Department of Chemistry, Merkert Chemistry Center, Boston College, Chestnut Hill, Massachusetts 02467, United States.
J Am Chem Soc. 2012 Mar 28;134(12):5508-11. doi: 10.1021/ja300319g. Epub 2012 Mar 13.
Mg-doped hematite (α-Fe(2)O(3)) was synthesized by atomic layer deposition (ALD). The resulting material was identified as p-type with a hole concentration of ca. 1.7 × 10(15) cm(-3). When grown on n-type hematite, the p-type layer was found to create a built-in field that could be used to assist photoelectrochemical water splitting reactions. A nominal 200 mV turn-on voltage shift toward the cathodic direction was measured, which is comparable to what has been measured using water oxidation catalysts. This result suggests that it is possible to achieve desired energetics for solar water splitting directly on metal oxides through advanced material preparations. Similar approaches may be used to mitigate problems caused by energy mismatch between water redox potentials and the band edges of hematite and many other low-cost metal oxides, enabling practical solar water splitting as a means for solar energy storage.
镁掺杂赤铁矿(α-Fe(2)O(3))通过原子层沉积(ALD)合成。所得材料被鉴定为 p 型,空穴浓度约为 1.7×10(15)cm(-3)。当在 n 型赤铁矿上生长时,发现 p 型层会产生内置电场,可用于辅助光电化学水分解反应。测量到约 200 mV 的正向电压向阴极方向的偏移,这与使用水氧化催化剂所测量的值相当。这一结果表明,通过先进的材料制备,有可能直接在金属氧化物上实现太阳能水分解所需的能量学。类似的方法可用于缓解水氧化还原电位与赤铁矿和许多其他低成本金属氧化物能带边缘之间的能量不匹配所引起的问题,使实际的太阳能水分解成为太阳能储存的一种手段。