CV for Co 2 P 2 O 7 /C, Co 2 P 2 O 7 /C@ N,P−C, PANI-derived N,P−C, and commercial 20% Pt/C at a scan rate of 50 mV/s. The area around the ring of the CV curve for Co 2 P 2 O 7 /C@N,P−C is larger than that of the Co 2 P 2 O 7 /C electrode, exhibiting better capacitive performance. LSV tests of Co 2 P 2 O 7 /C@N,P−C conducted at 1600 rpm exhibited a diffusion-limited current density of 4.6 mA/ cm 2 at 0.2 V (Figure 7c) , which is substantially greater than (c) Curves of RRDE for 20 wt % Pt/C, Co 2 P 2 O 7 /C@N, P−C, Co 2 P 2 O 7 / C, and PANI-derived N,P−C catalysts. Densities of the ring (upper) and disc (bottom) currents observed at 1600 rpm. (d) Calculated electron transfer numbers n for the RRDE data for Co 2 P 2 O 7 /C@N,P−C, Co 2 P 2 O 7 /C, PANI-derived N,P−C, and 20% Pt/C. (e) Half-wave (blue) and onset (green) potentials together with the restricted current density (gray) values for Co 2 P 2 O 7 /C, Co 2 P 2 O 7 /C@N,P−C, Co 2 P-Co 2 P 2 O 7 /C@ N,P−C, PANI-derived N,P−C, and 20% Pt/C catalysts.

http://pubs.acs.org/journal/acsodf Article that of Co 2 P 2 O 7 /C at 2.23 mA/cm 2 and PANI-derived N,P−C at 3.46 cm −2 . A more positive onset potential was observed for Co 2 P 2 O 7 /C @N,P−C (equal to 0.91 V) than that of Co 2 P 2 O 7 /C at 0.6 V and PANI-derived N,P−C at 0.84 V. The half-wave potential of Co 2 P 2 O 7 /C@N,P−C is 0.85 V, and the value is only 50 mV lower than commercial 20 wt % Pt/C catalysts. The ORR pathway was computed, and the OH 2 − ORR yield was screened using RRDE. During ORR with the Co 2 P 2 O 7 /C@N,P−C catalyst, the OH 2 − yield was 1.0% (see Figure 7c ), and the value of n (electron transfer number) was observed in the range of 3.97−3.98, which is quite close to the 20 wt % Pt/C catalyst value. However, the n values and OH 2 − yield attained for the Co 2 P 2 O 7 /C catalyst-assisted ORR were substantially different from those achieved for the reactions assisted by the 20% Pt/C and Co 2 P 2 O 7 /C@N,P−C materials, which demonstrates a four-/two-electron mixed transfer pathway.

In Table 1 , we compare the ORR ability of the lately reported Co 2 P 2 O 7 -based catalyst with our catalysts. Gratifyingly, the catalyst here reported exhibits a superior perform- (c) Curves of RRDE for 20 wt % Pt/C, Co 2 P 2 O 7 /C@N,P−C-3h, Co 2 P 2 O 7 /C@N,P−C-4h, and Co 2 P 2 O 7 /C@N,P−C-5h catalysts. The ring current densities (upper) and disk current densities (bottom) were achieved at 1600 rpm. (d) Evaluated electron transfer numbers n for the RRDE data for Co 2 P 2 O 7 /C@N,P−C-3h, Co 2 P 2 O 7 /C@N,P−C-4h, Co 2 P 2 O 7 /C@N,P−C-5h, and 20% Pt/C.

