Abstract:Bi–CoP nanoparticles supported on N, P doped defective graphene aerogel (Bi–CoP–P-DG) electrocatalyst presents excellent catalytic performances for OER, ORR and Zn–air battery. Moreover, the home-made Zn–air battery can drive overall water-splitting.
Herein, Co/CoP nanoparticles encapsulated with N, P-doped carbon nanotubes derived from the atomic layer deposited hexagonal metal-organic frameworks (MOFs) are obtained by calcinations and subsequent phosphating and are employed as electrocatalyst. The electrocatalytic performance evaluations show that the as-prepared electrocatalyst exhibits an overpotential of 342 mV at current density of 10 mA cm −2 and the Tafel slope of 74 mV dec −1 for oxygen evolution reaction (OER), which is superior to the most advanced ruthenium oxide electrocatalyst. The electrocatalyst also shows better stability than the benchmark RuO 2. After 9 h, the current density is only decreased by 10%, which is far less than the loss of RuO 2. Moreover, its onset potential for oxygen reduction reaction (ORR) is 0.93 V and follows the ideal 4-electron approach. After the stability test, the current density of the electrocatalyst retains 94% of the initial value, which is better than Pt/C. The above results indicate that the electrocatalyst has bifunctional activity and excellent stability both for OER and ORR. It is believed that this strategy provides guidance for the synthesis of cobalt phosphide/carbon-based electrocatalysts.
Herein, Co/CoP nanoparticles encapsulated with N, P-doped carbon nanotubes derived from the atomic layer deposited hexagonal metal-organic frameworks (MOFs) are obtained by calcinations and subsequent phosphating and are employed as electrocatalyst. The electrocatalytic performance evaluations show that the as-prepared electrocatalyst exhibits an overpotential of 342 mV at current density of 10 mA cm −2 and the Tafel slope of 74 mV dec −1 for oxygen evolution reaction (OER), which is superior to the most advanced ruthenium oxide electrocatalyst. The electrocatalyst also shows better stability than the benchmark RuO 2. After 9 h, the current density is only decreased by 10%, which is far less than the loss of RuO 2. Moreover, its onset potential for oxygen reduction reaction (ORR) is 0.93 V and follows the ideal 4-electron approach. After the stability test, the current density of the electrocatalyst retains 94% of the initial value, which is better than Pt/C. The above results indicate that the electrocatalyst has bifunctional activity and excellent stability both for OER and ORR. It is believed that this strategy provides guidance for the synthesis of cobalt phosphide/carbon-based electrocatalysts.
“…The slope of Ni 3 S 2 -350 °C in Figure a is higher than that of the other samples, indicating that it has a very large specific surface area. Because the slope is larger, the roughness of the material itself is larger, indicating that the catalyst has a large active area, which reflects the catalytic performance of the material. , Figure b shows the Mott–Schottky (M-S) curves of different Ni 3 S 2 NR samples. The donor N D and acceptor N A concentration can be obtained by fitting the following Mott–Schottky equation where ε sc , ε 0 , N D , N A , C SC , V , V fb , and q are the dielectric constant of the semiconductor, the vacuum permittivity (8.86 × 10 –14 F cm –1 ), the donor concentration, acceptor concentration, the capacitance of the space charge layer, the applied potential, the flat band potential, and the charge constant (1.6 × 10 –19 C), respectively.…”
Rationally designing a new type of earth-abundant and environmentally friendly material with high performance and durability that can convert water to energy by the control point defect method is still a challenge. Herein, we report a newly adjusted method to prepare Ni 3 S 2 nanorods (NRs) by combining transition metals and nanostructures while introducing sulfur vacancies as a means of promoting electron−hole pair transfer. It shows excellent hydrogen evolution electrocatalytic (HER) activity with an overpotential of 162 mV at j = 10 mA cm −2 and chemical stability in 1 M NaOH solution. Electrochemically active surface area (ECSA) calculation results of 0.36 m 2 g −1 confirm the superior performance of Ni 3 S 2 with sulfur vacancies compared to other materials. The Mott−Schottky (M-S) and electrochemical impedance spectroscopy (EIS) results allowed effective optimization of the nanorods after obtaining sulfur vacancies and, surprisingly, showed that they are a P/N-type semiconductor. We speculate that the HER of the Ni 3 S 2 NRs is mainly dominated by the Heyrovsky process. At the same time, the synergistic reaction produced by the electron−hole transfer guided by sulfur vacancies promotes the Heyrovsky process, thus jointly improving the effectiveness of the Ni 3 S 2 NRs. The method of introducing sulfur vacancies in the nanomaterial is simple and has excellent properties, which suggests broad applications for research in the fields of environment and energy.
“…All these merits make Zn‐air battery become a feasible power supply compared with other contenders [12–16] . In Zn‐air battery, discharge of cathode is realized by oxygen reduction reaction (ORR, O 2 +2H 2 O+4e↔4OH − ) [17–21] . During charge process, oxygen evolution reaction happens (OER, 4OH − −4e↔O 2 +2H 2 O) [22–25] .…”
Zn‐air batteriesare a perspective power source for grid‐storage. But, after they are discharged at1.1 to 1.2 V, large overpotential is required for their charging (usually 2.5 V). This is due to a sluggish oxygen evolution reaction (OER). Incorporating organic pollutants into the cathode electrolyte is a feasible strategy for lowering the required charging potential. In the discharge process, the related oxygen reduction reaction, hydrophobic electrocatalysts are more popular than hydrophilic ones. Here, a hydrophobic bifunctional polyoxometalate electrocatalyst is synthesized by precise structural design. It shows excellent activities in both bisphenol A degradation and oxygen reduction reactions. In bisphenol A containing electrolyte, to achieve 100 mA ⋅ cm−2, its potential is only 1.32 V, which is 0.34 V lower than oxygen evolution reaction. In the oxygen reduction reaction, this electrocatalyst follows the four‐electron mechanism. In both bisphenol A degradation and oxygen reduction reactions, it shows excellent stability. With this electrocatalyst as cathode material and bisphenol A containing KOH as electrolyte, a Zn‐air battery was assembled. When “charged” at 85 mA ⋅ cm−2, it only requires 1.98 V. Peak power density of this Zn‐air battery reaches 120.5 mW ⋅ cm−2. More importantly, in the “charge” process, bisphenol A is degraded, which achieves energy saving and pollutant removal simultaneously in one Zn‐air battery.
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