Chen Yuehan, Wang Shuping, Li Zhoupeng
Zhejiang Provincial Key Laboratory of Advanced Chemical Engineering Manufacture Technology, Zhejiang University Hangzhou 310027 China
College of Chemical and Biological Engineering, Zhejiang University Hangzhou 310027 China.
RSC Adv. 2020 Aug 6;10(49):29119-29127. doi: 10.1039/d0ra05143h. eCollection 2020 Aug 5.
Pyrrole and cobalt nitrate were used as nitrogen and metal sources respectively to synthesize a dinitratobis(polypyrrole)cobalt(ii) (Co(polypyrrole)(NO)) adduct as the precursor of a Co-pyrrole/MPC catalyst. Pyrrole has the capability of polymerization and coordination with Co(ii). Taking this advantage, the Co(polypyrrole)(NO) coordination can form a long-chain structure with abundant and robust Co-N bonds, contributing to significantly increased catalytic sites in the product catalyst. As a result, the obtained Co-pyrrole/MPC (MPC = macroporous carbon) catalyst exhibited high ORR catalytic activity in alkaline media and excellent performance in direct borohydride fuel cell (DBFC). A peak power density up to 325 mW cm was achieved at ambient condition, outperforming the commercialized Pt/XC-72 benchmark containing 28.6 wt% Pt. The construction of long-chain coordination precursor was verified playing a key role in the electrochemical improvement of Co-pyrrole/MPC catalyst in DBFC.
吡咯和硝酸钴分别用作氮源和金属源,以合成二硝酸双(聚吡咯)钴(II)(Co(聚吡咯)(NO))加合物作为Co-吡咯/MPC催化剂的前体。吡咯具有聚合能力以及与Co(II)配位的能力。利用这一优势,Co(聚吡咯)(NO)配位可形成具有丰富且稳定的Co-N键的长链结构,有助于显著增加产物催化剂中的催化位点。结果,所制备的Co-吡咯/MPC(MPC = 大孔碳)催化剂在碱性介质中表现出高ORR催化活性,在直接硼氢化物燃料电池(DBFC)中具有优异性能。在环境条件下实现了高达325 mW cm的峰值功率密度,优于含有28.6 wt% Pt的商业化Pt/XC-72基准材料。长链配位前体的构建被证实对DBFC中Co-吡咯/MPC催化剂的电化学性能提升起着关键作用。