http://pubs.acs.org/journal/acsodf Article ance no matter the limiting current density and E 1/2 . These findings indicate that the Co 2 P 2 O 7 /C@N,P−C materials exhibit an outstanding ORR catalytic activity, which may result from the special hollow tube nanohybrid structure. A synergetic effect of individual components leads to enhancing the ORR movement. In terms of electrocatalytic performance results (Figure 7b ), the performance of the composite ternary catalyst is much higher than the performance of PANI-derived N,P-doped C and Co 2 P 2 O 7 /C. The Co 2 P 2 O 7 NRs obtained from the Co(CO 3 ) 0.5 (OH)·0.11H 2 O precursors are more likely to serve as templates for the fabrication of N,P−C, instead of taking effect in the ORR process. The promising ORR activities of the Co 2 P 2 O 7 /C@N,P−C catalysts also highlight the advantages of the exposure of more active sites given by the well-defined 1D hollow nanotube structure and the synergetic interactions between Co 2 P 2 O 7 /C and PANIderived N,P−C in favor of the absorption/desorption of the oxygenated species during the electrocatalytic processes. Moreover, the N,P-doped carbon enhances the specific surface area; thus, the resulting abundant pores and open tunnels permit the facile access of O 2 bubbles and electrolytes toward the active sites to accelerate the ORR process. Further, there also is a considerable electronic coupling effect in the Co 2 P 2 O 7 /C and PANI-derived N,P−C components, and electrons can be transferred into the thin C shells from Co 2 P 2 O 7 cores. The conductivity of the catalyst material obtained by four-probe methods was much improved due to the wrapping of PANI-derived N,P−C, with σ Co2P2O7/C = 0.468 S/cm up to σ Co2P2O7/C@N,P-C = 1.87 S/cm. The thin C shells, in other words, can improve the interfacial electron or electron penetration transfer. Additionally, the pyridinic and graphitic nitrogen atoms with their sp 2 electronic structures are very active ORR sites. 8, 45, 46 They enhance the material electronic conductivity and increase the catalyst corrosion resistance, which, again, can effectually advance the movement and constancy of the catalysts. From the above discussion, it is easy to see that the presence of the pyrolytic N,P-doped carbon layer derived from the PANI layer plays an important role in the ORR catalytic performance. A huge improvement of ORR over the original Co 2 P 2 O 7 /C was observed. Thus, the effects of polymerized PANI amounts controlled by the polymerization time on the catalyst performance were then investigated. Figure 8 compares the curves of CV and LSV for Co 2 P 2 O 7 / C@N,P-C with different PANI polymerization times during the synthesis process of their carbonized precursors. A distinct cathodic peak can be observed for all of the Co 2 P 2 O 7 C@N,P− C samples, which corresponds to the featureless CV curves in O 2 -saturated solutions, and the catalytic performance is highly dependent on the quantity of PANI loaded during catalyst preparation. Further, the ORR onset potential of the Co 2 P 2 O 7 / C@N,P−C catalyst significantly shifts negatively, and the oxygen reduction current peak dramatically reduced with the increase in polymerization time of PANI. The Co 2 P 2 O 7 /C@ N,P−C-3h catalyst exhibits the highest overall ORR activity, which is close to that of 20 wt % Pt/C in Figure 8 . LSV curves recorded at 1600 rpm show that Co 2 P 2 O 7 /C@N,P−C-3h has a higher onset potential (E onset ) of 0.90 V vs RHE and a halfwave potential (E 1/2 ) of 0.84 V than that of Co 2 P 2 O 7 /C@ N,P−C-4h and Co 2 P 2 O 7 /C@N,P−C 5h, separately ( Figure  8b ). The polymerization time in the catalyst precursor had a significant influence on the OH 2 − yield and the electron transfer number n attained for the ORR assisted by the Co 2 P 2 O 7 /C@N,P−C catalyst. During ORR with the Co 2 P 2 O 7 /C@N,P−C-3h catalyst, the OH 2 − yield was 1.0% (see Figure 8c) , and the electron transfer number n was in the 3.97−3.98 range, which is extremely similar to the value of the 20 wt % Pt/C catalyst. Moreover, increasing the polymerization duration of PANI in the corresponding precursors resulted in OH 2 − yields and n that were not the same as the ones found in reactions facilitated by 20% Pt/C and Co 2 P 2 O 7 C@N,P−C-3h materials, which suggests a twoelectron transfer pathway. The weaker presentation of the other catalysts prepared with a longer polymerization time could be explained by the formation of the thicker N-doped Figure 9 . XPS High-resolution N 1s spectra for (a) Co 2 P 2 O 7 /C@N,P−C-3h, (b) Co 2 P 2 O 7 /C@N,P−C-4h, and (c) Co 2 P 2 O 7 /C@N,P−C-5h.

