Jin Zhaoyu, Li Panpan, Xiao Dan
Key Laboratory of Green Chemistry and Technology, Ministry of education, College of Chemistry, Sichuan University, Chengdu 610064, P. R. China.
1] Key Laboratory of Green Chemistry and Technology, Ministry of education, College of Chemistry, Sichuan University, Chengdu 610064, P. R. China [2] College of Architecture and Environment, Sichuan University, Chengdu 610065, P. R. China.
Sci Rep. 2014 Oct 22;4:6712. doi: 10.1038/srep06712.
Cathode materials always limit the performance of fuel cells while the commercial platinum-based catalysts hardly meet the requirements of low cost, durable and stable. Here a non-precious metal oxygen reduction reaction (ORR) electocatalyst based on titanium nitride/titanium carbonitride hierarchical structures (TNTCNHS) is demonstrated as high activity as Pt/C. In alkaline condition, tuning interface/mass ratio of TiN/TiCN, we observed the onset potential of ~0.93 V vs. RHE and a limit diffusion current density of ~5.1 mA cm(-2) (at a rotating speed of 1600 rpm) on TNTCNHS with a relative low catalyst loading of ~0.1 mg cm(-2). The kinetic current, durability and tolerance to crossover effect studies reveal even more efficient than carbon-supported platinum. The architecture fabrication for such electrocatalyst is easy to realize in industrial-scale facilities, for the use of chemical vapor deposition (CVD) technique could support a huge area production (more than 10000 cm(2) for one pot) to satisfy the enormous market requirements in the future.
阴极材料一直限制着燃料电池的性能,而商业化的铂基催化剂很难满足低成本、耐用和稳定的要求。在此,一种基于氮化钛/碳氮化钛分级结构(TNTCNHS)的非贵金属氧还原反应(ORR)电催化剂被证明具有与Pt/C一样高的活性。在碱性条件下,通过调整TiN/TiCN的界面/质量比,我们在TNTCNHS上观察到相对于可逆氢电极(RHE)约0.93 V的起始电位和约5.1 mA cm(-2)的极限扩散电流密度(在1600 rpm的转速下),且催化剂负载相对较低,约为0.1 mg cm(-2)。动力学电流、耐久性和对交叉效应的耐受性研究表明,该催化剂甚至比碳载铂更高效。这种电催化剂的结构制造在工业规模的设施中很容易实现,因为化学气相沉积(CVD)技术的使用能够支持大面积生产(一锅法可生产超过10000 cm(2)),以满足未来巨大的市场需求。