| Project/Area Number |
17H01229
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Inorganic industrial materials
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| Research Institution | University of Yamanashi |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
柿沼 克良 山梨大学, 大学院総合研究部, 特任教授 (60312089)
A.TRYK Donald 山梨大学, 大学院総合研究部, 特任教授 (30530092)
野原 愼士 山梨大学, 大学院総合研究部, 准教授 (40326278)
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| Project Period (FY) |
2017-04-01 – 2020-03-31
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| Project Status |
Completed (Fiscal Year 2019)
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| Budget Amount *help |
¥44,200,000 (Direct Cost: ¥34,000,000、Indirect Cost: ¥10,200,000)
Fiscal Year 2019: ¥11,960,000 (Direct Cost: ¥9,200,000、Indirect Cost: ¥2,760,000)
Fiscal Year 2018: ¥15,600,000 (Direct Cost: ¥12,000,000、Indirect Cost: ¥3,600,000)
Fiscal Year 2017: ¥16,640,000 (Direct Cost: ¥12,800,000、Indirect Cost: ¥3,840,000)
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| Keywords | 固体高分子形水電解 / 水素製造 / 電極触媒 / 水素 / 構造・機能材料 / ナノ材料 / エネルギー効率化 / 新エネルギー |
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| Outline of Final Research Achievements |
We investigated low noble-metal electrocatalysts and catalyst layers for polymer electrolyte water electrolyzers to produce H2 efficiently. IrOx nanoparticles (ca. 2 nm) dispersed on M-SnO2 (M=Nb, Ta, Sb) support with a fused-aggregate structure exhibited higher mass activity (MA, by 27 to 36 times) for the O2 evolution than that of conventional (IrO2+Pt) black, due to a large active area and the interaction with the support. A single cell with IrOx/Sb-SnO2 anode and Pt/GCB cathode showed 92% voltage efficiency even with 1/10 noble-metal loading.
A heat-treated Pt3Co/C cathode catalyst exhibited 4 timer higher MA for the H2 evolution than that of commercial Pt/C. We clarified the mechanism for the enhanced activity by using Pt3Co single crystal electrodes. It was found that Pt skin－PtFe/C catalyst suppressed a formation rate of H2O2, which induces a decomposition of polymer electrolytes. A single cell with Pt skin－PtFe/C cathode (1/10 Pt loading) operated stably for 1000 h.
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| Academic Significance and Societal Importance of the Research Achievements |
貴金属量を従来の1/10に低減可能な酸素発生触媒と水素発生触媒の合成法を確立し、活性増大機構と設計指針を明らかにしたことは、材料科学、触媒化学、電気化学の今後の発展に大きく貢献する。貴金属量を1/10に低減した固体高分子形水電解で90%以上の高効率で水素製造が可能なことを実験により示したことは、学術的にも社会的にも意義は大きい。また、高分子電解質膜の化学劣化源となるH2O2生成を抑制する水素発生触媒の開発により、電解質膜を薄膜化しても耐久性が保てるため、性能と耐久性の両立が可能になる。この成果は、学術面と実用面で大きな進歩である。
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