Öztürk Secil, Xiao Yu-Xuan, Dietrich Dennis, Giesen Beatriz, Barthel Juri, Ying Jie, Yang Xiao-Yu, Janiak Christoph
Institut für Anorganische Chemie und Strukturchemie, Heinrich-Heine-Universität Düsseldorf, 40204 Düsseldorf, Germany.
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and School of Materials Science and Engineering, Wuhan University of Technology, 430070 Wuhan, China.
Beilstein J Nanotechnol. 2020 May 11;11:770-781. doi: 10.3762/bjnano.11.62. eCollection 2020.
Covalent triazine frameworks (CTFs) are little investigated, albeit they are promising candidates for electrocatalysis, especially for the oxygen evolution reaction (OER). In this work, nickel nanoparticles (from Ni(COD)) were supported on CTF-1 materials, which were synthesized from 1,4-dicyanobenzene at 400 °C and 600 °C by the ionothermal method. CTF-1-600 and Ni/CTF-1-600 show high catalytic activity towards OER and a clear activity for the electrochemical oxygen reduction reaction (ORR). Ni/CTF-1-600 requires 374 mV overpotential in OER to reach 10 mA/cm, which outperforms the benchmark RuO catalyst, which requires 403 mV under the same conditions. Ni/CTF-1-600 displays an OER catalytic activity comparable with many nickel-based electrocatalysts and is a potential candidate for OER. The same Ni/CTF-1-600 material shows a half-wave potential of 0.775 V for ORR, which is slightly lower than that of commercial Pt/C (0.890 V). Additionally, after accelerated durability tests of 2000 cycles, the material showed only a slight decrease in activity towards both OER and ORR, demonstrating its superior stability.
共价三嗪框架(CTFs)虽然是电催化尤其是析氧反应(OER)的有前途的候选材料,但目前对其研究较少。在这项工作中,镍纳米颗粒(来自Ni(COD))负载在CTF-1材料上,CTF-1材料是由1,4-二氰基苯在400℃和600℃通过离子热法合成的。CTF-1-600和Ni/CTF-1-600对OER表现出高催化活性,对电化学氧还原反应(ORR)也有明显活性。Ni/CTF-1-600在OER中达到10 mA/cm²需要374 mV的过电位,优于基准RuO₂催化剂,后者在相同条件下需要403 mV。Ni/CTF-1-600的OER催化活性与许多镍基电催化剂相当,是OER的潜在候选材料。相同的Ni/CTF-1-600材料在ORR中的半波电位为0.775 V,略低于商业Pt/C(0.890 V)。此外,经过2000次循环的加速耐久性测试后,该材料对OER和ORR的活性仅略有下降,表明其具有优异的稳定性。