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Pushing the limits for enzyme-based membrane-less hydrogen fuel cells – achieving useful power and stability

机译:推动基于酶的膜的氢燃料电池的限制 - 实现有用的功率和稳定性

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The performance characteristics of simple enzyme-based membrane-less hydrogen fuel cells running on non-explosive H _(2) -rich air mixtures have been established using an adjustable test bed that allows multiple unit cells to operate in series or parallel. Recent advances with ‘3D’ electrodes constructed from compacted porous carbon loaded with hydrogenase (anode) and bilirubin oxidase (cathode) have been extended in order to scale up fuel cell power to useful levels. One result is an appealing ‘classroom’ demonstration of a model house containing small electronic devices powered by H _(2) mixed with a small amount of air. The 3D electrodes work by greatly increasing catalyst loading (at both the anode and cathode) and selectively restricting the access of O _(2) (relative to H _(2) ) to enzymes embedded in pores at the anode. The latter property raises the possibility of using standard hydrogenases that are not O _(2) -tolerant: however, experiments with such an enzyme reveal good short-term performance due to restricted O _(2) access, but low long-term stability because the root cause of O _(2) sensitivity has not been addressed. Hydrogenases that are truly O _(2) tolerant must therefore remain the major focus of any future enzyme-based hydrogen fuel cell technology.
机译:使用可调节试验台建立了在非爆炸性H _(2) - 中间空气混合物上运行的简单酶的膜的耐氢燃料电池的性能特征已经建立了可调节的试验台,其允许多个单元电池串联或并联操作。已经延长了由压实多孔碳(阳极)和胆红素氧化酶(阴极)的压实多孔碳构成的“3D”电极的前进的延伸,以便向上扩大燃料电池功率为有用的水平。一个结果是一个有吸引力的“教室”示范,其模型房屋包含由H _(2)和少量空气混合的小型电子设备。 3D电极通过大大增加催化剂负载(在阳极和阴极上),并选择性地限制O _(2)的进入(相对于H _(2))嵌入阳极处的孔中的酶。后一种特性提高了使用不o _(2) - 促议症的标准氢酶的可能性:然而,由于限制的O _(2)访问,但长期稳定性低,因此具有这种酶的实验显示出良好的短期性能,但长期稳定性低因为尚未解决O_(2)敏感性的根本原因。因此,真正o _(2)耐受的氢酶必须仍然是任何未来酶的氢燃料电池技术的主要焦点。

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