http://pubs.acs.org/journal/acsodf Article carbon, which is highly confirmed by the following results of XPS and BET measurements. First, the N1s core-level XPS spectra of the synthesized catalysts were shown in Figure 9 , and four types of N bonds were divided. The composed ratio of the different type N was summarized in Table 2 . Based on the XPS results, it was noticed that the different N species ratios in the catalysts were strongly influenced by the varied polymerization times of PANI in the catalytic precious that leads to the variety of loaded outside N−C thickness after pyrolysis treatment (see Figure 9 and Table 2 ). As shown in Table 2 , as the polymerization time in the precursor of the Co 2 P 2 O 7 /C@ N,P-C catalyst enhanced, the total content of graphite N and pyridine N decreased. Co 2 P 2 O 7 /C@N,P−C-3h has the greatest total content of graphite N and pyridine N, which is 68.15%. It has been shown that pyridine nitrogen and graphite nitrogen are involved in ORR as active sites, with pyridine nitrogen possessing a pair of lone electrons that can weaken the O−O bond of O 2 ; thus, it enhanced oxygen adsorption and exhibited better catalytic performance. 8, 45, 46, 59 It can be deduced that the synergistic effects between Co 2 P 2 O 7 /C and PANI-derived N,P−C with the active N species (pyridine N, and graphitic N) can effectively reduce the activation barrier of the adsorbed O 2 to promote the capture of the first electron to enhance the cleavage of O−O bonds, thereby improving the ORR activity. 60 Further, we can see that the specific surface area was also significantly affected through the PANI polarization time. All of the N 2 adsorption−desorption isotherms exhibit the II-type curve in Figure 9 , and the BET surface area is compiled in Table 3 . The Co 2 P 2 O 7 /C@N,P−C-3h catalyst possesses a surface area of 459.30 m 2 /g, which is approximately twice that of the Co 2 P 2 O 7 /C@N,P−C-4h catalyst, which possesses a surface area of 237.71 m 2 /g. The hierarchical porous structure is noticed with an average pore diameter of 4.63 nm in Co 2 P 2 O 7 /C@N,P−C. The hierarchical porous structure develops a specific surface area, which provides numerous energetic spots for the catalytic reaction; meanwhile, porosity facilitates the transfer of reactants, promotes the occurrence of catalytic response, and thus improves the catalytic ability (Figures 10 and 11 ).

Electrochemical impedance spectroscopy (EIS) measurement Nyquist diagram is one of the effective methods for measuring electrochemically active sites. The Nyquist diagram shows that the slope of the Co 2 P 2 O 7 /C@N,P−C-3h catalyst is larger than that of other samples, indicating faster kinetics of charge transfer and an increase in the ion diffusion rate.

We also compared the long-term electrochemical stability of Co 2 P 2 O 7 /C@N,P−C and 20% Pt/C catalysts. The i−t Figure 10 . (a) N 2 adsorption−desorption isotherms for Co 2 P 2 O 7 /C@N,P−C-3h, Co 2 P 2 O 7 /C@N,P−C-4h, and Co 2 P 2 O 7 /C@N,P−C-5h and (b) the corresponding pore diameter distribution diagram. Figure 11 . Nyquist plot of Co 2 P 2 O 7 /C@N,P−C-3h, Co 2 P 2 O 7 /C@ N,P−C-4h, and Co 2 P 2 O 7 /C@N,P−C-5h catalysts under 0.1 M KOH conditions.

http://pubs.acs.org/journal/acsodf Article response of Co 2 P 2 O 7 /C@N,P−C and Pt/C recorded for 8000 s at 500 rpm is shown in Figure 12 . The Co 2 P 2 O 7 /C@N,P−C catalyst exhibited better durability than the commercial Pt/C catalyst: only 9.1% of the activity was lost after 8000 s of a continuous ORR. For comparison, the commercial Pt/C catalyst demonstrated 7.7% lower activity after 8000 s.

To summarize, a simple hydrothermal technique and a subsequent pyrolysis strategy were used to synthesize N,Prich carbon/carbon Co 2 P 2 O 7 (Co 2 P 2 O 7 /C@N,P−C) tubular composite materials. The obtained Co 2 P 2 O 7 /C@N,P−C demonstrated a high catalytic activity toward the ORR due to the special hollowed structure and synergistic effect of the Co 2 P 2 O 7 and PANI-derived N,P-doped C. The onset and positive half-wave potentials were recorded at 0.90 and 0.84 V, respectively, while the diffusion-limited current density was 4.6 mA/cm 2 , values that were similar to those of commercial 20% Pt/C. The Co 2 P 2 O 7 /C@N,P−C catalyst also has excellent stability compared to 20% Pt/C. It was demonstrated that the specific surface area, as well as the content of graphitic N, changed with the time of PANI polymerization, resulting in a significantly different catalytic performance, and an optimal value was achieved with 3 h of PANI polymerization in its precursor. This investigation of hollow tube metal phosphatebased materials reveals significant potential for energy storage regeneration and conversion technologies. Long-term stability tests performed by the cathodic current−time (i−t) method using Co 2 P 2 O 7 /C@N,P−C and 20% Pt/ C catalyst performance during ORR.

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