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首页> 外文期刊>Nanoscale >Hydrochloric acid corrosion induced bifunctional free-standing NiFe hydroxide nanosheets towards high-performance alkaline seawater splitting
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Hydrochloric acid corrosion induced bifunctional free-standing NiFe hydroxide nanosheets towards high-performance alkaline seawater splitting

机译:盐酸腐蚀诱导双官能独立的镍铁氢氧化物nanosheets方向高性能碱性海水分裂

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We report a facile route to fabricate free-standing NiFe hydroxides by corrosion engineering as high-performance bifunctional electrocatalysts for seawater splitting. Compared with H2SO4 and HNO3, HCl can promote the dissolution of Ni2+ from NiFe foam and the in situ formation of active NiFe hydroxides due to the strong interaction between Cl- and metal. In situ Raman spectroscopic characterization reveals that HCl corrosion induced NiFe hydroxides (HCl-c-NiFe) can generate oxygen evolution reaction (OER) active NiOOH species at a low potential of 1.4 V vs. reversible hydrogen electrode (RHE) and exhibits equally respectable activity for the hydrogen evolution reaction (HER). During a 1000 h test in an alkaline electrolyte or a 300 h test in an alkaline seawater electrolyte within a two-electrode system at 100 mA cm(-2), the cell exhibits outstanding stability and high Cl- tolerance with a low working voltage of 1.62 V, outperforming benchmark Pt/IrO2 and most of the reported bifunctional catalysts.
机译:我们报告一个灵巧的制造独立的镍铁氢氧化物的腐蚀工程作为高性能双官能electrocatalysts海水分裂。盐酸和硫酸和硝酸,可以推广解散Ni2 +泡沫镍铁和原位形成活性镍铁的氢氧化物由于氯离子和金属之间的强相互作用。原位拉曼光谱表征,盐酸腐蚀引起镍铁氢氧化物进化(HCl-c-NiFe)可以生成氧气反应(OER)活跃NiOOH物种低1.4 V的潜力与可逆氢电极(流值)和展品同样值得尊敬析氢反应活动(她)。在碱性电解液或300 h测试海水在二电极电解液系统(2)马在100厘米,细胞展品出色的稳定性和高Cl -宽容低工作电压1.62 V,超越基准Pt / IrO2和大部分的报道双功能催化剂。

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