Khan Karim, Tareen Ayesha Khan, Aslam Muhammad, Zhang Yupeng, Wang Renheng, Khan Sayed Ali, Khan Qudrat Ullah, Rauf Muhammad, Zhang Han, Ouyang Zhengbiao, Guo Zhongyi
School of Electrical Engineering & Intelligentization, Dongguan University of Technology (DGUT), Dongguan, China.
College of Electronic Science and Technology, THz Technical Research Center of Shenzhen University, Key Laboratory of Optoelectronics Devices and Systems of Ministry of Education and Guangdong Province Shenzhen University, Shenzhen, China.
Front Chem. 2020 Jan 22;7:934. doi: 10.3389/fchem.2019.00934. eCollection 2019.
This manuscript presented a large scale synthesis of Graphitic Shells like carbon nano onions (GS-CNOs) by direct solution method using mayenite electride as a catalyst for synthesis of CNOs. Thermal characterization, microstructural analysis, and high resolution electron microscopy have confirmed the graphitization and revealed the resulting GS-CNOs with particle size about 15 nm, maximum BET surface area of 214 m.g, and moderate conductivity of 250 S.cm, thus providing a new approach to synthesize GS-CNOs. The reported GS-CNOs, which acts as more active but less expensive electrocatalysts with onset potential of 1.03 V, half wave potential of 0.88 V vs. the reversible hydrogen electrode (RHE), and limited current density of 5.9 mA.cm, higher than that of benchmark 20% Pt/C (1.02 eV, 0.82 V, 5.2 mA.cm). The synthesized nano-powder acts as an origin of ORR activity via a four electron (4e) pathway, along with significantly enhanced stability, in alkaline media. The high ORR activity is ascribed to GS-CNOs embedded sufficient metallic C12A7:e particles, which favor faster electron movement and better adsorption of oxygen molecules on catalyst surface. Hence, we explored first time large scale synthesis of GS-CNOs with gram level and provide efficient approach to prepare novel, lowest cost, potential non-noble metals catalyst for fuel cells.
本手稿介绍了一种通过直接溶液法大规模合成类石墨壳碳纳米洋葱(GS-CNOs)的方法,该方法使用钙铝石电子化物作为合成CNOs的催化剂。热表征、微观结构分析和高分辨率电子显微镜证实了石墨化,并揭示了所得的GS-CNOs,其粒径约为15nm,最大BET表面积为214m²/g,电导率适中,为250S/cm,从而提供了一种合成GS-CNOs的新方法。报道的GS-CNOs作为更具活性但成本更低的电催化剂,相对于可逆氢电极(RHE)的起始电位为1.03V,半波电位为0.88V,极限电流密度为5.9mA/cm²,高于基准20%Pt/C(1.02eV,0.82V,5.2mA/cm²)。合成的纳米粉末在碱性介质中通过四电子(4e)途径作为氧还原反应(ORR)活性的来源,同时稳定性显著增强。高ORR活性归因于GS-CNOs中嵌入了足够的金属C12A7:e颗粒,这有利于更快的电子移动和氧分子在催化剂表面的更好吸附。因此,我们首次探索了克级规模的GS-CNOs大规模合成,并提供了一种有效的方法来制备用于燃料电池的新型、低成本、潜在的非贵金属催化剂。