Soto-Pérez Joesene, Betancourt Luis E, Trinidad Pedro, Larios Eduardo, Rojas-Pérez Arnulfo, Quintana Gerardo, Sasaki Kotaro, Pollock Christopher J, Debefve Louise M, Cabrera Carlos R
Department of Chemistry, University of Puerto Rico, Río Piedras Campus, San Juan 00925-2537, Puerto Rico.
Chemistry Division, Brookhaven National Laboratory, Upton, New York 11973, United States.
ACS Omega. 2021 Jul 1;6(27):17203-17216. doi: 10.1021/acsomega.1c00792. eCollection 2021 Jul 13.
Studying the oxygen reduction reaction (ORR) in the alkaline electrolyte has proven to promote better catalytic responses and accessibility to commercialization. Ni-nanowires (NWs) were synthesized via the solvothermal method and modified with Pt using the spontaneous galvanic displacement method to obtain PtNi-NWs. Carbon Vulcan XC-72R (V) was used as the catalyst support, and they were doped with NH to obtain PtNi-NWs/V and PtNi-NWs/V-NH. Their electrocatalytic response for the ORR was tested and PtNi-NWs/V provided the highest specific activity with logarithmic values of 0.707 and 1.01 (mA/cm ) at 0.90 and 0.85 V versus reversible hydrogen electrode (RHE), respectively. PtNi-NWs showed the highest half-wave potential ( = 0.89 V) at 1600 rpm and 12 μg/cm in 0.1 M KOH at 25.00 ± 0.01 °C. Additionally, the catalysts followed a four-electron pathway according to the Koutecký-Levich analysis. Moreover, durability experiments demonstrated that the PtNi-NW/V performance loss was like that of commercial Pt/V along 10,000 cycles. Electrochemical ORR X-ray absorption spectroscopy results showed that the Pt L edge white line in the PtNi-NW catalysts changed while the electrochemical potential was lowered to negatives values, from 1.0 to 0.3 V versus RHE. The Pt/O region in the Fourier transforms remained the same as the potentials were applied, suggesting an alloy formation between Pt and Ni, and Pt/Pt contracted in the presence of Ni. These results provide a better understanding of PtNi-NWs in alkaline electrolytes, suggesting that they are active catalysts for ORR and can be tuned for fuel cell studies.
研究碱性电解质中的氧还原反应(ORR)已被证明能促进更好的催化反应并推动商业化进程。通过溶剂热法合成了镍纳米线(NWs),并使用自发电置换法用铂对其进行改性,以获得铂镍纳米线。采用碳Vulcan XC - 72R(V)作为催化剂载体,并对其进行氮掺杂以获得铂镍纳米线/V和铂镍纳米线/V - N。测试了它们对ORR的电催化响应,铂镍纳米线/V在相对于可逆氢电极(RHE)为0.90和0.85 V时分别提供了最高的比活性,对数数值为0.707和1.01(mA/cm²)。在25.00±0.01°C、0.1 M KOH中,转速为1600 rpm且载量为12 μg/cm²时,铂镍纳米线显示出最高的半波电位(E1/2 = 0.89 V)。此外,根据Koutecký - Levich分析,这些催化剂遵循四电子途径。而且,耐久性实验表明,在10,000次循环中,铂镍纳米线/ V的性能损失与商业铂/ V相当。电化学ORR X射线吸收光谱结果表明,当电化学电位从相对于RHE的1.0 V降低到负值0.3 V时,铂镍纳米线催化剂中的铂L边白线发生了变化。施加电位时,傅里叶变换中的Pt/O区域保持不变,这表明铂和镍之间形成了合金,并且在镍存在的情况下Pt/Pt峰变窄。这些结果有助于更好地理解碱性电解质中的铂镍纳米线,表明它们是ORR的活性催化剂,可用于燃料电池研究的优化。