Wu Yu-Lin, Li Xiaofang, Wei Yong-Sheng, Fu Zhaoming, Wei Wenbo, Wu Xin-Tao, Zhu Qi-Long, Xu Qiang
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences (CAS), Fuzhou, 350002, China.
AIST-Kyoto University Chemical Energy Materials Open Innovation Laboratory (ChEM-OIL), National Institute of Advanced Industrial Science and Technology (AIST), Sakyo-ku, Kyoto, 6068501, Japan.
Adv Mater. 2021 Mar;33(12):e2006965. doi: 10.1002/adma.202006965. Epub 2021 Feb 18.
The electrochemical hydrogen evolution reaction (HER) is an attractive technology for the mass production of hydrogen. Ru-based materials are promising electrocatalysts owing to the similar bonding strength with hydrogen but much lower cost than Pt catalysts. Herein, an ordered macroporous superstructure of N-doped nanoporous carbon anchored with the ultrafine Ru nanoclusters as electrocatalytic micro/nanoreactors is developed via the thermal pyrolysis of ordered macroporous single crystals of ZIF-8 accommodating Ru(III) ions. Benefiting from the highly interconnected reticular macro-nanospaces, this superstrucure affords unparalleled performance for pH-universal HER, with order of magnitude higher mass activity compared to the benchmark Pt/C. Notably, an exceptionally low overpotential of only 13 mV@10 mA cm is required for HER in alkaline solution, with a low Tafel slope of 40.41 mV dec and an ultrahigh turnover frequency value of 1.6 H s at 25 mV, greatly outperforming Pt/C. Furthermore, the hydrogen generation rates are almost twice those of Pt/C during practical overall alkaline water splitting. A solar-to-hydrogen system is also demonstrated to further promote the application. This research may open a new avenue for the development of advanced electrocatalytic micro/nanoreactors with controlled morphology and excellent performance for future energy applications.
电化学析氢反应(HER)是一种极具吸引力的大规模制氢技术。钌基材料因其与氢的键合强度相似但成本远低于铂催化剂,是很有前景的电催化剂。在此,通过对容纳Ru(III)离子的ZIF-8有序大孔单晶进行热解,制备了一种以超细Ru纳米团簇为电催化微/纳米反应器的N掺杂纳米多孔碳有序大孔超结构。受益于高度互连的网状宏观-纳米空间,这种超结构在pH通用的HER中表现出无与伦比的性能,与基准Pt/C相比,质量活性高出一个数量级。值得注意的是,在碱性溶液中HER仅需13 mV@10 mA cm的极低过电位,Tafel斜率低至40.41 mV dec,在25 mV时的超高周转频率值为1.6 H s,大大优于Pt/C。此外,在实际的全碱性水分解过程中,产氢速率几乎是Pt/C的两倍。还展示了一个太阳能制氢系统以进一步推动其应用。这项研究可能为开发具有可控形态和优异性能的先进电催化微/纳米反应器开辟一条新途径,以用于未来的能源应用。