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Unique amorphous/crystalline heterophase coupling for an efficient oxygen evolution reaction

机译:独特的无定形/结晶异相偶联,可实现高效的析氧反应

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摘要

Designing amorphous/crystalline heterophase catalysts is still in the initial stage, and the study of amorphous/crystalline heterophase and carbon-free catalysts has not yet been realized. Herein, we report a unique amorphous/crystalline heterophase catalyst consisting of NiFe alloy nanoparticles (NPs) supported on Ti4O7 (NiFe/Ti4O7) for the first time, which is achieved by a heterophase supporting strategy of dual heat treatment. Surprisingly, the amorphous/crystalline heterophase is flexibly composed of amorphous and crystalline phases of alloy NPs and Ti4O7. The heterophase coupling endows the catalyst with a low overpotential (256 mV at 10 mA cm−2), a small Tafel slope (47 mV dec−1) and excellent endurance stability (over 100 h) in 1 M KOH electrolyte, which already outperforms commercial RuO2 (338 mV and 113 mV dec−1) and exceeds most reported representative carbon-based and titanium-based non-precious metal catalysts. The density functional theory (DFT) calculations and experimental results reveal that the unique amorphous/crystalline heterophase coupling in NiFe/Ti4O7 results in electron transfer between the alloy NPs and Ti4O7, allowing more catalytically active sites and faster interfacial electron transfer dynamics. This work provides insights into the synthesis of amorphous/crystalline heterophase catalysts and can be generalized to the heterophase coupling of other transition metal-based electrocatalysts.
机译:设计非晶/水晶多相催化剂仍处于初始阶段,研究非晶/水晶多相和无碳催化剂尚未实现。在此,我们报告一个独特的非晶/水晶多相催化剂镍铁组成的合金Ti4O7纳米颗粒(NPs)支持(镍铁/ Ti4O7)第一次,这是通过一个多相支持的策略双重热处理。非晶/水晶多相灵活由无定形和结晶阶段合金NPs Ti4O7。赋予催化剂低过电压(256mV马10厘米−2),一个小塔费尔斜率(47 mV12月−1)和优秀的耐力(超过稳定100 h)在1 M KOH电解质优于商业RuO2 (338 mV和113 mV12月−1)和超过大多数报道的代表碳和种钛non-precious金属催化剂。(DFT)计算和实验结果显示独特的非晶/水晶多相耦合在镍铁/ Ti4O7结果合金NPs和之间的电子转移Ti4O7,允许更多的催化地活跃的网站和更快的界面电子转移动力学。合成的非晶/水晶多相催化剂和推广多相耦合的过渡金属electrocatalysts。

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