Construction of superhydrophilic FeP–Ni2P–CoP/NF enriched interfacial heterostructures for promoting efficient and stable overall water splitting under large currents†
Yaxuan Jin, Weiyan Ma, Dong Sun, Wan Wan, Lirong Jia, Yuling Tu, Dejun Gong, Wanyong Zhou and Hui Chai
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引用次数: 0
Abstract
It is of great importance to devise highly effective and durable non-precious metal catalysts capable of operating at high current densities, in order to cater to the requirements of practical applications. Here, FeP–Ni2P–CoP heterostructured catalysts grown on NF (Ni foam) were prepared by a simple one-step hydrothermal and low-temperature phosphatization strategy. The optimized FeP–Ni2P–CoP/NF catalysts exhibited excellent catalytic activity in the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The HER and OER overpotentials are 128 mV and 256 mV at 100 mA cm−2, and high current densities of 500 mA cm−2 can be achieved with only 190 mV and 288 mV. Impressively, the electrolyzer requires only an ultra-low cell voltage of 1.5 V to reach 10 mA cm−2. In addition, the catalyst was able to operate stably at a high current density of 1000 mA cm−2 for 500 hours. This is mainly attributed to the heterogeneous structure of FeP–Ni2P–CoP/NF nanowires, which exposes more active area, accelerates ionic transport and bubble release, and alters the local electronic structure of the interface, thereby improving its hydrophilicity and enhancing the intrinsic activity and stability. This work provides new ideas for the use of polymetallic-based phosphides for overall water decomposition at high current densities.
为了满足实际应用的需要,设计出高效、耐用且能在高电流密度下工作的非贵金属催化剂具有重要意义。本文采用简单的一步水热和低温磷化策略,在NF (Ni泡沫)上制备了FeP-Ni2P-CoP异质结构催化剂。优化后的FeP-Ni2P-CoP /NF催化剂在析氢反应(HER)和析氧反应(OER)中表现出优异的催化活性。在100 mA cm - 2时,HER和OER过电位分别为128 mV和256 mV,在190 mV和288 mV时可达到500 mA cm - 2的高电流密度。令人印象深刻的是,电解槽只需要1.5 V的超低电池电压就可以达到10 mA cm - 2。此外,该催化剂能够在1000 mA cm−2的高电流密度下稳定工作500小时。这主要是由于FeP-Ni2P-CoP /NF纳米线的非均相结构使其暴露出更多的活性区域,加速了离子传递和气泡释放,改变了界面的局部电子结构,从而提高了其亲水性,增强了其固有活性和稳定性。这项工作为在高电流密度下使用多金属基磷化物进行整体水分解提供了新的思路。