Wan Zhongmin, Wang Linqing, Zhou Yuheng, Xu Siyuan, Zhang Jing, Chen Xi, Li Shi, Ou Changjie, Kong Xiangzhong
College of Mechanical Engineering, Hunan Institute of Science and Technology, Yueyang, 414006, China.
Institute of New Energy, Hunan Institute of Science and Technology, Yueyang, 414006, China.
Nanoscale. 2024 Mar 14;16(11):5845-5854. doi: 10.1039/d3nr06242b.
Anion exchange membrane water electrolysis (AEMWE) is considered one of the most cost-effective methods for producing green hydrogen. However, the performance of AEMWE is still restrained by the slow reaction kinetics and poor ion/electron transport of catalysts. Herein, inspired by frogspawn, MoC nanoparticles coupled with Ni were embedded into a N-doped porous carbon nanofiber network (MoC/NCNTs@Ni) by chemical crosslinking electrospinning combined with carbonization. The unique bionic structure can guarantee favorable overall structural flexibility and fast ion/electron transport kinetics. As a result of the robust hydrogen binding energy of MoC, as well as the synergistic impact between Ni and MoC nanoparticles and the conductive network resembling frogspawn, the catalyst developed demonstrates excellent performance in both the HER and OER. When employed as a bifunctional catalyst in water electrolysis, MoC/NCNTs@Ni delivers overpotentials of 155 mV and 320 mV at 10 mA cm for the HER and OER, respectively. In addition, the MoC/NCNTs@Ni also displays excellent long-term durability during a continuous operation test under different currents for 50 h. The assembled AEMWE electrolyzers with MoC/NCNTs@Ni as both the anode and cathode can achieve a current density of 82.5 mA cm at 1.99 V, indicating great potential for industrial water splitting. These results give an insight for the development of advanced bifunctional electrocatalysts for the next generation of green and efficient H production by water electrolysis.
阴离子交换膜水电解(AEMWE)被认为是生产绿色氢气最具成本效益的方法之一。然而,AEMWE的性能仍然受到催化剂反应动力学缓慢和离子/电子传输性能差的限制。在此,受蛙卵启发,通过化学交联静电纺丝结合碳化将碳化钼纳米颗粒与镍嵌入到氮掺杂多孔碳纳米纤维网络(MoC/NCNTs@Ni)中。独特的仿生结构可确保良好的整体结构柔韧性和快速的离子/电子传输动力学。由于碳化钼具有强大的氢结合能,以及镍与碳化钼纳米颗粒之间的协同作用以及类似蛙卵的导电网络,所开发的催化剂在析氢反应(HER)和析氧反应(OER)中均表现出优异的性能。当用作水电解中的双功能催化剂时,MoC/NCNTs@Ni在10 mA cm下HER和OER的过电位分别为155 mV和320 mV。此外,MoC/NCNTs@Ni在不同电流下连续运行50小时的测试中也表现出优异的长期耐久性。以MoC/NCNTs@Ni作为阳极和阴极组装的AEMWE电解槽在1.99 V下可实现82.5 mA cm的电流密度,表明其在工业水分解方面具有巨大潜力。这些结果为开发用于下一代绿色高效水电解制氢的先进双功能电催化剂提供了思路。